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Items: 1 to 20 of 323

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7147866insertion1nstd232human GRCh38.p12 chr9: 33,574,116-33,574,116 , GRCh37.p13 chr9: 33,574,114-33,574,114 bA255A11.4, ANKRD18B, 1 more genes
    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
    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
    nsv6873856copy number variation1nstd229human GRCh38 chr9: 33,535,101-33,540,300 , GRCh37.p13 chr9: 33,535,099-33,540,298 ANKRD18B
    nsv6870150copy number variation1nstd229human GRCh38 chr9: 33,490,104-33,625,553 , GRCh37.p13 chr9: 33,490,102-33,625,551 PRSS3P4, ANKRD18B, 8 more genes
    nsv6865806copy number variation1nstd229human GRCh38 chr9: 33,536,154-33,540,311 , GRCh37.p13 chr9: 33,536,152-33,540,309 ANKRD18B
    nsv6861860copy number variation1nstd229human GRCh38 chr9: 33,561,458-33,566,733 , GRCh37.p13 chr9: 33,561,456-33,566,731 ANKRD18B
    nsv6861157copy number variation1nstd229human GRCh38 chr9: 33,498,978-33,603,950 , GRCh37.p13 chr9: 33,498,976-33,603,948 ANKRD18B, VN1R47P, 4 more genes
    nsv6860138copy number variation1nstd229human GRCh38 chr9: 33,573,405-33,574,218 , GRCh37.p13 chr9: 33,573,403-33,574,216 ANKRD18B, SNX18P7, 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
    nsv6633516copy number variation1nstd224human GRCh37 chr9: 33,343,397-33,700,901 , GRCh38.p12 chr9: 33,343,399-33,700,903 NFX1, TRBV24OR9-2, 24 more genes
    nsv6563801inversion1nstd223human GRCh38 chr9: 33,569,505-33,569,831 , GRCh37.p13 chr9: 33,569,503-33,569,829 ANKRD18B
    nsv6560363inversion1nstd223human GRCh38 chr9: 33,533,993-38,610,852 , GRCh37.p13 chr9: 33,533,991-38,610,849 PHF24, CNTFR, 182 more genes
    nsv6454951copy number variation1nstd223human GRCh38 chr9: 33,507,801-33,530,400 , GRCh37.p13 chr9: 33,507,799-33,530,398 SUGT1P1, ANKRD18B, 1 more genes
    nsv6452738copy number variation1nstd223human GRCh38 chr9: 33,573,403-33,574,215 , GRCh37.p13 chr9: 33,573,401-33,574,213 bA255A11.4, ANKRD18B, 1 more genes
    nsv6448434copy number variation1nstd223human GRCh38 chr9: 33,566,201-33,567,300 , GRCh37.p13 chr9: 33,566,199-33,567,298 ANKRD18B
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