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Items: 1 to 20 of 218

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112733copy number variation1nstd102humanPathogenic GRCh37 chr2: 15,640,273-19,609,496 , GRCh38.p12 chr2: 15,500,149-19,409,735 LOC112267888, LOC105373454, 40 more genes
    nsv5963244insertion1nstd209human GRCh38 chr2: 17,642,309-17,642,309 , GRCh37.p13 chr2: 17,823,576-17,823,576 VSNL1
    nsv5694098mobile element insertion1nstd211human GRCh38 chr2: 17,551,916-17,551,916 , GRCh37.p13 chr2: 17,733,183-17,733,183 VSNL1
    nsv5567474copy number variation1nstd207human GRCh38 chr2: 17,622,519-17,622,575 , GRCh37.p13 chr2: 17,803,786-17,803,842 VSNL1
    nsv5447510copy number variation1nstd206human GRCh38 chr2: 17,616,501-17,616,711 , GRCh37.p13 chr2: 17,797,768-17,797,978 VSNL1
    nsv5439571copy number variation1nstd206human GRCh38 chr2: 17,632,011-17,632,427 , GRCh37.p13 chr2: 17,813,278-17,813,694 VSNL1
    nsv5439385copy number variation1nstd206human GRCh38 chr2: 17,569,037-17,569,202 , GRCh37.p13 chr2: 17,750,304-17,750,469 VSNL1
    nsv5381163copy number variation2nstd102humanUncertain significance GRCh37 chr2: 17,034,358-17,963,206 , GRCh38.p12 chr2: 16,853,091-17,781,939 LOC101928149, RAD51AP2, 10 more genes
    nsv5073319mobile element insertion1nstd203human GRCh38 chr2: 17,633,524-17,633,539 , GRCh37.p13 chr2: 17,814,791-17,814,806 VSNL1
    nsv4904813copy number variation1nstd200human GRCh38 chr2: 17,616,501-17,616,711 , GRCh37.p13 chr2: 17,797,768-17,797,978 VSNL1
    nsv4900439copy number variation1nstd200human GRCh38 chr2: 17,638,558-17,639,821 , GRCh37.p13 chr2: 17,819,825-17,821,088 VSNL1
    nsv4900438copy number variation1nstd200human GRCh38 chr2: 17,637,984-17,648,339 , GRCh37.p13 chr2: 17,819,251-17,829,606 VSNL1
    nsv4900437copy number variation1nstd200human GRCh38 chr2: 17,619,882-17,621,067 , GRCh37.p13 chr2: 17,801,149-17,802,334 VSNL1
    nsv4900436copy number variation1nstd200human GRCh38 chr2: 17,574,431-17,575,996 , GRCh37.p13 chr2: 17,755,698-17,757,263 VSNL1
    nsv4775618copy number variation1nstd200human GRCh37 chr2: 17,819,825-17,821,088 , GRCh38.p12 chr2: 17,638,558-17,639,821 VSNL1
    nsv4595121copy number variation1nstd183human GRCh37 chr2: 17,341,974-18,336,233 , GRCh38.p12 chr2: 17,160,707-18,154,967 KCNS3, LOC105373449, 12 more genes
    nsv4464954mobile element insertion1nstd166human GRCh37.p13 chr2: 17,835,984-17,835,984 , GRCh38.p12 chr2: 17,654,717-17,654,717 VSNL1
    nsv4464692mobile element insertion1nstd166human GRCh37.p13 chr2: 17,817,967-17,817,967 , GRCh38.p12 chr2: 17,636,700-17,636,700 VSNL1
    nsv4451073copy number variation1nstd102humanPathogenic GRCh37 chr2: 12,269,293-18,259,781 , GRCh38.p12 chr2: 12,129,167-18,078,515 LINC00276, TRIB2, 49 more genes
    nsv4451022copy number variation1nstd102humanPathogenic GRCh37 chr2: 15,631,145-21,729,493 , GRCh38.p12 chr2: 15,491,021-21,506,621 RAD51AP2, LOC101928149, 82 more genes
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