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Items: 1 to 20 of 167

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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
    nsv6875175copy number variation1nstd229human GRCh38 chr9: 92,337,320-92,458,659 , GRCh37.p13 chr9: 95,099,602-95,220,941 ASPN, CENPP, 3 more genes
    nsv6871993copy number variation1nstd229human GRCh38 chr9: 92,364,249-92,536,252 , GRCh37.p13 chr9: 95,126,531-95,298,534 ECM2, OGN, 4 more genes
    nsv6871346copy number variation1nstd229human GRCh38 chr9: 92,392,301-92,486,600 , GRCh37.p13 chr9: 95,154,583-95,248,882 ASPN, CENPP, 2 more genes
    nsv6870487copy number variation1nstd229human GRCh38 chr9: 91,906,361-92,583,443 , GRCh37.p13 chr9: 94,668,643-95,345,725 ROR2, LOC100420779, 25 more genes
    nsv6869562copy number variation1nstd229human GRCh38 chr9: 92,415,436-92,472,304 , GRCh37.p13 chr9: 95,177,718-95,234,586 OMD, CENPP, 1 more genes
    nsv6860302copy number variation1nstd229human GRCh38 chr9: 92,429,203-92,460,342 , GRCh37.p13 chr9: 95,191,485-95,222,624 ASPN, CENPP
    nsv6638032copy number variation1nstd102humanUncertain significance GRCh37 chr9: 95,076,710-95,263,214 , GRCh38.p12 chr9: 92,314,428-92,500,932 OMD, CENPP, 5 more genes
    nsv6637685copy number variation1nstd102humanUncertain significance GRCh37 chr9: 94,666,958-95,339,157 , GRCh38.p12 chr9: 91,904,676-92,576,875 ECM2, IARS1, 25 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
    nsv6556992inversion1nstd223human GRCh38 chr9: 92,471,137-92,472,608 , GRCh37.p13 chr9: 95,233,419-95,234,890 ASPN, CENPP
    nsv6556848inversion1nstd223human GRCh38 chr9: 90,743,255-92,932,434 , GRCh37.p13 chr9: 93,505,537-95,694,716 MIR3651, IARS1, 54 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
    nsv6314034copy number variation1nstd102humanUncertain significance GRCh37 chr9: 95,174,066-95,242,960 , GRCh38.p12 chr9: 92,411,784-92,480,678 OMD, ASPN, 1 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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