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Items: 1 to 20 of 335

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7145899copy number variation1nstd232human GRCh37.p13 chr14: 102,493,879-102,493,952 , GRCh38.p12 chr14: 102,027,542-102,027,615 DYNC1H1
    nsv7145447copy number variation1nstd232human GRCh37.p13 chr14: 102,511,727-102,511,793 , GRCh38.p12 chr14: 102,045,390-102,045,456 DYNC1H1
    nsv7145222copy number variation1nstd232human GRCh37.p13 chr14: 102,493,623-102,493,716 , GRCh38.p12 chr14: 102,027,286-102,027,379 DYNC1H1
    nsv7142781copy number variation1nstd232human GRCh37.p13 chr14: 102,461,431-102,461,514 , GRCh38.p12 chr14: 101,995,094-101,995,177 DYNC1H1
    nsv7142606insertion1nstd232human GRCh37.p13 chr14: 102,460,664-102,460,664 , GRCh38.p12 chr14: 101,994,327-101,994,327 DYNC1H1
    nsv7141084copy number variation1nstd232human GRCh37.p13 chr14: 102,510,826-102,510,928 , GRCh38.p12 chr14: 102,044,489-102,044,591 DYNC1H1
    nsv7139863copy number variation1nstd232human GRCh37.p13 chr14: 102,483,628-102,483,715 , GRCh38.p12 chr14: 102,017,291-102,017,378 DYNC1H1
    nsv7094416copy number variation1nstd102humanUncertain significance GRCh37 chr14: 102,460,501-102,516,900 , GRCh38.p12 chr14: 101,994,164-102,050,563 LOC107984661, DYNC1H1
    nsv7094321copy number variation1nstd102humanUncertain significance GRCh37 chr14: 102,463,352-102,469,322 , GRCh38.p12 chr14: 101,997,015-102,002,985 DYNC1H1
    nsv7094241copy number variation1nstd102humanUncertain significance GRCh37 chr14: 102,442,029-105,861,009 , GRCh38.p12 chr14: 101,975,692-105,394,672 LOC107984670, MARK3, 101 more genes
    nsv7094007copy number variation1nstd102humanUncertain significance GRCh37 chr14: 102,228,231-105,861,009 , GRCh38.p12 chr14: 101,761,894-105,394,672 CLBA1, BAG5, 105 more genes
    nsv6975732copy number variation1nstd229human GRCh38 chr14: 102,054,496-102,056,936 , GRCh37.p13 chr14: 102,520,833-102,523,273 DYNC1H1
    nsv6974960copy number variation1nstd229human GRCh38 chr14: 101,951,186-101,963,847 , GRCh37.p13 chr14: 102,417,523-102,430,184 DYNC1H1
    nsv6971064copy number variation1nstd229human GRCh38 chr14: 101,928,101-102,030,100 , GRCh37.p13 chr14: 102,394,438-102,496,437 PPP2R5C, DYNC1H1
    nsv6966732copy number variation1nstd229human GRCh38 chr14: 102,056,701-102,058,200 , GRCh37.p13 chr14: 102,523,038-102,524,537 DYNC1H1
    nsv6963455copy number variation1nstd229human GRCh38 chr14: 102,051,900-102,056,380 , GRCh37.p13 chr14: 102,518,237-102,522,717 DYNC1H1
    nsv6961917copy number variation1nstd229human GRCh38 chr14: 102,045,391-102,045,457 , GRCh37.p13 chr14: 102,511,728-102,511,794 DYNC1H1
    nsv6960160copy number variation1nstd229human GRCh38 chr14: 102,051,818-102,054,833 , GRCh37.p13 chr14: 102,518,155-102,521,170 DYNC1H1
    nsv6959602copy number variation1nstd229human GRCh38 chr14: 102,044,700-102,047,818 , GRCh37.p13 chr14: 102,511,037-102,514,155 DYNC1H1
    nsv6958490copy number variation1nstd229human GRCh38 chr14: 102,046,513-102,046,545 , GRCh37.p13 chr14: 102,512,850-102,512,882 DYNC1H1
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