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Items: 1 to 20 of 248

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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
    nsv7067414inversion1nstd229human GRCh38 chr9: 33,581,189-33,598,965 , GRCh37.p13 chr9: 33,581,187-33,598,963 CYP4F26P
    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
    nsv6875895copy number variation1nstd229human GRCh38 chr9: 33,587,768-33,588,587 , GRCh37.p13 chr9: 33,587,766-33,588,585 CYP4F26P
    nsv6875391copy number variation1nstd229human GRCh38 chr9: 33,604,180-33,604,594 , GRCh37.p13 chr9: 33,604,178-33,604,592 CYP4F26P
    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
    nsv6869536copy number variation1nstd229human GRCh38 chr9: 33,598,319-33,615,386 , GRCh37.p13 chr9: 33,598,317-33,615,384 CYP4F26P, PRSS3P4
    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
    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
    nsv6560363inversion1nstd223human GRCh38 chr9: 33,533,993-38,610,852 , GRCh37.p13 chr9: 33,533,991-38,610,849 PHF24, CNTFR, 182 more genes
    nsv6453588copy number variation1nstd223human GRCh38 chr9: 33,604,179-33,604,668 , GRCh37.p13 chr9: 33,604,177-33,604,666 CYP4F26P
    nsv6452596copy number variation1nstd223human GRCh38 chr9: 33,602,474-33,744,291 , GRCh37.p13 chr9: 33,602,472-33,744,289 TRBV23OR9-2, PTENP1, 12 more genes
    nsv6449107copy number variation1nstd223human GRCh38 chr9: 33,586,693-33,589,804 , GRCh37.p13 chr9: 33,586,691-33,589,802 CYP4F26P
    nsv6446703copy number variation1nstd223human GRCh38 chr9: 33,588,001-33,597,300 , GRCh37.p13 chr9: 33,587,999-33,597,298 CYP4F26P
    nsv6441048copy number variation1nstd223human GRCh38 chr9: 33,579,017-33,581,959 , GRCh37.p13 chr9: 33,579,015-33,581,957 CYP4F26P
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