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Items: 1 to 20 of 211

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7056811inversion1nstd229human GRCh38 chr6: 26,396,056-26,438,859 , GRCh37.p13 chr6: 26,396,284-26,439,087 BTN3A3, BTN3A1, 1 more genes
    nsv7045802inversion1nstd229human GRCh38 chr6: 26,398,011-26,458,240 , GRCh37.p13 chr6: 26,398,239-26,458,468 BTN3A3, BTN2A1, 2 more genes
    nsv6789669copy number variation1nstd229human GRCh38 chr6: 25,978,117-26,742,203 , GRCh37.p13 chr6: 25,978,345-26,585,842 H2AC8, BTN1A1P1, 93 more genes
    nsv6783362copy number variation1nstd229human GRCh38 chr6: 26,321,412-26,533,751 , GRCh37.p13 chr6: 26,321,640-26,533,979 BTN2A1, RNU6-502P, 19 more genes
    nsv6631231copy number variation1nstd224human GRCh37 chr6: 26,382,765-26,452,098 , GRCh38.p12 chr6: 26,382,537-26,451,870 BTN3A3, BTN2A2, 2 more genes
    nsv6630955copy number variation1nstd224human GRCh37 chr6: 26,370,616-26,405,835 , GRCh38.p12 chr6: 26,370,388-26,405,607 BTN3A2, BTN3A1, 1 more genes
    nsv6563406inversion1nstd223human GRCh38 chr6: 25,888,425-29,704,317 , GRCh37.p13 chr6: 25,888,653-29,672,094 OR1F12P, H4C2, 362 more genes
    nsv5889708copy number variation1nstd209human GRCh38 chr6: 26,403,214-26,403,348 , GRCh37.p13 chr6: 26,403,442-26,403,576 BTN3A1
    nsv5685161mobile element insertion1nstd211human GRCh38 chr6: 26,404,347-26,404,347 , GRCh37.p13 chr6: 26,404,575-26,404,575 BTN3A1
    nsv5472333copy number variation1nstd206human GRCh38 chr6: 26,368,000-26,443,500 , GRCh37.p13 chr6: 26,368,228-26,443,728 BTN3A1, BTN2A3P, 3 more genes
    nsv5470413copy number variation1nstd206human GRCh38 chr6: 26,403,203-26,403,369 , GRCh37.p13 chr6: 26,403,431-26,403,597 BTN3A1
    nsv5466978copy number variation1nstd206human GRCh38 chr6: 26,368,000-26,406,000 , GRCh37.p13 chr6: 26,368,228-26,406,228 BTN3A2, BTN2A2, 1 more genes
    nsv5460417copy number variation1nstd206human GRCh38 chr6: 26,369,000-26,406,000 , GRCh37.p13 chr6: 26,369,228-26,406,228 BTN3A1, BTN2A2, 1 more genes
    nsv5409904mobile element insertion1nstd206human GRCh38 chr6: 26,404,347-26,404,351 , GRCh37.p13 chr6: 26,404,575-26,404,579 BTN3A1
    nsv5235756copy number variation1nstd204human GRCh38.p13 chr6: 26,407,192-26,411,779 , GRCh37.p13 chr6: 26,407,420-26,412,007 BTN3A1
    nsv5235618copy number variation1nstd204human GRCh38.p13 chr6: 26,404,592-26,406,591 , GRCh37.p13 chr6: 26,404,820-26,406,819 BTN3A1
    nsv5230609copy number variation1nstd204human GRCh38.p13 chr6: 26,366,962-26,406,791 , GRCh37.p13 chr6: 26,367,190-26,407,019 BTN3A1, BTN2A2, 1 more genes
    nsv5230539copy number variation1nstd204human GRCh38.p13 chr6: 26,400,942-26,405,988 , GRCh37.p13 chr6: 26,401,170-26,406,216 BTN3A1
    nsv5228655copy number variation1nstd204human GRCh38.p13 chr6: 26,408,392-26,409,691 , GRCh37.p13 chr6: 26,408,620-26,409,919 BTN3A1
    nsv5221347copy number variation1nstd204human GRCh38.p13 chr6: 26,368,601-26,406,000 , GRCh37.p13 chr6: 26,368,829-26,406,228 BTN3A1, BTN2A2, 1 more genes
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