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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
    nsv7076210inversion1nstd229human GRCh38 chr10: 102,852,468-102,989,635 , GRCh37.p13 chr10: 104,612,225-104,749,392 BORCS7-ASMT, CNNM2, 4 more genes
    nsv7061391inversion1nstd229human GRCh38 chr10: 100,357,388-105,969,995 , GRCh37.p13 chr10: 102,117,145-107,729,753 , CALHM1, 127 more genes
    nsv6896023copy number variation1nstd229human GRCh38 chr10: 102,856,086-102,864,225 , GRCh37.p13 chr10: 104,615,843-104,623,982 BORCS7-ASMT, BORCS7
    nsv6885378copy number variation1nstd229human GRCh38 chr10: 102,850,950-102,854,054 , GRCh37.p13 chr10: 104,610,707-104,613,811 BORCS7-ASMT, BORCS7
    nsv6880173copy number variation1nstd229human GRCh38 chr10: 102,843,001-102,876,000 , GRCh37.p13 chr10: 104,602,758-104,635,757 AS3MT, BORCS7, 3 more genes
    nsv6879144copy number variation1nstd229human GRCh38 chr10: 102,859,526-102,859,887 , GRCh37.p13 chr10: 104,619,283-104,619,644 BORCS7, BORCS7-ASMT
    nsv6595323inversion1nstd223human GRCh38 chr10: 102,852,091-102,852,614 , GRCh37.p13 chr10: 104,611,848-104,612,371 BORCS7, BORCS7-ASMT
    nsv6589507inversion1nstd223human GRCh38 chr10: 102,858,059-102,859,171 , GRCh37.p13 chr10: 104,617,816-104,618,928 BORCS7-ASMT, BORCS7
    nsv6587001inversion1nstd223human GRCh38 chr10: 102,854,879-102,855,109 , GRCh37.p13 chr10: 104,614,636-104,614,866 BORCS7-ASMT, BORCS7
    nsv6449998copy number variation1nstd223human GRCh38 chr10: 102,855,159-102,861,970 , GRCh37.p13 chr10: 104,614,916-104,621,727 BORCS7, BORCS7-ASMT
    nsv6247449mobile element insertion1nstd215human GRCh38 chr10: 102,856,240-102,856,240 , GRCh37.p13 chr10: 104,615,997-104,615,997 BORCS7, BORCS7-ASMT
    nsv6131926copy number variation1nstd213human GRCh37 chr10: 103,560,000-105,280,001 , GRCh38.p12 chr10: 101,800,243-103,520,244 ARL3, CYP17A1, 56 more genes
    nsv5910104copy number variation1nstd209human GRCh38 chr10: 102,852,051-102,871,611 , GRCh37.p13 chr10: 104,611,808-104,631,368 AS3MT, BORCS7, 1 more genes
    nsv5856842copy number variation1nstd209human GRCh38 chr10: 102,863,977-102,865,984 , GRCh37.p13 chr10: 104,623,734-104,625,741 BORCS7-ASMT, BORCS7
    nsv5848261copy number variation1nstd209human GRCh38 chr10: 102,855,181-102,871,240 , GRCh37.p13 chr10: 104,614,938-104,630,997 BORCS7-ASMT, BORCS7, 1 more genes
    nsv5549767insertion1nstd206human GRCh38 chr10: 102,853,728-102,853,739 , GRCh37.p13 chr10: 104,613,485-104,613,496 BORCS7-ASMT, BORCS7
    nsv5354434translocation1nstd200human GRCh38 chr10: 102,854,265-102,854,265 , GRCh38 chrX: 117,399,380-117,399,380 , GRCh37.p13 chr10: 104,614,022-104,614,022 , GRCh37.p13 chrX: 116,533,343-116,533,343 BORCS7, TCERG1P1, 1 more genes
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