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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
    nsv7098082copy number variation1nstd102humanUncertain significance GRCh37 chr9: 34,370,797-36,276,941 , GRCh38.p12 chr9: 34,370,799-36,276,944 UNC13B, CD72, 86 more genes
    nsv7077787inversion1nstd229human GRCh38 chr9: 36,095,897-37,616,085 , GRCh37.p13 chr9: 36,095,894-37,616,082 RPL21P83, MRPS21P4, 33 more genes
    nsv7060440inversion1nstd229human GRCh38 chr9: 33,533,890-38,610,880 , GRCh37.p13 chr9: 33,533,888-38,610,877 FRMPD1, PTENP1, 182 more genes
    nsv7058978inversion1nstd229human GRCh38 chr9: 33,570,636-38,550,207 , GRCh37.p13 chr9: 33,570,634-38,550,204 TRBV29OR9-2, SPMIP6, 180 more genes
    nsv6877925copy number variation1nstd229human GRCh38 chr9: 36,098,252-36,098,306 , GRCh37.p13 chr9: 36,098,249-36,098,303 RECK
    nsv6877026copy number variation1nstd229human GRCh38 chr9: 36,119,772-36,176,364 , GRCh37.p13 chr9: 36,119,769-36,176,361 CCIN, GLIPR2, 1 more genes
    nsv6875958copy number variation1nstd229human GRCh38 chr9: 36,119,475-36,119,913 , GRCh37.p13 chr9: 36,119,472-36,119,910 RECK
    nsv6873609copy number variation1nstd229human GRCh38 chr9: 36,031,702-36,038,294 , GRCh37.p13 chr9: 36,031,699-36,038,291 RECK
    nsv6867371copy number variation1nstd229human GRCh38 chr9: 36,068,707-36,068,810 , GRCh37.p13 chr9: 36,068,704-36,068,807 RECK
    nsv6864316copy number variation1nstd229human GRCh38 chr9: 36,090,854-36,097,518 , GRCh37.p13 chr9: 36,090,851-36,097,515 RECK
    nsv6862624copy number variation1nstd229human GRCh38 chr9: 36,099,325-36,106,378 , GRCh37.p13 chr9: 36,099,322-36,106,375 RECK
    nsv6862066copy number variation1nstd229human GRCh38 chr9: 36,062,540-36,069,669 , GRCh37.p13 chr9: 36,062,537-36,069,666 RECK
    nsv6860656copy number variation1nstd229human GRCh38 chr9: 36,098,194-36,103,170 , GRCh37.p13 chr9: 36,098,191-36,103,167 RECK
    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
    nsv6633454copy number variation1nstd224human GRCh37 chr9: 36,083,430-36,105,264 , GRCh38.p12 chr9: 36,083,433-36,105,267 RECK
    nsv6561046inversion1nstd223human GRCh38 chr9: 36,081,656-36,082,253 , GRCh37.p13 chr9: 36,081,653-36,082,250 RECK
    nsv6560363inversion1nstd223human GRCh38 chr9: 33,533,993-38,610,852 , GRCh37.p13 chr9: 33,533,991-38,610,849 PHF24, CNTFR, 182 more genes
    nsv6559468inversion1nstd223human GRCh38 chr9: 36,062,512-36,063,119 , GRCh37.p13 chr9: 36,062,509-36,063,116 RECK
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