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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7070730inversion1nstd229human GRCh38 chr9: 62,058,130-67,204,238 , GRCh37.p13 chr9: 41,204,320-44,676,072 ATP5F1AP10, IGKV1OR9-1, 125 more genes
    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
    nsv6452699copy number variation1nstd223human GRCh38 chr9: 66,147,501-66,175,200 , GRCh37.p13 chr9: 43,128,079-43,155,778 ANKRD20A3P, LOC642929
    nsv6451349copy number variation1nstd223human GRCh38 chr9: 66,145,401-66,158,600 , GRCh37.p13 chr9: 43,125,979-43,139,178 LOC642929, ANKRD20A3P
    nsv6449444copy number variation1nstd223human GRCh38 chr9: 66,145,201-66,203,500 , GRCh37.p13 chr9: 43,125,779-43,184,078 ANKRD20A3P, LOC642929, 1 more genes
    nsv6448624copy number variation1nstd223human GRCh38 chr9: 66,163,101-66,166,000 , GRCh37.p13 chr9: 43,143,679-43,146,578 LOC642929
    nsv6448028copy number variation1nstd223human GRCh38 chr9: 66,151,701-66,175,300 , GRCh37.p13 chr9: 43,132,279-43,155,878 LOC642929, ANKRD20A3P
    nsv6447630copy number variation1nstd223human GRCh38 chr9: 66,144,601-66,158,800 , GRCh37.p13 chr9: 43,125,179-43,139,378 ANKRD20A3P, LOC642929
    nsv6447404copy number variation1nstd223human GRCh38 chr9: 66,148,001-66,176,000 , GRCh37.p13 chr9: 43,128,579-43,156,578 LOC642929, ANKRD20A3P
    nsv6445609copy number variation1nstd223human GRCh38 chr9: 66,146,601-66,173,800 , GRCh37.p13 chr9: 43,127,179-43,154,378 LOC642929, ANKRD20A3P
    nsv6444423copy number variation1nstd223human GRCh38 chr9: 66,146,901-66,176,400 , GRCh37.p13 chr9: 43,127,479-43,156,978 ANKRD20A3P, LOC642929
    nsv6442398copy number variation1nstd223human GRCh38 chr9: 66,147,801-66,202,700 , GRCh37.p13 chr9: 43,128,379-43,183,278 ANKRD20A3P, MEP1AP3, 1 more genes
    nsv6438651copy number variation1nstd223human GRCh38 chr9: 66,146,501-66,202,100 , GRCh37.p13 chr9: 43,127,079-43,182,678 ANKRD20A3P, LOC642929, 1 more genes
    nsv6315415copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-68,342,786 , GRCh38.p12 chr9: 203,861-67,920,552 LOC107987068, FAM74A7, 846 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
    nsv6290004inversion1nstd102humanLikely pathogenic GRCh38.p12 chr9: 12,246,100-98,797,096 , GRCh37 chr9: 12,246,100-101,559,378 ACO1, PLIN2, 1215 more genes
    nsv6142272copy number variation1nstd206human GRCh38 chr9: 66,147,191-66,172,191 , GRCh37.p13 chr9: 43,127,769-43,152,769 LOC642929, ANKRD20A3P
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