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Items: 1 to 20 of 169

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7071727inversion1nstd229human GRCh38 chr9: 93,332,022-93,605,636 , GRCh37.p13 chr9: 96,094,304-96,367,918 FAM120AOS, FAM120A2P, 6 more genes
    nsv6877143copy number variation1nstd229human GRCh38 chr9: 93,339,560-93,340,986 , GRCh37.p13 chr9: 96,101,842-96,103,268 FAM120A2P
    nsv6873515copy number variation1nstd229human GRCh38 chr9: 93,265,667-93,357,205 , GRCh37.p13 chr9: 96,027,949-96,119,487 WNK2, FAM120A2P
    nsv6863602copy number variation1nstd229human GRCh38 chr9: 93,337,197-93,344,887 , GRCh37.p13 chr9: 96,099,479-96,107,169 FAM120A2P
    nsv6861114copy number variation1nstd229human GRCh38 chr9: 93,309,201-93,391,052 , GRCh37.p13 chr9: 96,071,483-96,153,334 RNU6-829P, WNK2, 1 more genes
    nsv6860469copy number variation1nstd229human GRCh38 chr9: 93,307,384-93,370,857 , GRCh37.p13 chr9: 96,069,666-96,133,139 FAM120A2P, WNK2
    nsv6637944copy number variation1nstd102humanPathogenic GRCh37 chr9: 95,711,603-98,469,214 , GRCh38.p12 chr9: 92,949,321-95,706,932 MIRLET7D, MIR24-1, 60 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
    nsv6560549inversion1nstd223human GRCh38 chr9: 93,328,304-93,329,006 , GRCh37.p13 chr9: 96,090,586-96,091,288 FAM120A2P
    nsv6453736copy number variation1nstd223human GRCh38 chr9: 93,265,661-93,357,205 , GRCh37.p13 chr9: 96,027,943-96,119,487 FAM120A2P, WNK2
    nsv6447755copy number variation1nstd223human GRCh38 chr9: 92,901,749-100,255,234 , GRCh37.p13 chr9: 95,664,031-103,017,516 EIF4BP3, VN1R51P, 162 more genes
    nsv6442511copy number variation1nstd223human GRCh38 chr9: 93,346,007-93,348,304 , GRCh37.p13 chr9: 96,108,289-96,110,586 FAM120A2P
    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
    nsv6302831copy number variation1nstd186human GRCh37 chr9: 96,090,414-96,090,569 , GRCh38.p12 chr9: 93,328,132-93,328,287 FAM120A2P
    nsv6290004inversion1nstd102humanLikely pathogenic GRCh38.p12 chr9: 12,246,100-98,797,096 , GRCh37 chr9: 12,246,100-101,559,378 ACO1, PLIN2, 1215 more genes
    nsv6180435copy number variation1nstd214human GRCh38 chr9: 93,326,878-93,326,941 , GRCh37.p13 chr9: 96,089,160-96,089,223 WNK2, FAM120A2P
    nsv6136400copy number variation1nstd213human GRCh37 chr9: 95,630,000-96,300,001 , GRCh38.p12 chr9: 92,867,718-93,537,719 NINJ1, ZNF484, 15 more genes
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