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Items: 1 to 20 of 473

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5969289inversion1nstd209human GRCh38 chr2: 10,686,898-10,687,878 , GRCh37.p13 chr2: 10,827,024-10,828,004 NOL10
    nsv5965858insertion1nstd209human GRCh38 chr2: 10,690,415-10,690,415 , GRCh37.p13 chr2: 10,830,541-10,830,541 NOL10, RN7SL832P
    nsv5963737insertion1nstd209human GRCh38 chr2: 10,595,136-10,595,136 , GRCh37.p13 chr2: 10,735,262-10,735,262 NOL10
    nsv5960394insertion1nstd209human GRCh38 chr2: 10,675,901-10,675,901 , GRCh37.p13 chr2: 10,816,027-10,816,027 NOL10
    nsv5958151insertion1nstd209human GRCh38 chr2: 10,587,023-10,587,023 , GRCh37.p13 chr2: 10,727,149-10,727,149 NOL10
    nsv5879994copy number variation1nstd209human GRCh38 chr2: 10,679,102-10,680,016 , GRCh37.p13 chr2: 10,819,228-10,820,142 NOL10
    nsv5870781copy number variation1nstd209human GRCh38 chr2: 10,587,067-10,587,260 , GRCh37.p13 chr2: 10,727,193-10,727,386 NOL10
    nsv5870420copy number variation1nstd209human GRCh38 chr2: 10,634,956-10,636,746 , GRCh37.p13 chr2: 10,775,082-10,776,872 NOL10
    nsv5830884copy number variation1nstd209human GRCh38 chr2: 10,634,898-10,636,197 , GRCh37.p13 chr2: 10,775,024-10,776,323 NOL10
    nsv5685948mobile element insertion1nstd211human GRCh38 chr2: 10,600,670-10,600,670 , GRCh37.p13 chr2: 10,740,796-10,740,796 NOL10
    nsv5678551mobile element insertion1nstd211human GRCh38 chr2: 10,581,337-10,581,337 , GRCh37.p13 chr2: 10,721,463-10,721,463 NOL10
    nsv5617478insertion1nstd207human GRCh38 chr2: 10,685,912-10,685,912 , GRCh37.p13 chr2: 10,826,038-10,826,038 NOL10
    nsv5612690insertion1nstd207human GRCh38 chr2: 10,587,088-10,587,088 , GRCh37.p13 chr2: 10,727,214-10,727,214 NOL10
    nsv5566943copy number variation1nstd207human GRCh38 chr2: 10,587,072-10,587,259 , GRCh37.p13 chr2: 10,727,198-10,727,385 NOL10
    nsv5546997insertion1nstd206human GRCh38 chr2: 10,685,912-10,685,912 , GRCh37.p13 chr2: 10,826,038-10,826,038 NOL10
    nsv5453289copy number variation1nstd206human GRCh38 chr2: 10,639,157-10,640,097 , GRCh37.p13 chr2: 10,779,283-10,780,223 NOL10
    nsv5446543copy number variation1nstd206human GRCh38 chr2: 10,634,961-10,636,747 , GRCh37.p13 chr2: 10,775,087-10,776,873 NOL10
    nsv5443149copy number variation1nstd206human GRCh38 chr2: 10,654,398-10,654,478 , GRCh37.p13 chr2: 10,794,524-10,794,604 NOL10
    nsv5438092copy number variation1nstd206human GRCh38 chr2: 10,650,278-10,650,458 , GRCh37.p13 chr2: 10,790,404-10,790,584 NOL10
    nsv5409278mobile element insertion1nstd206human GRCh38 chr2: 10,600,670-10,600,721 , GRCh37.p13 chr2: 10,740,796-10,740,847 NOL10
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