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Items: 1 to 20 of 188

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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
    nsv7093502insertion1nstd102humanUncertain significance GRCh37 chr9: 35,657,799-35,657,799 , GRCh38 chr9: 35,657,802-35,657,802 RMRP, ARHGEF39, 1 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
    nsv6870133copy number variation1nstd229human GRCh38 chr9: 34,043,094-35,876,103 , GRCh37.p13 chr9: 34,043,092-35,876,100 STOML2, ENHO, 85 more genes
    nsv6869578copy number variation1nstd229human GRCh38 chr9: 35,657,732-35,657,802 , GRCh37.p13 chr9: 35,657,729-35,657,799 RMRP, CCDC107, 1 more genes
    nsv6869004copy number variation1nstd229human GRCh38 chr9: 35,529,901-35,865,200 , GRCh37.p13 chr9: 35,529,898-35,865,197 TESK1, MIR4667, 25 more genes
    nsv6863079copy number variation1nstd229human GRCh38 chr9: 35,616,001-35,699,200 , GRCh37.p13 chr9: 35,615,998-35,699,197 TPM2, RN7SL22P, 8 more genes
    nsv6862865copy number variation1nstd229human GRCh38 chr9: 35,643,801-35,656,300 , GRCh37.p13 chr9: 35,643,798-35,656,297 SIT1, RMRP, 2 more genes
    nsv6862579copy number variation1nstd229human GRCh38 chr9: 35,546,901-35,914,300 , GRCh37.p13 chr9: 35,546,898-35,914,297 RPS29P17, CCDC107, 29 more genes
    nsv6860777copy number variation1nstd229human GRCh38 chr9: 35,657,841-35,674,980 , GRCh37.p13 chr9: 35,657,838-35,674,977 CCDC107, RMRP, 3 more genes
    nsv6859169copy number variation1nstd229human GRCh38 chr9: 35,518,501-35,914,400 , GRCh37.p13 chr9: 35,518,498-35,914,397 GBA2, CREB3, 29 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
    nsv6633453copy number variation1nstd224human GRCh37 chr9: 35,649,916-35,674,347 , GRCh38.p12 chr9: 35,649,919-35,674,350 CA9, RMRP, 4 more genes
    nsv6560363inversion1nstd223human GRCh38 chr9: 33,533,993-38,610,852 , GRCh37.p13 chr9: 33,533,991-38,610,849 PHF24, CNTFR, 182 more genes
    nsv6440919copy number variation1nstd223human GRCh38 chr9: 35,658,201-35,658,800 , GRCh37.p13 chr9: 35,658,198-35,658,797 ARHGEF39, RMRP, 1 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
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