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Items: 1 to 20 of 211

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7098455copy number variation6nstd102humanUncertain significance GRCh37 chr9: 32,453,279-37,785,041 , GRCh38.p12 chr9: 32,453,281-37,785,044 TRBVAOR9-2, UBAP2, 197 more genes
    nsv7098080copy number variation1nstd102humanUncertain significance GRCh37 chr9: 32,453,279-35,068,379 , GRCh38.p12 chr9: 32,453,281-35,068,382 SUGT1P1, RNU7-36P, 110 more genes
    nsv6871636copy number variation1nstd229human GRCh38 chr9: 33,220,908-33,499,144 , GRCh37.p13 chr9: 33,220,906-33,499,142 AQP3, NFX1, 11 more genes
    nsv6868978copy number variation1nstd229human GRCh38 chr9: 33,282,362-33,282,430 , GRCh37.p13 chr9: 33,282,360-33,282,428 CHMP5
    nsv6637410copy number variation1nstd102humanUncertain significance GRCh37 chr9: 33,127,803-33,398,500 , GRCh38.p12 chr9: 33,127,805-33,398,502 SPINK4, LOC100862682, 8 more genes
    nsv6637186copy number variation1nstd102humanUncertain significance GRCh37 chr9: 33,127,803-33,391,202 , GRCh38.p12 chr9: 33,127,805-33,391,204 B4GALT1, LOC105376018, 8 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
    nsv6634409copy number variation1nstd102humanLikely pathogenic GRCh37 chr9: 1-40,036,525 , GRCh38.p12 chr9: 10,001-39,445,729 ACO1, PLIN2, 594 more genes
    nsv6633988copy number variation1nstd224human GRCh37 chr9: 33,097,996-33,276,564 , GRCh38.p12 chr9: 33,097,998-33,276,566 BAG1, B4GALT1, 5 more genes
    nsv6565815inversion1nstd223human GRCh38 chr9: 33,279,063-33,279,864 , GRCh37.p13 chr9: 33,279,061-33,279,862 CHMP5
    nsv6562397inversion1nstd223human GRCh38 chr9: 33,279,596-33,280,048 , GRCh37.p13 chr9: 33,279,594-33,280,046 CHMP5
    nsv6450204copy number variation1nstd223human GRCh38 chr9: 33,086,071-33,276,676 , GRCh37.p13 chr9: 33,086,069-33,276,674 B4GALT1-AS1, MIR12117, 5 more genes
    nsv6315463copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-35,903,398 , GRCh38.p12 chr9: 203,861-35,903,401 IFNA11P, RNU6-14P, 495 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
    nsv6313892copy number variation1nstd102humanPathogenic GRCh37 chr9: 676,264-33,743,670 , GRCh38.p12 chr9: 676,264-33,743,672 SUGT1P1, FOCAD-AS1, 391 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
    nsv6137461copy number variation1nstd213human GRCh37 chr9: 32,140,000-33,310,001 , GRCh38.p12 chr9: 32,140,002-33,310,003 ACO1, BAG1, 31 more genes
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