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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
    nsv7067307inversion1nstd229human GRCh38 chr9: 33,781,635-33,781,812 , GRCh37.p13 chr9: 33,781,633-33,781,810 PRSS3
    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
    nsv7058639inversion1nstd229human GRCh38 chr9: 33,412,279-33,823,665 , GRCh37.p13 chr9: 33,412,277-33,823,663 ANKRD18B, VN1R47P, 24 more genes
    nsv6875535copy number variation1nstd229human GRCh38 chr9: 33,784,144-33,792,849 , GRCh37.p13 chr9: 33,784,142-33,792,847 TRBV29OR9-2, PRSS3
    nsv6873608copy number variation1nstd229human GRCh38 chr9: 33,785,144-33,797,039 , GRCh37.p13 chr9: 33,785,142-33,797,037 PRSS3, TRBV29OR9-2
    nsv6872385copy number variation1nstd229human GRCh38 chr9: 33,746,152-33,754,649 , GRCh37.p13 chr9: 33,746,150-33,754,647 PRSS3
    nsv6870151copy number variation1nstd229human GRCh38 chr9: 33,770,887-33,774,908 , GRCh37.p13 chr9: 33,770,885-33,774,906 PRSS3
    nsv6863748copy number variation1nstd229human GRCh38 chr9: 33,729,867-33,861,178 , GRCh37.p13 chr9: 33,729,865-33,861,176 UBE2R2-AS1, UBE2R2, 2 more genes
    nsv6861819copy number variation1nstd229human GRCh38 chr9: 33,776,211-33,819,583 , GRCh37.p13 chr9: 33,776,209-33,819,581 TRBV29OR9-2, PRSS3, 1 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
    nsv6560363inversion1nstd223human GRCh38 chr9: 33,533,993-38,610,852 , GRCh37.p13 chr9: 33,533,991-38,610,849 PHF24, CNTFR, 182 more genes
    nsv6442003copy number variation1nstd223human GRCh38 chr9: 33,670,403-33,860,450 , GRCh37.p13 chr9: 33,670,401-33,860,448 TRBV29OR9-2, PTENP1, 6 more genes
    nsv6441049copy number variation1nstd223human GRCh38 chr9: 33,767,767-33,770,038 , GRCh37.p13 chr9: 33,767,765-33,770,036 PRSS3
    nsv6438466copy number variation1nstd223human GRCh38 chr9: 33,764,448-33,767,740 , GRCh37.p13 chr9: 33,764,446-33,767,738 PRSS3
    nsv6315572copy number variation1nstd102humanUncertain significance GRCh38 chr9: 33,492,358-34,725,916 , GRCh37.p13 chr9: 33,492,356-34,725,913 PTENP1, KIF24, 60 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
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