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Items: 1 to 20 of 361

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7068293inversion1nstd229human GRCh38 chr9: 12,453,912-21,375,878 , GRCh37.p13 chr9: 12,453,912-21,375,877 RNU6-264P, PSMC3P1, 115 more genes
    nsv6876113copy number variation1nstd229human GRCh38 chr9: 21,181,008-21,228,185 , GRCh37.p13 chr9: 21,181,007-21,228,184 IFNA4, IFNA7, 5 more genes
    nsv6875324copy number variation1nstd229human GRCh38 chr9: 21,193,301-21,213,500 , GRCh37.p13 chr9: 21,193,300-21,213,499 IFNA7, IFNA10, 1 more genes
    nsv6874797copy number variation1nstd229human GRCh38 chr9: 21,192,101-21,212,500 , GRCh37.p13 chr9: 21,192,100-21,212,499 IFNA7, IFNWP18, 1 more genes
    nsv6873832copy number variation1nstd229human GRCh38 chr9: 20,684,201-21,311,600 , GRCh37.p13 chr9: 20,684,200-21,311,599 IFNWP5, IFNWP18, 22 more genes
    nsv6873642copy number variation1nstd229human GRCh38 chr9: 21,193,762-21,212,300 , GRCh37.p13 chr9: 21,193,761-21,212,299 IFNWP18, IFNA10, 1 more genes
    nsv6872666copy number variation1nstd229human GRCh38 chr9: 21,189,138-21,218,660 , GRCh37.p13 chr9: 21,189,137-21,218,659 IFNWP18, IFNA10, 3 more genes
    nsv6871865copy number variation1nstd229human GRCh38 chr9: 21,193,601-21,214,700 , GRCh37.p13 chr9: 21,193,600-21,214,699 IFNA7, IFNWP18, 2 more genes
    nsv6870098copy number variation1nstd229human GRCh38 chr9: 21,191,601-21,212,000 , GRCh37.p13 chr9: 21,191,600-21,211,999 IFNA10, IFNA7, 2 more genes
    nsv6869863copy number variation1nstd229human GRCh38 chr9: 21,190,701-21,212,600 , GRCh37.p13 chr9: 21,190,700-21,212,599 IFNA10, IFNA7, 2 more genes
    nsv6869556copy number variation1nstd229human GRCh38 chr9: 21,133,080-21,557,410 , GRCh37.p13 chr9: 21,133,079-21,557,409 IFNWP19, IFNWP2, 27 more genes
    nsv6867511copy number variation1nstd229human GRCh38 chr9: 21,206,598-21,274,027 , GRCh37.p13 chr9: 21,206,597-21,274,026 LOC107987053, IFNA10, 5 more genes
    nsv6866886copy number variation1nstd229human GRCh38 chr9: 20,629,960-21,204,461 , GRCh37.p13 chr9: 20,629,959-21,204,460 IFNA21, SNORA30B, 14 more genes
    nsv6865375copy number variation1nstd229human GRCh38 chr9: 21,189,569-21,219,032 , GRCh37.p13 chr9: 21,189,568-21,219,031 IFNWP18, IFNA16, 3 more genes
    nsv6864670copy number variation1nstd229human GRCh38 chr9: 21,038,118-21,284,709 , GRCh37.p13 chr9: 21,038,117-21,284,708 IFNWP18, IFNA17, 16 more genes
    nsv6864446copy number variation1nstd229human GRCh38 chr9: 21,193,490-21,212,065 , GRCh37.p13 chr9: 21,193,489-21,212,064 IFNWP18, IFNA10, 1 more genes
    nsv6861654copy number variation1nstd229human GRCh38 chr9: 21,192,301-21,212,300 , GRCh37.p13 chr9: 21,192,300-21,212,299 IFNWP18, IFNA10, 1 more genes
    nsv6859638copy number variation1nstd229human GRCh38 chr9: 21,193,701-21,212,100 , GRCh37.p13 chr9: 21,193,700-21,212,099 IFNWP18, IFNA10, 1 more genes
    nsv6637750copy number variation1nstd102humanUncertain significance GRCh37 chr9: 20,659,492-22,347,440 , GRCh38.p12 chr9: 20,659,493-22,347,441 CDKN2B, IFNA10, 46 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
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