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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6916859copy number variation1nstd229human GRCh38 chr11: 75,727,030-75,727,189 , GRCh37.p13 chr11: 75,438,075-75,438,234 MOGAT2
    nsv6911698copy number variation1nstd229human GRCh38 chr11: 75,730,262-75,733,548 , GRCh37.p13 chr11: 75,441,307-75,444,593 MOGAT2
    nsv6899215copy number variation1nstd229human GRCh38 chr11: 75,042,869-75,776,821 , GRCh37.p13 chr11: 74,753,914-75,487,866 DGAT2, LOC100421207, 25 more genes
    nsv6595489inversion1nstd223human GRCh38 chr11: 75,730,034-75,730,635 , GRCh37.p13 chr11: 75,441,079-75,441,680 MOGAT2
    nsv6594839inversion1nstd223human GRCh38 chr11: 75,729,743-75,730,913 , GRCh37.p13 chr11: 75,440,788-75,441,958 MOGAT2
    nsv6465320copy number variation1nstd223human GRCh38 chr11: 75,721,477-75,722,044 , GRCh37.p13 chr11: 75,432,522-75,433,089 MOGAT2
    nsv6315537copy number variation1nstd102humanPathogenic GRCh37 chr11: 32,799,481-134,938,470 , GRCh38.p12 chr11: 32,777,935-135,068,576 PYGM, ATL3, 2125 more genes
    nsv6132278copy number variation1nstd213human GRCh37 chr11: 75,150,000-75,550,001 , GRCh38.p12 chr11: 75,438,955-75,838,956 MAP6, DGAT2, 11 more genes
    nsv6081701insertion1nstd212human GRCh38 chr11: 75,731,453-75,731,453 , GRCh37.p13 chr11: 75,442,498-75,442,498 MOGAT2
    nsv5967974insertion1nstd209human GRCh38 chr11: 75,731,453-75,731,453 , GRCh37.p13 chr11: 75,442,498-75,442,498 MOGAT2
    nsv5657988insertion1nstd207human GRCh38 chr11: 75,727,030-75,727,030 , GRCh37.p13 chr11: 75,438,075-75,438,075 MOGAT2
    nsv5645492insertion1nstd207human GRCh38 chr11: 75,731,453-75,731,453 , GRCh37.p13 chr11: 75,442,498-75,442,498 MOGAT2
    nsv5513125copy number variation1nstd206human GRCh38 chr11: 75,727,030-75,727,189 , GRCh37.p13 chr11: 75,438,075-75,438,234 MOGAT2
    nsv5412969mobile element insertion1nstd206human GRCh38 chr11: 75,731,453-75,731,453 , GRCh37.p13 chr11: 75,442,498-75,442,498 MOGAT2
    nsv5380796copy number variation1nstd102humanPathogenic GRCh37 chr11: 11,835,569-118,373,112 , GRCh38.p12 chr11: 11,814,022-118,502,397 FAUP4, MMP7, 2031 more genes
    nsv5302298copy number variation1nstd204human GRCh38.p13 chr11: 75,727,024-75,727,194 , GRCh37.p13 chr11: 75,438,069-75,438,239 MOGAT2
    nsv5136732mobile element insertion1nstd203human GRCh38 chr11: 75,715,886-75,715,901 , GRCh37.p13 chr11: 75,426,931-75,426,946 LOC105369392, MOGAT2
    nsv4985147copy number variation1nstd200human GRCh38 chr11: 75,727,030-75,727,189 , GRCh37.p13 chr11: 75,438,075-75,438,234 MOGAT2
    nsv4838486copy number variation1nstd200human GRCh37 chr11: 75,438,075-75,438,234 , GRCh38.p12 chr11: 75,727,030-75,727,189 MOGAT2
    nsv4768457insertion1nstd186human GRCh37 chr11: 75,442,494-75,442,494 , GRCh38.p12 chr11: 75,731,449-75,731,449 MOGAT2
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