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Items: 1 to 20 of 387

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6129211insertion1nstd186human GRCh37 chr12: 122,319,733-122,319,763 , GRCh38.p12 chr12: 121,881,827-121,881,857 HPD
    nsv6120695copy number variation1nstd186human GRCh37 chr12: 122,282,572-122,283,380 , GRCh38.p12 chr12: 121,844,666-121,845,474 HPD
    nsv5978803insertion1nstd209human GRCh38 chr12: 121,881,827-121,881,827 , GRCh37.p13 chr12: 122,319,733-122,319,733 HPD
    nsv5973346inversion1nstd209human GRCh38 chr12: 118,054,601-123,705,841 , GRCh37.p13 chr12: 118,492,406-124,190,388 , ACADS, 162 more genes
    nsv5934754copy number variation1nstd209human GRCh38 chr12: 121,844,941-121,845,558 , GRCh37.p13 chr12: 122,282,847-122,283,464 HPD
    nsv5933621copy number variation1nstd209human GRCh38 chr12: 121,844,957-121,845,473 , GRCh37.p13 chr12: 122,282,863-122,283,379 HPD
    nsv5928118copy number variation1nstd209human GRCh38 chr12: 121,851,677-121,852,021 , GRCh37.p13 chr12: 122,289,583-122,289,927 HPD
    nsv5861079copy number variation1nstd209human GRCh38 chr12: 121,866,448-121,868,047 , GRCh37.p13 chr12: 122,304,354-122,305,953 HPD, TIALD
    nsv5849651copy number variation1nstd209human GRCh38 chr12: 121,837,570-121,840,121 , GRCh37.p13 chr12: 122,275,476-122,278,027 HPD
    nsv5695329mobile element insertion2nstd211human GRCh38 chr12: 121,861,568-121,861,568 , GRCh37.p13 chr12: 122,299,474-122,299,474 TIALD, HPD
    nsv5650625insertion1nstd207human GRCh38 chr12: 121,881,808-121,881,808 , GRCh37.p13 chr12: 122,319,714-122,319,714 HPD
    nsv5589484copy number variation1nstd207human GRCh38 chr12: 121,844,957-121,845,473 , GRCh37.p13 chr12: 122,282,863-122,283,379 HPD
    nsv5585484copy number variation1nstd207human GRCh38 chr12: 121,851,677-121,852,021 , GRCh37.p13 chr12: 122,289,583-122,289,927 HPD
    nsv5550370insertion1nstd206human GRCh38 chr12: 121,881,827-121,881,857 , GRCh37.p13 chr12: 122,319,733-122,319,763 HPD
    nsv5510484copy number variation1nstd206human GRCh38 chr12: 121,885,886-121,885,976 , GRCh37.p13 chr12: 122,323,792-122,323,882 HPD
    nsv5509237copy number variation1nstd206human GRCh38 chr12: 121,884,730-121,884,801 , GRCh37.p13 chr12: 122,322,636-122,322,707 HPD
    nsv5502262copy number variation1nstd206human GRCh38 chr12: 121,869,602-121,870,738 , GRCh37.p13 chr12: 122,307,508-122,308,644 HPD, TIALD
    nsv5500537copy number variation1nstd206human GRCh38 chr12: 121,844,666-121,845,474 , GRCh37.p13 chr12: 122,282,572-122,283,380 HPD
    nsv5498867copy number variation1nstd206human GRCh38 chr12: 121,851,690-121,852,022 , GRCh37.p13 chr12: 122,289,596-122,289,928 HPD
    nsv5498587copy number variation1nstd206human GRCh38 chr12: 121,841,429-121,843,235 , GRCh37.p13 chr12: 122,279,335-122,281,141 HPD
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