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Items: 1 to 20 of 287

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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
    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
    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
    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
    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
    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
    nsv6634409copy number variation1nstd102humanLikely pathogenic GRCh37 chr9: 1-40,036,525 , GRCh38.p12 chr9: 10,001-39,445,729 ACO1, PLIN2, 594 more genes
    nsv6633714copy number variation1nstd224human GRCh37 chr9: 21,166,236-21,202,158 , GRCh38.p12 chr9: 21,166,237-21,202,159 IFNA4, IFNA7, 3 more genes
    nsv6633713copy number variation1nstd224human GRCh37 chr9: 21,157,373-21,217,018 , GRCh38.p12 chr9: 21,157,374-21,217,019 IFNA4, IFNA7, 6 more genes
    nsv6633712copy number variation1nstd224human GRCh37 chr9: 21,121,917-21,278,750 , GRCh38.p12 chr9: 21,121,918-21,278,751 IFNA7, IFNA22P, 12 more genes
    nsv6633251copy number variation1nstd224human GRCh37 chr9: 20,976,421-21,415,687 , GRCh38.p12 chr9: 20,976,422-21,415,688 IFNA5, IFNA16, 27 more genes
    nsv6633190copy number variation1nstd224human GRCh37 chr9: 20,981,542-21,217,018 , GRCh38.p12 chr9: 20,981,543-21,217,019 IFNA7, IFNWP4, 13 more genes
    nsv6562498inversion1nstd223human GRCh38 chr9: 20,655,689-27,693,631 , GRCh37.p13 chr9: 20,655,688-27,693,629 IFNA7, IFNW1, 92 more genes
    nsv6435256copy number variation1nstd223human GRCh38 chr9: 21,181,008-21,228,183 , GRCh37.p13 chr9: 21,181,007-21,228,182 IFNA4, IFNA7, 5 more genes
    nsv6430997copy number variation1nstd223human GRCh38 chr9: 21,038,118-21,284,702 , GRCh37.p13 chr9: 21,038,117-21,284,701 IFNWP4, IFNA10, 16 more genes
    nsv6420362copy number variation1nstd223human GRCh38 chr9: 21,188,001-21,190,400 , GRCh37.p13 chr9: 21,188,000-21,190,399 IFNWP9, IFNA4
    nsv6419725copy number variation1nstd223human GRCh38 chr9: 21,166,988-21,202,510 , GRCh37.p13 chr9: 21,166,987-21,202,509 IFNA4, IFNA21, 3 more genes
    nsv6418682copy number variation1nstd223human GRCh38 chr9: 21,178,885-21,191,042 , GRCh37.p13 chr9: 21,178,884-21,191,041 IFNWP9, IFNA4, 1 more genes
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