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Items: 1 to 20 of 1414

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5967308insertion1nstd209human GRCh38 chr8: 51,790,811-51,790,811 , GRCh37.p13 chr8: 52,703,371-52,703,371 PXDNL
    nsv5956639insertion1nstd209human GRCh38 chr8: 51,696,870-51,696,870 , GRCh37.p13 chr8: 52,609,430-52,609,430 PXDNL
    nsv5949274insertion1nstd209human GRCh38 chr8: 51,428,965-51,428,965 , GRCh37.p13 chr8: 52,341,525-52,341,525 PXDNL
    nsv5926460copy number variation1nstd209human GRCh38 chr8: 51,743,582-51,746,922 , GRCh37.p13 chr8: 52,656,142-52,659,482 PXDNL
    nsv5922656copy number variation1nstd209human GRCh38 chr8: 51,533,462-51,535,742 , GRCh37.p13 chr8: 52,446,022-52,448,302 PXDNL
    nsv5921088copy number variation1nstd209human GRCh38 chr8: 51,761,542-51,762,712 , GRCh37.p13 chr8: 52,674,102-52,675,272 PXDNL, LOC105375833
    nsv5921007copy number variation1nstd209human GRCh38 chr8: 51,607,616-51,608,612 , GRCh37.p13 chr8: 52,520,176-52,521,172 PXDNL
    nsv5917816copy number variation1nstd209human GRCh38 chr8: 51,347,686-51,347,771 , GRCh37.p13 chr8: 52,260,246-52,260,331 PXDNL
    nsv5915696copy number variation1nstd209human GRCh38 chr8: 51,538,754-51,582,010 , GRCh37.p13 chr8: 52,451,314-52,494,570 PXDNL
    nsv5914220copy number variation1nstd209human GRCh38 chr8: 51,657,445-51,658,905 , GRCh37.p13 chr8: 52,570,005-52,571,465 PXDNL
    nsv5911805copy number variation1nstd209human GRCh38 chr8: 51,682,885-51,685,184 , GRCh37.p13 chr8: 52,595,445-52,597,744 PXDNL
    nsv5911210copy number variation1nstd209human GRCh38 chr8: 51,727,736-51,727,786 , GRCh37.p13 chr8: 52,640,296-52,640,346 PXDNL
    nsv5910585copy number variation1nstd209human GRCh38 chr8: 51,404,349-51,404,586 , GRCh37.p13 chr8: 52,316,909-52,317,146 PXDNL
    nsv5910507copy number variation1nstd209human GRCh38 chr8: 51,533,992-51,534,071 , GRCh37.p13 chr8: 52,446,552-52,446,631 PXDNL
    nsv5910372copy number variation1nstd209human GRCh38 chr8: 51,321,602-51,321,679 , GRCh37.p13 chr8: 52,234,162-52,234,239 PXDNL
    nsv5909632copy number variation1nstd209human GRCh38 chr8: 51,454,942-51,455,130 , GRCh37.p13 chr8: 52,367,502-52,367,690 PXDNL
    nsv5909266copy number variation1nstd209human GRCh38 chr8: 51,378,682-51,378,793 , GRCh37.p13 chr8: 52,291,242-52,291,353 PXDNL
    nsv5867049copy number variation1nstd209human GRCh38 chr8: 51,538,921-51,580,742 , GRCh37.p13 chr8: 52,451,481-52,493,302 PXDNL
    nsv5864388copy number variation2nstd209human GRCh38 chr8: 51,745,043-51,747,042 , GRCh37.p13 chr8: 52,657,603-52,659,602 PXDNL
    nsv5864381copy number variation1nstd209human GRCh38 chr8: 51,683,626-51,684,825 , GRCh37.p13 chr8: 52,596,186-52,597,385 PXDNL
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