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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5906539copy number variation1nstd209human GRCh38 chr5: 17,508,431-17,622,042 , GRCh37.p13 chr5: 17,508,540-17,622,151 H3P18, TAF11L4, 5 more genes
    nsv5905179copy number variation1nstd209human GRCh38 chr5: 17,512,400-17,669,023 , GRCh37.p13 chr5: 17,512,509-17,669,132 TAF11L5, H3P22, 9 more genes
    nsv5580563copy number variation1nstd207human GRCh38 chr5: 17,501,637-17,608,218 , GRCh37.p13 chr5: 17,501,746-17,608,327 H3P18, TAF11L4, 3 more genes
    nsv5472241copy number variation1nstd206human GRCh38 chr5: 17,466,000-17,525,000 , GRCh37.p13 chr5: 17,466,109-17,525,109 TAF11L1, H3Y2, 6 more genes
    nsv5414943copy number variation1nstd206human GRCh38 chr5: 17,517,000-17,530,300 , GRCh37.p13 chr5: 17,517,109-17,530,409 TAF11L5, TAF11L3, 2 more genes
    nsv5381771copy number variation1nstd102humanPathogenic GRCh37 chr5: 22,149-29,048,823 , GRCh38.p12 chr5: 22,149-29,048,716 OTULINL, AKTIPP2, 317 more genes
    nsv5228961copy number variation1nstd204human GRCh38.p13 chr5: 17,517,601-17,530,500 , GRCh37.p13 chr5: 17,517,710-17,530,609 TAF11L6, TAF11L3, 2 more genes
    nsv4944423copy number variation1nstd200human GRCh38 chr5: 17,505,898-17,618,866 , GRCh37.p13 chr5: 17,506,007-17,618,975 H3P18, TAF11L3, 5 more genes
    nsv4944421copy number variation1nstd200human GRCh38 chr5: 17,494,414-17,600,894 , GRCh37.p13 chr5: 17,494,523-17,601,003 TAF11L3, TAF11L2, 4 more genes
    nsv4930707copy number variation1nstd200human GRCh38 chr5: 17,507,721-17,652,813 , GRCh37.p13 chr5: 17,507,830-17,652,922 H3P18, TAF11L4, 7 more genes
    nsv4930706copy number variation1nstd200human GRCh38 chr5: 17,507,457-17,621,129 , GRCh37.p13 chr5: 17,507,566-17,621,238 H3P18, TAF11L4, 5 more genes
    nsv4930705copy number variation1nstd200human GRCh38 chr5: 17,505,149-17,700,498 , GRCh37.p13 chr5: 17,505,258-17,700,607 TAF11L6, H3P19, 9 more genes
    nsv4930704copy number variation1nstd200human GRCh38 chr5: 17,504,838-17,618,341 , GRCh37.p13 chr5: 17,504,947-17,618,450 H3P18, TAF11L4, 4 more genes
    nsv4930703copy number variation1nstd200human GRCh38 chr5: 17,501,934-17,602,076 , GRCh37.p13 chr5: 17,502,043-17,602,185 TAF11L5, TAF11L3, 3 more genes
    nsv4930696copy number variation1nstd200human GRCh38 chr5: 17,483,873-17,633,584 , GRCh37.p13 chr5: 17,483,982-17,633,693 TAF11L1, TAF11L2, 10 more genes
    nsv4930693copy number variation1nstd200human GRCh38 chr5: 17,469,725-17,625,108 , GRCh37.p13 chr5: 17,469,834-17,625,217 H3P18, H3P19, 10 more genes
    nsv4792904copy number variation1nstd200human GRCh37 chr5: 17,512,513-17,669,133 , GRCh38.p12 chr5: 17,512,404-17,669,024 TAF11L4, H3P20, 9 more genes
    nsv4792903copy number variation1nstd200human GRCh37 chr5: 17,507,830-17,652,922 , GRCh38.p12 chr5: 17,507,721-17,652,813 H3P18, TAF11L4, 7 more genes
    nsv4792902copy number variation1nstd200human GRCh37 chr5: 17,507,134-17,793,022 , GRCh38.p12 chr5: 17,507,025-17,792,913 TAF11L4, H3P20, 10 more genes
    nsv4792901copy number variation1nstd200human GRCh37 chr5: 17,502,043-17,602,185 , GRCh38.p12 chr5: 17,501,934-17,602,076 TAF11L3, TAF11L5, 3 more genes
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