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Items: 1 to 20 of 121

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7064084inversion1nstd229human GRCh38 chr9: 64,120,773-68,530,496 , GRCh37.p13 chr9: 40,041,911-44,672,613 LOC112267859, ZNG1C, 91 more genes
    nsv6634454copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-131,603,223 , GRCh38.p12 chr9: 203,861-128,840,944 HNRNPA1P41, GAS1RR, 1868 more genes
    nsv6315405copy number variation1nstd102humanUncertain significance GRCh37 chr9: 19,356,861-119,513,311 , GRCh38.p12 chr9: 19,356,863-116,751,032 RNU6-156P, GDA, 1425 more genes
    nsv6313827copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-84,155,399 , GRCh38.p12 chr9: 203,861-81,540,484 RPSAP75, ANKRD20A2P, 1008 more genes
    nsv6313546copy number variation1nstd102humanPathogenic GRCh37 chr9: 353,349-141,020,389 , GRCh38.p12 chr9: 353,349-138,125,937 FAM27C, DPM2, 2166 more genes
    nsv6300760copy number variation1nstd186human GRCh37 chr9: 70,907,468-70,952,616 , GRCh38.p12 chr9: 68,292,552-68,337,700 FOXD4L3, ZNG1C, 2 more genes
    nsv6290004inversion1nstd102humanLikely pathogenic GRCh38.p12 chr9: 12,246,100-98,797,096 , GRCh37 chr9: 12,246,100-101,559,378 ACO1, PLIN2, 1215 more genes
    nsv6142925copy number variation1nstd206human GRCh37.p13 chr9|NW_003871067.1: 72,000-117,148 , GRCh38 chr9: 68,292,552-68,337,700 , GRCh37.p13 chr9: 70,907,468-70,952,616 LOC101929800, FOXD4L3, 2 more genes
    nsv6141980copy number variation1nstd206human GRCh37.p13 chr9|NW_003871067.1: 14,111-108,724 , GRCh38 chr9: 68,234,663-68,329,276 , GRCh37.p13 chr9: 70,849,579-70,944,192 ZNG1C, FOXD4L3, 2 more genes
    nsv6097330insertion1nstd212human GRCh38 chr9: 68,301,592-68,301,592 , GRCh37.p13 chr9|NW_003871067.1: 81,040-81,040 , GRCh37.p13 chr9: 70,916,508-70,916,508 FOXD4L3
    nsv5637746insertion1nstd207human GRCh38 chr9: 68,301,572-68,301,572 , GRCh37.p13 chr9: 70,916,488-70,916,488 , GRCh37.p13 chr9|NW_003871067.1: 81,020-81,020 FOXD4L3
    nsv5474068copy number variation1nstd206human GRCh38 chr9: 68,301,910-68,301,979 , GRCh37.p13 chr9|NW_003871067.1: 81,358-81,427 , GRCh37.p13 chr9: 70,916,826-70,916,895 FOXD4L3
    nsv5257784copy number variation1nstd204human GRCh38.p13 chr9: 68,294,001-68,302,000 , GRCh37.p13 chr9: 70,908,917-70,916,916 , GRCh37.p13 chr9|NW_003871067.1: 73,449-81,448 ZNG1C, FOXD4L3
    nsv5257579copy number variation1nstd204human GRCh38.p13 chr9: 68,287,001-68,309,500 , GRCh37.p13 chr9: 70,901,917-70,924,416 , GRCh37.p13 chr9|NW_003871067.1: 66,449-88,948 ZNG1C, FOXD4L3, 1 more genes
    nsv5254812copy number variation1nstd204human GRCh38.p13 chr9: 68,292,101-68,311,500 , GRCh37.p13 chr9|NW_003871067.1: 71,549-90,948 , GRCh37.p13 chr9: 70,907,017-70,926,416 ZNG1C, LOC107987077, 1 more genes
    nsv5254746copy number variation1nstd204human GRCh38.p13 chr9: 68,300,901-68,309,500 , GRCh37.p13 chr9|NW_003871067.1: 80,349-88,948 , GRCh37.p13 chr9: 70,915,817-70,924,416 LOC107987077, FOXD4L3
    nsv5253256copy number variation1nstd204human GRCh38.p13 chr9: 68,291,701-68,309,500 , GRCh37.p13 chr9|NW_003871067.1: 71,149-88,948 , GRCh37.p13 chr9: 70,906,617-70,924,416 LOC107987077, FOXD4L3, 1 more genes
    nsv5248769copy number variation1nstd204human GRCh38.p13 chr9: 68,299,601-68,305,100 , GRCh37.p13 chr9|NW_003871067.1: 79,049-84,548 , GRCh37.p13 chr9: 70,914,517-70,920,016 LOC107987077, FOXD4L3, 1 more genes
    nsv5246424copy number variation1nstd204human GRCh38.p13 chr9: 68,299,601-68,309,500 , GRCh37.p13 chr9|NW_003871067.1: 79,049-88,948 , GRCh37.p13 chr9: 70,914,517-70,924,416 ZNG1C, LOC107987077, 1 more genes
    nsv5245262copy number variation1nstd204human GRCh38.p13 chr9: 68,302,701-68,308,300 , GRCh37.p13 chr9|NW_003871067.1: 82,149-87,748 , GRCh37.p13 chr9: 70,917,617-70,923,216 LOC107987077, FOXD4L3
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