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Items: 1 to 20 of 328

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6113346mobile element insertion1nstd186human GRCh37 chr20: 13,704,145-13,704,145 , GRCh38.p12 chr20: 13,723,498-13,723,498 ESF1
    nsv5978242insertion1nstd209human GRCh38 chr20: 13,733,099-13,733,099 , GRCh37.p13 chr20: 13,713,746-13,713,746 ESF1
    nsv5947235copy number variation1nstd209human GRCh38 chr20: 13,747,831-13,752,096 , GRCh37.p13 chr20: 13,728,478-13,732,743 ESF1
    nsv5932217copy number variation1nstd209human GRCh38 chr20: 13,748,497-13,748,560 , GRCh37.p13 chr20: 13,729,144-13,729,207 ESF1
    nsv5927956copy number variation1nstd209human GRCh38 chr20: 13,734,004-13,736,415 , GRCh37.p13 chr20: 13,714,651-13,717,062 ESF1
    nsv5868224copy number variation1nstd209human GRCh38 chr20: 13,748,662-13,751,987 , GRCh37.p13 chr20: 13,729,309-13,732,634 ESF1
    nsv5703329mobile element insertion2nstd211human GRCh38 chr20: 13,723,514-13,723,514 , GRCh37.p13 chr20: 13,704,161-13,704,161 ESF1
    nsv5671669insertion1nstd207human GRCh38 chr20: 13,723,498-13,723,498 , GRCh37.p13 chr20: 13,704,145-13,704,145 ESF1
    nsv5670786insertion1nstd207human GRCh38 chr20: 13,733,099-13,733,099 , GRCh37.p13 chr20: 13,713,746-13,713,746 ESF1
    nsv5559387sequence alteration1nstd206human GRCh38 chr20: 13,719,198-13,719,198 , GRCh37.p13 chr20: 13,699,845-13,699,845 ESF1
    nsv5539410insertion1nstd206human GRCh38 chr20: 13,733,105-13,733,115 , GRCh37.p13 chr20: 13,713,752-13,713,762 ESF1
    nsv5537659insertion1nstd206human GRCh38 chr20: 13,719,189-13,719,189 , GRCh37.p13 chr20: 13,699,836-13,699,836 ESF1
    nsv5532159copy number variation1nstd206human GRCh38 chr20: 13,764,425-13,764,489 , GRCh37.p13 chr20: 13,745,072-13,745,136 ESF1
    nsv5531306copy number variation1nstd206human GRCh38 chr20: 13,566,939-13,768,096 , GRCh37.p13 chr20: 13,547,586-13,748,743 TASP1, ESF1
    nsv5525492copy number variation1nstd206human GRCh38 chr20: 13,733,807-13,733,859 , GRCh37.p13 chr20: 13,714,454-13,714,506 ESF1
    nsv5524936copy number variation1nstd206human GRCh38 chr20: 13,784,358-13,784,536 , GRCh37.p13 chr20: 13,765,004-13,765,182 NDUFAF5, ESF1
    nsv5515304copy number variation1nstd206human GRCh38 chr20: 13,774,522-13,774,614 , GRCh37.p13 chr20: 13,755,168-13,755,260 ESF1
    nsv5422658mobile element insertion1nstd206human GRCh38 chr20: 13,723,498-13,723,498 , GRCh37.p13 chr20: 13,704,145-13,704,145 ESF1
    nsv5350145translocation1nstd200human GRCh38 chr20: 13,764,489-13,764,489 , GRCh38 chr20: 13,764,425-13,764,425 , GRCh37.p13 chr20: 13,745,072-13,745,072 , GRCh37.p13 chr20: 13,745,136-13,745,136 ESF1
    nsv5327208copy number variation1nstd204human GRCh38.p13 chr20: 13,618,297-14,410,459 , GRCh37.p13 chr20: 13,598,944-14,391,105 RPS3P1, SEL1L2, 10 more genes
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