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Items: 1 to 20 of 779

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5965209insertion1nstd209human GRCh38 chr3: 10,365,830-10,365,830 , GRCh37.p13 chr3: 10,407,514-10,407,514 ATP2B2
    nsv5958752insertion1nstd209human GRCh38 chr3: 10,578,380-10,578,380 , GRCh37.p13 chr3: 10,620,064-10,620,064 ATP2B2
    nsv5957280insertion1nstd209human GRCh38 chr3: 10,469,024-10,469,024 , GRCh37.p13 chr3: 10,510,708-10,510,708 ATP2B2
    nsv5904127copy number variation1nstd209human GRCh38 chr3: 9,996,659-11,875,087 , GRCh37.p13 chr3: 10,038,343-11,916,561 , EMC3, 35 more genes
    nsv5904074copy number variation1nstd209human GRCh38 chr3: 10,430,473-10,430,550 , GRCh37.p13 chr3: 10,472,157-10,472,234 ATP2B2
    nsv5901554copy number variation1nstd209human GRCh38 chr3: 10,445,317-10,445,379 , GRCh37.p13 chr3: 10,487,001-10,487,063 ATP2B2
    nsv5901270copy number variation1nstd209human GRCh38 chr3: 10,048,544-11,870,471 , GRCh37.p13 chr3: 10,090,228-11,911,945 , SLC6A11, 29 more genes
    nsv5900669copy number variation1nstd209human GRCh38 chr3: 10,507,910-10,507,960 , GRCh37.p13 chr3: 10,549,594-10,549,644 ATP2B2
    nsv5899041copy number variation1nstd209human GRCh38 chr3: 10,564,504-10,564,670 , GRCh37.p13 chr3: 10,606,188-10,606,354 ATP2B2
    nsv5891525copy number variation1nstd209human GRCh38 chr3: 9,996,478-11,874,953 , GRCh37.p13 chr3: 10,038,162-11,916,427 , TATDN2, 35 more genes
    nsv5891210copy number variation1nstd209human GRCh38 chr3: 10,355,791-10,356,147 , GRCh37.p13 chr3: 10,397,475-10,397,831 ATP2B2
    nsv5730557mobile element insertion1nstd211human GRCh38 chr3: 10,440,769-10,440,769 , GRCh37.p13 chr3: 10,482,453-10,482,453 ATP2B2
    nsv5723211mobile element insertion1nstd211human GRCh38 chr3: 10,594,733-10,594,733 , GRCh37.p13 chr3: 10,636,418-10,636,418 ATP2B2
    nsv5719093mobile element insertion1nstd211human GRCh38 chr3: 10,360,360-10,360,360 , GRCh37.p13 chr3: 10,402,044-10,402,044 ATP2B2
    nsv5693624mobile element insertion1nstd211human GRCh38 chr3: 10,609,569-10,609,569 , GRCh37.p13 chr3: 10,651,254-10,651,254 ATP2B2
    nsv5691857mobile element insertion2nstd211human GRCh38 chr3: 10,469,040-10,469,040 , GRCh37.p13 chr3: 10,510,724-10,510,724 ATP2B2
    nsv5690629mobile element insertion1nstd211human GRCh38 chr3: 10,543,637-10,543,637 , GRCh37.p13 chr3: 10,585,321-10,585,321 ATP2B2
    nsv5685802mobile element insertion1nstd211human GRCh38 chr3: 10,631,766-10,631,766 , GRCh37.p13 chr3: 10,673,451-10,673,451 ATP2B2
    nsv5681227mobile element insertion2nstd211human GRCh38 chr3: 10,584,102-10,584,102 , GRCh37.p13 chr3: 10,625,786-10,625,786 ATP2B2
    nsv5622156insertion1nstd207human GRCh38 chr3: 10,365,830-10,365,830 , GRCh37.p13 chr3: 10,407,514-10,407,514 ATP2B2
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