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Items: 1 to 20 of 331

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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
    nsv7093904copy number variation1nstd102humanUncertain significance GRCh37 chr10: 99,344,461-105,992,004 , GRCh38.p12 chr10: 97,584,704-104,232,246 ABCC2, LBX1-AS1, 160 more genes
    nsv7072186inversion1nstd229human GRCh38 chr10: 102,804,870-102,805,035 , GRCh37.p13 chr10: 104,564,627-104,564,792 WBP1L
    nsv7061391inversion1nstd229human GRCh38 chr10: 100,357,388-105,969,995 , GRCh37.p13 chr10: 102,117,145-107,729,753 , CALHM1, 127 more genes
    nsv6897495copy number variation1nstd229human GRCh38 chr10: 102,772,526-102,772,835 , GRCh37.p13 chr10: 104,532,283-104,532,592 WBP1L
    nsv6896510copy number variation1nstd229human GRCh38 chr10: 102,784,222-102,787,759 , GRCh37.p13 chr10: 104,543,979-104,547,516 WBP1L
    nsv6894178copy number variation1nstd229human GRCh38 chr10: 102,788,353-102,791,542 , GRCh37.p13 chr10: 104,548,110-104,551,299 WBP1L
    nsv6889952copy number variation1nstd229human GRCh38 chr10: 102,770,280-102,770,319 , GRCh37.p13 chr10: 104,530,037-104,530,076 WBP1L
    nsv6886483copy number variation1nstd229human GRCh38 chr10: 102,785,126-102,785,481 , GRCh37.p13 chr10: 104,544,883-104,545,238 WBP1L
    nsv6886072copy number variation1nstd229human GRCh38 chr10: 102,809,113-102,809,408 , GRCh37.p13 chr10: 104,568,870-104,569,165 WBP1L
    nsv6884486copy number variation1nstd229human GRCh38 chr10: 102,799,524-102,805,155 , GRCh37.p13 chr10: 104,559,281-104,564,912 WBP1L, RNU6-1231P
    nsv6884470copy number variation1nstd229human GRCh38 chr10: 102,753,683-102,757,702 , GRCh37.p13 chr10: 104,513,440-104,517,459 WBP1L
    nsv6881390copy number variation1nstd229human GRCh38 chr10: 102,768,365-102,768,690 , GRCh37.p13 chr10: 104,528,122-104,528,447 WBP1L
    nsv6880675copy number variation1nstd229human GRCh38 chr10: 102,758,880-102,763,180 , GRCh37.p13 chr10: 104,518,637-104,522,937 WBP1L
    nsv6880433copy number variation1nstd229human GRCh38 chr10: 102,804,498-102,807,269 , GRCh37.p13 chr10: 104,564,255-104,567,026 RNU6-1231P, WBP1L
    nsv6880405copy number variation1nstd229human GRCh38 chr10: 102,746,601-102,748,800 , GRCh37.p13 chr10: 104,506,358-104,508,557 WBP1L
    nsv6583564inversion1nstd223human GRCh38 chr10: 102,771,594-102,771,983 , GRCh37.p13 chr10: 104,531,351-104,531,740 WBP1L
    nsv6578014inversion1nstd223human GRCh38 chr10: 102,747,164-102,747,834 , GRCh37.p13 chr10: 104,506,921-104,507,591 WBP1L
    nsv6575727inversion1nstd223human GRCh38 chr10: 102,803,623-102,804,388 , GRCh37.p13 chr10: 104,563,380-104,564,145 RNU6-1231P, WBP1L
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