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Items: 1 to 20 of 215

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137211copy number variation1nstd102humanPathogenic GRCh37 chr10: 11,138,692-135,427,143 , GRCh38.p12 chr10: 11,096,729-133,613,639 EXOC6, VCL, 1906 more genes
    nsv7137209copy number variation1nstd102humanPathogenic GRCh37 chr10: 12,829,206-135,427,143 , GRCh38.p12 chr10: 12,787,207-133,613,639 RNU7-12P, RNU1-65P, 1876 more genes
    nsv7093788copy number variation1nstd102humanUncertain significance GRCh37 chr10: 30,602,538-31,816,192 , GRCh38.p12 chr10: 30,313,609-31,527,264 LOC100505502, HNRNPA1P32, 24 more genes
    nsv7070202inversion1nstd229human GRCh38 chr10: 27,330,033-30,802,827 , GRCh37.p13 chr10: 27,618,962-31,091,756 LINC00837, RPL21P93, 77 more genes
    nsv7058187inversion1nstd229human GRCh38 chr10: 27,002,297-30,809,591 , GRCh37.p13 chr10: 27,291,226-31,098,520 RNU6-490P, LOC105376474, 87 more genes
    nsv6894377copy number variation1nstd229human GRCh38 chr10: 28,466,728-36,061,502 , GRCh37.p13 chr10: 28,755,657-36,350,430 LOC105376482, LOC101929431, 130 more genes
    nsv6894268copy number variation1nstd229human GRCh38 chr10: 30,707,981-30,712,344 , GRCh37.p13 chr10: 30,996,910-31,001,273 SVIL2P
    nsv6882223copy number variation1nstd229human GRCh38 chr10: 30,705,654-30,705,758 , GRCh37.p13 chr10: 30,994,583-30,994,687 SVIL2P
    nsv6881880copy number variation1nstd229human GRCh38 chr10: 30,621,541-30,866,519 , GRCh37.p13 chr10: 30,910,470-31,155,448 SVIL2P, LYZL2, 2 more genes
    nsv6585948inversion1nstd223human GRCh38 chr10: 29,962,200-31,017,471 , GRCh37.p13 chr10: 30,251,129-31,306,400 LYZL2, MIR7162, 22 more genes
    nsv6582027inversion1nstd223human GRCh38 chr10: 26,903,422-36,846,484 , GRCh37.p13 chr10: 27,192,351-37,135,412 KIF5B, EPC1-AS1, 167 more genes
    nsv6444594copy number variation1nstd223human GRCh38 chr10: 30,621,541-30,866,516 , GRCh37.p13 chr10: 30,910,470-31,155,445 LINC02644, SVIL2P, 2 more genes
    nsv6443039copy number variation1nstd223human GRCh38 chr10: 30,695,901-30,698,000 , GRCh37.p13 chr10: 30,984,830-30,986,929 SVIL2P
    nsv6442247copy number variation1nstd223human GRCh38 chr10: 30,689,482-30,694,142 , GRCh37.p13 chr10: 30,978,411-30,983,071 SVIL2P
    nsv6437250copy number variation1nstd223human GRCh38 chr10: 30,706,879-30,721,499 , GRCh37.p13 chr10: 30,995,808-31,010,428 LINC02644, SVIL2P
    nsv6313952copy number variation1nstd102humanPathogenic GRCh37 chr10: 6,273,934-34,732,521 , GRCh38.p12 chr10: 6,231,971-34,443,593 RPL36AP55, HNRNPA1P32, 418 more genes
    nsv6290893copy number variation1nstd102humannot provided GRCh37 chr10: 135,655-47,688,677 , GRCh38.p12 chr10: 89,715-47,923,579 C1QL3, LOC105376441, 774 more genes
    nsv6290264copy number variation1nstd102humanPathogenic GRCh37 chr10: 30,624,523-33,688,350 , GRCh38.p12 chr10: 30,335,594-33,399,422 PPIAP31, RNU6-1244P, 54 more genes
    nsv6240537mobile element insertion1nstd215human GRCh38 chr10: 30,712,350-30,712,350 , GRCh37.p13 chr10: 31,001,279-31,001,279 SVIL2P
    nsv6177333copy number variation1nstd214human GRCh38 chr10: 30,705,653-30,705,755 , GRCh37.p13 chr10: 30,994,582-30,994,684 SVIL2P
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