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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112738copy number variation1nstd102humanPathogenic GRCh37 chr6: 149,619-3,951,208 , GRCh38.p12 chr6: 149,619-3,950,974 LINC01600, TUBB2BP1, 66 more genes
    nsv5952576insertion1nstd209human GRCh38 chr6: 3,362,416-3,362,416 , GRCh37.p13 chr6: 3,362,650-3,362,650 SLC22A23
    nsv5906450copy number variation1nstd209human GRCh38 chr6: 3,331,352-3,336,079 , GRCh37.p13 chr6: 3,331,586-3,336,313 SLC22A23
    nsv5901351copy number variation1nstd209human GRCh38 chr6: 3,366,253-3,366,326 , GRCh37.p13 chr6: 3,366,487-3,366,560 SLC22A23
    nsv5898364copy number variation1nstd209human GRCh38 chr6: 3,365,252-3,366,271 , GRCh37.p13 chr6: 3,365,486-3,366,505 SLC22A23
    nsv5896772copy number variation1nstd209human GRCh38 chr6: 3,441,831-3,446,541 , GRCh37.p13 chr6: 3,442,065-3,446,775 SLC22A23
    nsv5891637copy number variation1nstd209human GRCh38 chr6: 3,402,428-3,402,560 , GRCh37.p13 chr6: 3,402,662-3,402,794 SLC22A23
    nsv5888356copy number variation1nstd209human GRCh38 chr6: 3,326,969-3,327,040 , GRCh37.p13 chr6: 3,327,203-3,327,274 SLC22A23
    nsv5845250copy number variation1nstd209human GRCh38 chr6: 3,442,311-3,446,610 , GRCh37.p13 chr6: 3,442,545-3,446,844 SLC22A23
    nsv5845149copy number variation1nstd209human GRCh38 chr6: 3,365,122-3,366,321 , GRCh37.p13 chr6: 3,365,356-3,366,555 SLC22A23
    nsv5844940copy number variation1nstd209human GRCh38 chr6: 3,331,345-3,336,104 , GRCh37.p13 chr6: 3,331,579-3,336,338 SLC22A23
    nsv5725712mobile element insertion1nstd211human GRCh38 chr6: 3,385,818-3,385,818 , GRCh37.p13 chr6: 3,386,052-3,386,052 SLC22A23
    nsv5682472mobile element insertion2nstd211human GRCh38 chr6: 3,355,949-3,355,949 , GRCh37.p13 chr6: 3,356,183-3,356,183 SLC22A23
    nsv5633540insertion2nstd207human GRCh38 chr6: 3,356,090-3,356,090 , GRCh37.p13 chr6: 3,356,324-3,356,324 SLC22A23
    nsv5631504insertion1nstd207human GRCh38 chr6: 3,310,416-3,310,416 , GRCh37.p13 chr6: 3,310,650-3,310,650 SLC22A23
    nsv5630921insertion2nstd207human GRCh38 chr6: 3,402,417-3,402,417 , GRCh37.p13 chr6: 3,402,651-3,402,651 SLC22A23
    nsv5565648copy number variation1nstd207human GRCh38 chr6: 3,310,321-3,310,379 , GRCh37.p13 chr6: 3,310,555-3,310,613 SLC22A23
    nsv5560290sequence alteration1nstd206human GRCh38 chr6: 3,280,492-3,281,158 , GRCh37.p13 chr6: 3,280,726-3,281,392 SLC22A23, PSMG4
    nsv5553631insertion1nstd206human GRCh38 chr6: 3,439,118-3,439,120 , GRCh37.p13 chr6: 3,439,352-3,439,354 SLC22A23
    nsv5548586insertion1nstd206human GRCh38 chr6: 3,402,455-3,402,468 , GRCh37.p13 chr6: 3,402,689-3,402,702 SLC22A23
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