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Items: 1 to 20 of 177

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7098477copy number variation1nstd102humanPathogenic GRCh37 chr9: 94,485,944-95,527,026 , GRCh38.p12 chr9: 91,723,662-92,764,744 LINC00475, MTATP6P29, 30 more genes
    nsv7075105inversion1nstd229human GRCh38 chr9: 92,721,873-92,725,847 , GRCh37.p13 chr9: 95,484,155-95,488,129 BICD2
    nsv7070126inversion1nstd229human GRCh38 chr9: 92,739,602-92,881,693 , GRCh37.p13 chr9: 95,501,884-95,643,975 BICD2, ZNF484, 6 more genes
    nsv6875258copy number variation1nstd229human GRCh38 chr9: 92,763,138-92,856,884 , GRCh37.p13 chr9: 95,525,420-95,619,166 RNU6-714P, LOC101929748, 5 more genes
    nsv6869018copy number variation1nstd229human GRCh38 chr9: 92,736,354-92,744,491 , GRCh37.p13 chr9: 95,498,636-95,506,773 BICD2
    nsv6867348copy number variation1nstd229human GRCh38 chr9: 92,720,681-92,720,993 , GRCh37.p13 chr9: 95,482,963-95,483,275 BICD2
    nsv6863040copy number variation1nstd229human GRCh38 chr9: 92,729,438-92,734,284 , GRCh37.p13 chr9: 95,491,720-95,496,566 BICD2
    nsv6859741copy number variation1nstd229human GRCh38 chr9: 92,599,301-92,808,400 , GRCh37.p13 chr9: 95,361,583-95,570,682 ANKRD19P, LOC101929748, 6 more genes
    nsv6637423copy number variation1nstd102humanUncertain significance GRCh37 chr9: 95,079,794-95,503,060 , GRCh38.p12 chr9: 92,317,512-92,740,778 IPPK, LOC100420779, 11 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
    nsv6633497copy number variation1nstd224human GRCh37 chr9: 94,927,564-95,560,534 , GRCh38.p12 chr9: 92,165,282-92,798,252 IPPK, IARS1, 17 more genes
    nsv6569472inversion1nstd223human GRCh38 chr9: 92,753,547-92,754,023 , GRCh37.p13 chr9: 95,515,829-95,516,305 BICD2
    nsv6556848inversion1nstd223human GRCh38 chr9: 90,743,255-92,932,434 , GRCh37.p13 chr9: 93,505,537-95,694,716 MIR3651, IARS1, 54 more genes
    nsv6452522copy number variation1nstd223human GRCh38 chr9: 92,756,201-92,757,800 , GRCh37.p13 chr9: 95,518,483-95,520,082 BICD2
    nsv6437148copy number variation1nstd223human GRCh38 chr9: 92,745,693-92,896,447 , GRCh37.p13 chr9: 95,507,975-95,658,729 ZNF484, EEF1DP2, 7 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
    nsv6315179copy number variation1nstd102humanPathogenic GRCh37 chr9: 93,864,974-106,661,581 , GRCh38.p12 chr9: 91,102,692-103,899,300 SUGT1P4-STRA6LP, NR4A3, 255 more genes
    nsv6313900copy number variation1nstd102humanLikely pathogenic GRCh37 chr9: 71,349,994-122,603,410 , GRCh38.p12 chr9: 68,735,078-119,841,132 ABCA1, ALAD, 793 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
    nsv6313293copy number variation2nstd102humanUncertain significance GRCh37 chr9: 94,794,747-95,527,026 , GRCh38.p12 chr9: 92,032,465-92,764,744 SNORA84, IARS1, 25 more genes
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