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Items: 1 to 20 of 320

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6115881mobile element insertion1nstd186human GRCh37 chr12: 8,363,593-8,363,644 , GRCh38.p12 chr12: 8,210,997-8,211,048 DEFB109F
    nsv5926703copy number variation1nstd209human GRCh38 chr12: 8,208,854-8,238,297 , GRCh37.p13 chr12: 8,361,450-8,390,893 FAM86FP, LINC02449, 3 more genes
    nsv5866747copy number variation3nstd209human GRCh38 chr12: 8,212,961-8,216,879 , GRCh37.p13 chr12: 8,365,557-8,369,475 DEFB109F
    nsv5696299mobile element insertion2nstd211human GRCh38 chr12: 8,214,634-8,214,634 , GRCh37.p13 chr12: 8,367,230-8,367,230 DEFB109F
    nsv5694454mobile element insertion2nstd211human GRCh38 chr12: 8,210,997-8,210,997 , GRCh37.p13 chr12: 8,363,593-8,363,593 DEFB109F
    nsv5646382insertion1nstd207human GRCh38 chr12: 8,197,802-8,197,802 , GRCh37.p13 chr12: 8,350,398-8,350,398 DEFB109F, FAM66C
    nsv5600586copy number variation1nstd207human GRCh38 chr12: 8,209,697-8,210,016 , GRCh37.p13 chr12: 8,362,293-8,362,612 DEFB109F
    nsv5588751copy number variation1nstd207human GRCh38 chr12: 8,215,108-8,215,187 , GRCh37.p13 chr12: 8,367,704-8,367,783 DEFB109F
    nsv5547418insertion1nstd206human GRCh38 chr12: 8,213,138-8,213,150 , GRCh37.p13 chr12: 8,365,734-8,365,746 DEFB109F
    nsv5509582copy number variation1nstd206human GRCh38 chr12: 8,208,854-8,238,302 , GRCh37.p13 chr12: 8,361,450-8,390,898 FAM86FP, FAM90A1, 3 more genes
    nsv5431117mobile element insertion1nstd206human GRCh38 chr12: 8,210,997-8,211,048 , GRCh37.p13 chr12: 8,363,593-8,363,644 DEFB109F
    nsv5419355mobile element insertion1nstd206human GRCh38 chr12: 8,214,634-8,214,685 , GRCh37.p13 chr12: 8,367,230-8,367,281 DEFB109F
    nsv5392072copy number variation3nstd186human GRCh37 chr12: 8,361,450-8,390,898 , GRCh38.p12 chr12: 8,208,854-8,238,302 FAM90A1, FAM86FP, 3 more genes
    nsv5323122inversion1nstd204human GRCh37.p13 chr12: 6,338,815-22,046,498 , GRCh38.p13 chr12: 6,229,649-21,893,564 , A2M, 414 more genes
    nsv5304595copy number variation1nstd204human GRCh38.p13 chr12: 8,208,853-8,238,303 , GRCh37.p13 chr12: 8,361,449-8,390,899 FAM86FP, FAM90A1, 3 more genes
    nsv5276755copy number variation1nstd204human GRCh38.p13 chr12: 8,208,501-8,238,300 , GRCh37.p13 chr12: 8,361,097-8,390,896 ALG1L10P, LINC02449, 3 more genes
    nsv5276591copy number variation1nstd204human GRCh38.p13 chr12: 8,209,001-8,228,000 , GRCh37.p13 chr12: 8,361,597-8,380,596 ALG1L10P, DEFB109F, 1 more genes
    nsv5272216copy number variation1nstd204human GRCh38.p13 chr12: 8,200,501-8,202,600 , GRCh37.p13 chr12: 8,353,097-8,355,196 FAM66C, DEFB109F
    nsv5268555copy number variation1nstd204human GRCh38.p13 chr12: 8,205,312-8,212,985 , GRCh37.p13 chr12: 8,357,908-8,365,581 DEFB109F
    nsv5264466copy number variation1nstd204human GRCh38.p13 chr12: 8,200,701-8,201,600 , GRCh37.p13 chr12: 8,353,297-8,354,196 FAM66C, DEFB109F
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