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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7073683inversion1nstd229human GRCh38 chr9: 112,460,277-112,464,169 , GRCh37.p13 chr9: 115,222,557-115,226,449 HSDL2-AS1, HSDL2
    nsv7071138inversion1nstd229human GRCh38 chr9: 112,414,958-112,415,006 , GRCh37.p13 chr9: 115,177,238-115,177,286 HSDL2
    nsv7061375inversion1nstd229human GRCh38 chr9: 111,842,382-112,467,830 , GRCh37.p13 chr9: 114,604,662-115,230,110 RPL29P20, RNU6-710P, 13 more genes
    nsv6875275copy number variation1nstd229human GRCh38 chr9: 112,434,878-112,437,686 , GRCh37.p13 chr9: 115,197,158-115,199,966 HSDL2
    nsv6874743copy number variation1nstd229human GRCh38 chr9: 112,449,293-112,453,774 , GRCh37.p13 chr9: 115,211,573-115,216,054 HSDL2, HSDL2-AS1
    nsv6873362copy number variation1nstd229human GRCh38 chr9: 112,447,046-112,453,298 , GRCh37.p13 chr9: 115,209,326-115,215,578 HSDL2-AS1, HSDL2
    nsv6873070copy number variation1nstd229human GRCh38 chr9: 112,423,778-112,427,118 , GRCh37.p13 chr9: 115,186,058-115,189,398 HSDL2
    nsv6870755copy number variation1nstd229human GRCh38 chr9: 112,445,473-112,448,404 , GRCh37.p13 chr9: 115,207,753-115,210,684 HSDL2
    nsv6870044copy number variation1nstd229human GRCh38 chr9: 112,389,445-112,394,263 , GRCh37.p13 chr9: 115,151,725-115,156,543 HSDL2
    nsv6867898copy number variation1nstd229human GRCh38 chr9: 112,426,001-112,431,300 , GRCh37.p13 chr9: 115,188,281-115,193,580 HSDL2
    nsv6865963copy number variation1nstd229human GRCh38 chr9: 112,418,709-112,418,742 , GRCh37.p13 chr9: 115,180,989-115,181,022 HSDL2
    nsv6863049copy number variation1nstd229human GRCh38 chr9: 112,413,565-112,413,809 , GRCh37.p13 chr9: 115,175,845-115,176,089 HSDL2
    nsv6861452copy number variation1nstd229human GRCh38 chr9: 112,449,528-112,453,771 , GRCh37.p13 chr9: 115,211,808-115,216,051 HSDL2-AS1, HSDL2
    nsv6859999copy number variation1nstd229human GRCh38 chr9: 112,465,367-112,465,603 , GRCh37.p13 chr9: 115,227,647-115,227,883 HSDL2-AS1, HSDL2
    nsv6858096copy number variation1nstd229human GRCh38 chr9: 112,376,609-112,379,622 , GRCh37.p13 chr9: 115,138,889-115,141,902 HSDL2
    nsv6634454copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-131,603,223 , GRCh38.p12 chr9: 203,861-128,840,944 HNRNPA1P41, GAS1RR, 1868 more genes
    nsv6574677inversion1nstd223human GRCh38 chr9: 112,430,781-112,431,966 , GRCh37.p13 chr9: 115,193,061-115,194,246 HSDL2
    nsv6573167inversion1nstd223human GRCh38 chr9: 112,381,377-112,381,961 , GRCh37.p13 chr9: 115,143,657-115,144,241 HSDL2
    nsv6571616inversion1nstd223human GRCh38 chr9: 112,389,921-112,390,646 , GRCh37.p13 chr9: 115,152,201-115,152,926 HSDL2
    nsv6570569inversion1nstd223human GRCh38 chr9: 112,460,462-112,461,378 , GRCh37.p13 chr9: 115,222,742-115,223,658 HSDL2-AS1, HSDL2
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