diff --git a/lib/import/brca/providers/st_george_old/st_george_handler_old.rb b/lib/import/brca/providers/st_george_old/st_george_handler_old.rb
index 171c74c9..b857ec32 100644
--- a/lib/import/brca/providers/st_george_old/st_george_handler_old.rb
+++ b/lib/import/brca/providers/st_george_old/st_george_handler_old.rb
@@ -11,7 +11,8 @@ class StGeorgeHandlerOld < Import::Germline::ProviderHandler
           PASS_THROUGH_FIELDS = %w[age sex consultantcode collecteddate
                                    receiveddate authoriseddate servicereportidentifier
                                    providercode receiveddate sampletype].freeze
-          CDNA_REGEX = /c\.(?<cdna>[0-9]+[^\s)]+)|c\.\[(?<cdna>.*?)\]/i.freeze
+          CDNA_REGEX = /c\.(?<cdna>[0-9]+[^\s)]+)|c\.\[(?<cdna>.*?)\]|c\.\*(?<cdna>[0-9]+[^\s)]+)/i.freeze
+
 
           PROTEIN_REGEX = /p\.(?<impact>[a-z]+[0-9]+[a-z]+)|
                            p\.(?<sqrbo>\[)?(?<rndbo>\()?(?<impact>[a-z]+[0-9]+[a-z]+)
@@ -47,7 +48,9 @@ class StGeorgeHandlerOld < Import::Germline::ProviderHandler
                               (?<exons>[0-9]+(?<dgs>\sto\s[0-9]+))|
                               (?<variant>del|dup|ins)(?<s>\s)?(?<exons>[0-9]+(?<dgs>-[0-9]+)?)|
                               ex(?<on>on)?(?<s>s)?\s(?<exons>[0-9]+(?<dgs>\sto\s[0-9]+)?)\s
-                              (?<variant>del|dup|ins)/ix.freeze
+                                                            (?<variant>del|dup|ins)|(?<variant>dup|del|ins)\s?ex\s?(?<exons>\d+)|
+                              (?<variant>dup|del|ins)\s?x\s?(?<exons>\d+(-|_)\d+)/ix.freeze
+
 
           DEPRECATED_BRCA_NAMES_REGEX = /B1|BR1|BRCA\s1|B2|BR2|BRCA\s2/i.freeze
 
@@ -61,6 +64,7 @@ def process_fields(record)
             genotype.add_passthrough_fields(record.mapped_fields,
                                             record.raw_fields,
                                             PASS_THROUGH_FIELDS)
+            
             add_organisationcode_testresult(genotype)
             add_moleculartestingtype(genotype, record)
             process_genetictestcope(genotype, record)
@@ -69,6 +73,7 @@ def process_fields(record)
             @batch.provider = 'RJ7'
             @batch.registryid = 'RJ7'
             res.each { |cur_genotype| @persister.integrate_and_store(cur_genotype) }
+            
           end
 
           def add_organisationcode_testresult(genotype)
@@ -138,8 +143,8 @@ def process_deprecated_gene(deprecated_gene, positive_genes)
           end
 
           def process_fullscreen_records(genotype, record, positive_genes, genotypes)
-            if normal?(record)
-              normal_full_screen(genotype, genotypes)
+            if ucs_variant?(record)
+              process_ucs_variants(genotype, genotypes, positive_genes, record)       
             elsif failed_test?(record)
               failed_full_screen(genotype, genotypes)
             elsif positive_cdna?(record) || positive_exonvariant?(record)
@@ -148,10 +153,53 @@ def process_fullscreen_records(genotype, record, positive_genes, genotypes)
               else
                 single_variant_full_screen(genotype, genotypes, positive_genes, record)
               end
+            elsif normal?(record)
+              normal_full_screen(genotype, genotypes)
+            else
+              unknown_status(genotype, genotypes, positive_genes, record)
             end
             genotypes
           end
 
+          def ucs_variant?(record)
+            record.raw_fields['genotype'].scan(/ucs/i).size.positive?
+          end 
+
+          def process_ucs_variants(genotype, genotypes, positive_genes, record)
+            if ashkenazi?(record) || polish?(record) || full_screen?(record)
+              negative_gene = %w[BRCA1 BRCA2] - positive_genes
+              genotype_dup = genotype.dup
+              genotype_dup.add_gene(negative_gene.join)
+              genotype_dup.add_status(1)
+              genotypes.append(genotype_dup)
+              genotype.add_gene(positive_genes.join)
+              genotype.add_status(10)
+            else
+              process_single_gene(genotype, record)
+              genotype.add_status(10)  
+            end    
+
+            genotypes.append(genotype)
+          end 
+
+          def unknown_status(genotype, genotypes, positive_genes, record)
+            if ashkenazi?(record) || polish?(record) || full_screen?(record)
+              negative_gene = %w[BRCA1 BRCA2] - positive_genes
+              genotype_dup = genotype.dup
+              genotype_dup.add_gene(negative_gene.join)
+              genotype_dup.add_status(1)
+              genotypes.append(genotype_dup)
+              genotype.add_gene(positive_genes.join)
+              genotype.add_status(4)
+            else
+              process_single_gene(genotype, record)
+              genotype.add_gene(positive_genes.join) if !positive_genes.nil?
+              genotype.add_status(4)  
+            end    
+            genotypes.append(genotype)
+          end 
+
+
           def normal_full_screen(genotype, genotypes)
             %w[BRCA1 BRCA2].each do |negative_gene|
               genotype_dup = genotype.dup
@@ -183,12 +231,17 @@ def single_variant_full_screen(genotype, genotypes, positive_genes, record)
           end
 
           def process_targeted_records(positive_genes, genotype, record, genotypes)
-            if normal?(record)
-              process_normal_targeted(genotype, record, genotypes)
+            if ucs_variant?(record)
+              process_ucs_variants(genotype, genotypes, positive_genes, record)
             elsif failed_test?(record)
               process_failed_targeted(genotype, record, genotypes)
             elsif positive_cdna?(record) || positive_exonvariant?(record)
               process_positive_targeted(record, positive_genes, genotype, genotypes)
+            elsif normal?(record)
+              process_normal_targeted(genotype, record, genotypes)
+            else
+              unknown_status(genotype, genotypes, positive_genes, record)
+
             end
             genotypes
           end
@@ -232,6 +285,7 @@ def process_single_gene(genotype, record)
             else
               @logger.debug "FAILED gene parse for: #{record.raw_fields['genotype']}"
             end
+        
           end
           # rubocop:enable  Lint/DuplicateBranch
 
@@ -266,17 +320,48 @@ def add_variants_multiple_results(variants, genotype, genotypes)
           end
 
           def process_multiple_positive_variants(positive_genes, genotype, record, genotypes)
+            
             if positive_genes.flatten.uniq.size > 1
               variants = process_multi_genes_rec(record, positive_genes)
             elsif positive_genes.flatten.uniq.size == 1
               variants = process_uniq_gene_rec(record, positive_genes)
+            elsif positive_genes.empty?
+              process_multi_variants_no_gene(record, genotype, genotypes)
             end
-
             add_variants_multiple_results(variants, genotype, genotypes) unless variants.nil?
 
             genotypes
           end
 
+          def process_multi_variants_no_gene(record, genotype, genotypes)          
+            return if record.raw_fields['genotype'].nil?
+            record.raw_fields['genotype'].scan(DELIMETER_REGEX)
+            unless $LAST_MATCH_INFO.nil?
+              raw_genotypes = record.raw_fields['genotype'].split($LAST_MATCH_INFO[0])
+              variants =[]
+              raw_genotypes.each do |raw_genotype|
+                genotype_dup = genotype.dup
+                mutation = get_cdna_mutation(raw_genotype)
+                protein = get_protein_impact(raw_genotype)
+                genotype_dup.add_gene_location(mutation[0]) unless mutation.nil?
+                genotype_dup.add_protein_impact(protein[0]) unless protein.nil?
+                genotype_dup.add_status(2)
+                genotypes.append(genotype_dup)
+              end
+          end 
+          create_empty_brca_tests(record, genotype, genotypes) if full_screen?(record)          
+        end 
+
+          def create_empty_brca_tests(record, genotype, genotypes)
+            fs_genes = ['BRCA1', 'BRCA2']
+            fs_genes.each do |fs_gene|
+              genotype_dup = genotype.dup
+              genotype_dup.add_gene(fs_gene)
+              genotype_dup.add_status(4)
+              genotypes.append(genotype_dup)
+            end
+          end 
+
           def process_multi_genes_rec(record, positive_genes)
             if record.raw_fields['genotype'].scan(DELIMETER_REGEX).size > 1
               variants = process_single_variant(record, positive_genes)
@@ -431,10 +516,12 @@ def failed_test?(record)
           end
 
           def void_genetictestscope?(record)
-            return if record.raw_fields['moleculartestingtype'].nil?
-
+            return if record.raw_fields['moleculartestingtype'].nil? 
+            
             record.raw_fields['moleculartestingtype'].empty? ||
-              record.raw_fields['moleculartestingtype'] == 'Store'
+            record.raw_fields['moleculartestingtype'] == 'Store' ||
+            record.raw_fields['moleculartestingtype'] == 'Reclassification of previous result'
+
           end
         end
         # rubocop:enable Metrics/ClassLength
diff --git a/test/lib/import/brca/providers/st_george_old/st_george_handler_old_test.rb b/test/lib/import/brca/providers/st_george_old/st_george_handler_old_test.rb
index 9bb67c25..07312bea 100644
--- a/test/lib/import/brca/providers/st_george_old/st_george_handler_old_test.rb
+++ b/test/lib/import/brca/providers/st_george_old/st_george_handler_old_test.rb
@@ -134,6 +134,33 @@ def setup
     assert_equal 'c.6275_6276del', variants[1].attribute_map['codingdnasequencechange']
   end
 
+  # test 'process_multi_variants_no_gene' do
+  #   multiple_variants_no_gene_record = build_raw_record('pseudo_id1' => 'bob')
+  #   multiple_variants_no_gene_record.raw_fields['genotype'] = 'c.666A>G + c.6275_6276del'
+  #   genotypes = []
+  #   variants = @handler.process_multi_variants_no_gene(multiple_variants_no_gene_record, @genotype, genotypes)
+  #   assert_equal 2, variants[0].attribute_map['teststatus']
+  #   assert_equal 2, variants[1].attribute_map['teststatus']
+  #   assert_equal nil, variants[0].attribute_map['gene']
+  #   assert_equal nil, variants[1].attribute_map['gene']
+  #   assert_equal 'c.666A>G', variants[0].attribute_map['codingdnasequencechange']
+  #   assert_equal 'c.6275_6276del', variants[1].attribute_map['codingdnasequencechange']  
+  # end     
+  
+  test 'process_ucs_variants' do
+    ucs_variant_record = build_raw_record('pseudo_id1' => 'bob')
+    ucs_variant_record.raw_fields['genotype'] = 'N + BR1 UCS'
+    positive_genes=['BRCA1', 'BRCA2']
+    genotypes = []
+    variants = @handler.process_ucs_variants(@genotype, genotypes, positive_genes, ucs_variant_record)
+    assert_equal 10, variants[0].attribute_map['teststatus']
+    assert_equal 7, variants[0].attribute_map['gene']
+  end  
+
+  test 'unknown_status' do
+  end
+
+
   test 'process_multiple_cdnavariants_protein_for_same_gene' do
     multiple_cdnavariants_record = build_raw_record('pseudo_id1' => 'bob')
     multiple_cdnavariants_record.raw_fields['genotype'] = 'BR1 c.3005delA, c.3119G>A (p.Ser1040Asn)'