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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7138689copy number variation1nstd232human GRCh37.p13 chr17: 75,452,680-75,452,739 , GRCh38.p12 chr17: 77,456,598-77,456,657 SEPTIN9, LOC105371903
    nsv7098776copy number variation1nstd102humanUncertain significance GRCh37 chr17: 75,316,409-75,494,740 , GRCh38.p12 chr17: 77,320,327-77,498,658 LOC112268198, LOC112268199, 3 more genes
    nsv7098764copy number variation1nstd102humanUncertain significance GRCh37 chr17: 75,478,206-75,494,740 , GRCh38.p12 chr17: 77,482,124-77,498,658 SEPTIN9
    nsv7098750copy number variation1nstd102humanUncertain significance GRCh37 chr17: 75,398,121-75,398,805 , GRCh38.p12 chr17: 77,402,039-77,402,723 SEPTIN9
    nsv7098742copy number variation1nstd102humanUncertain significance GRCh37 chr17: 75,398,457-75,398,803 , GRCh38.p12 chr17: 77,402,375-77,402,721 SEPTIN9
    nsv7098713copy number variation1nstd102humanUncertain significance GRCh37 chr17: 75,316,409-75,398,805 , GRCh38.p12 chr17: 77,320,327-77,402,723 MIR4316, SEPTIN9
    nsv7074878inversion1nstd229human GRCh38 chr17: 77,067,592-77,435,829 , GRCh37.p13 chr17: 75,063,674-75,431,911 SNHG20, MIR6516, 10 more genes
    nsv6997924copy number variation1nstd229human GRCh38 chr17: 77,115,680-77,630,885 , GRCh37.p13 chr17: 75,111,762-75,626,967 SEPTIN9, LOC112268199, 11 more genes
    nsv6997409copy number variation1nstd229human GRCh38 chr17: 77,415,079-77,423,325 , GRCh37.p13 chr17: 75,411,161-75,419,407 SEPTIN9
    nsv6997219copy number variation1nstd229human GRCh38 chr17: 77,380,807-77,386,409 , GRCh37.p13 chr17: 75,376,889-75,382,491 SEPTIN9
    nsv6996226copy number variation1nstd229human GRCh38 chr17: 77,493,077-77,498,539 , GRCh37.p13 chr17: 75,489,159-75,494,621 SEPTIN9
    nsv6995616copy number variation1nstd229human GRCh38 chr17: 77,407,171-77,410,974 , GRCh37.p13 chr17: 75,403,253-75,407,056 SEPTIN9
    nsv6995612copy number variation1nstd229human GRCh38 chr17: 77,376,020-77,380,843 , GRCh37.p13 chr17: 75,372,102-75,376,925 SEPTIN9
    nsv6993877copy number variation1nstd229human GRCh38 chr17: 77,481,547-77,481,608 , GRCh37.p13 chr17: 75,477,629-75,477,690 SEPTIN9
    nsv6992404copy number variation1nstd229human GRCh38 chr17: 77,417,185-77,419,314 , GRCh37.p13 chr17: 75,413,267-75,415,396 SEPTIN9
    nsv6991822copy number variation1nstd229human GRCh38 chr17: 77,351,013-77,351,053 , GRCh37.p13 chr17: 75,347,095-75,347,135 SEPTIN9
    nsv6991333copy number variation1nstd229human GRCh38 chr17: 77,372,501-77,373,600 , GRCh37.p13 chr17: 75,368,583-75,369,682 SEPTIN9
    nsv6990799copy number variation1nstd229human GRCh38 chr17: 77,492,226-77,492,369 , GRCh37.p13 chr17: 75,488,308-75,488,451 SEPTIN9
    nsv6990686copy number variation1nstd229human GRCh38 chr17: 77,410,701-77,420,700 , GRCh37.p13 chr17: 75,406,783-75,416,782 SEPTIN9
    nsv6990399copy number variation1nstd229human GRCh38 chr17: 77,308,619-77,313,873 , GRCh37.p13 chr17: 75,304,701-75,309,955 SEPTIN9
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