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Items: 1 to 20 of 548

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6130734insertion1nstd186human GRCh37 chr12: 109,647,778-109,647,781 , GRCh38.p12 chr12: 109,209,973-109,209,976 ACACB
    nsv5975546insertion1nstd209human GRCh38 chr12: 109,209,974-109,209,974 , GRCh37.p13 chr12: 109,647,779-109,647,779 ACACB
    nsv5967692insertion1nstd209human GRCh38 chr12: 109,210,270-109,210,270 , GRCh37.p13 chr12: 109,648,075-109,648,075 ACACB
    nsv5939462copy number variation1nstd209human GRCh38 chr12: 109,209,871-109,210,404 , GRCh37.p13 chr12: 109,647,676-109,648,209 ACACB
    nsv5939148copy number variation1nstd209human GRCh38 chr12: 109,119,247-109,121,161 , GRCh37.p13 chr12: 109,557,052-109,558,966 ACACB, LOC105369974
    nsv5936420copy number variation1nstd209human GRCh38 chr12: 109,194,510-109,194,609 , GRCh37.p13 chr12: 109,632,315-109,632,414 ACACB
    nsv5855006copy number variation1nstd209human GRCh38 chr12: 109,185,994-109,188,643 , GRCh37.p13 chr12: 109,623,799-109,626,448 ACACB
    nsv5848437copy number variation1nstd209human GRCh38 chr12: 109,119,241-109,121,194 , GRCh37.p13 chr12: 109,557,046-109,558,999 LOC105369974, ACACB
    nsv5729836mobile element insertion1nstd211human GRCh38 chr12: 109,247,913-109,247,913 , GRCh37.p13 chr12: 109,685,718-109,685,718 ACACB
    nsv5728993mobile element insertion2nstd211human GRCh38 chr12: 109,225,306-109,225,306 , GRCh37.p13 chr12: 109,663,111-109,663,111 ACACB
    nsv5723470mobile element insertion1nstd211human GRCh38 chr12: 109,155,467-109,155,467 , GRCh37.p13 chr12: 109,593,272-109,593,272 ACACB
    nsv5661348insertion1nstd207human GRCh38 chr12: 109,210,255-109,210,255 , GRCh37.p13 chr12: 109,648,060-109,648,060 ACACB
    nsv5658327insertion1nstd207human GRCh38 chr12: 109,209,912-109,209,912 , GRCh37.p13 chr12: 109,647,717-109,647,717 ACACB
    nsv5657526insertion1nstd207human GRCh38 chr12: 109,209,974-109,209,974 , GRCh37.p13 chr12: 109,647,779-109,647,779 ACACB
    nsv5654979insertion1nstd207human GRCh38 chr12: 109,209,972-109,209,972 , GRCh37.p13 chr12: 109,647,777-109,647,777 ACACB
    nsv5653004insertion1nstd207human GRCh38 chr12: 109,210,235-109,210,235 , GRCh37.p13 chr12: 109,648,040-109,648,040 ACACB
    nsv5645573insertion1nstd207human GRCh38 chr12: 109,210,036-109,210,036 , GRCh37.p13 chr12: 109,647,841-109,647,841 ACACB
    nsv5602623copy number variation1nstd207human GRCh38 chr12: 109,210,297-109,210,354 , GRCh37.p13 chr12: 109,648,102-109,648,159 ACACB
    nsv5587687copy number variation1nstd207human GRCh38 chr12: 109,194,446-109,194,553 , GRCh37.p13 chr12: 109,632,251-109,632,358 ACACB
    nsv5557611mobile element insertion1nstd206human GRCh38 chr12: 109,225,306-109,225,357 , GRCh37.p13 chr12: 109,663,111-109,663,162 ACACB
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