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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6873486copy number variation1nstd229human GRCh38 chr9: 70,279,292-70,279,868 , GRCh37.p13 chr9: 72,894,208-72,894,784 SMC5
    nsv6873470copy number variation1nstd229human GRCh38 chr9: 70,225,601-70,561,100 , GRCh37.p13 chr9: 72,840,517-73,176,016 MAMDC2, KLF9, 5 more genes
    nsv6871886copy number variation1nstd229human GRCh38 chr9: 70,287,401-70,297,000 , GRCh37.p13 chr9: 72,902,317-72,911,916 SMC5
    nsv6867906copy number variation1nstd229human GRCh38 chr9: 70,327,675-70,330,544 , GRCh37.p13 chr9: 72,942,591-72,945,460 SMC5
    nsv6864082copy number variation1nstd229human GRCh38 chr9: 70,348,475-70,349,280 , GRCh37.p13 chr9: 72,963,391-72,964,196 SMC5
    nsv6862944copy number variation1nstd229human GRCh38 chr9: 70,128,037-70,524,907 , GRCh37.p13 chr9: 72,742,953-73,139,823 LOC105376079, RPL24P8, 7 more genes
    nsv6860782copy number variation1nstd229human GRCh38 chr9: 70,318,749-70,739,208 , GRCh37.p13 chr9: 72,933,665-73,354,124 KLF9, KLF9-DT, 6 more genes
    nsv6858556copy number variation1nstd229human GRCh38 chr9: 69,469,082-70,263,273 , GRCh37.p13 chr9: 72,083,998-72,878,189 RNU2-5P, APBA1, 10 more genes
    nsv6637502copy number variation1nstd102humanUncertain significance GRCh37 chr9: 70,966,262-76,901,382 , GRCh38.p12 chr9: 68,351,346-74,286,466 RPS20P24, MAMDC2-AS1, 77 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
    nsv6570414inversion1nstd223human GRCh38 chr9: 70,307,811-70,308,296 , GRCh37.p13 chr9: 72,922,727-72,923,212 SMC5
    nsv6567192inversion1nstd223human GRCh38 chr9: 70,307,248-70,308,007 , GRCh37.p13 chr9: 72,922,164-72,922,923 SMC5
    nsv6451325copy number variation1nstd223human GRCh38 chr9: 70,257,401-70,262,200 , GRCh37.p13 chr9: 72,872,317-72,877,116 SMC5-DT, SMC5
    nsv6451041copy number variation1nstd223human GRCh38 chr9: 70,281,401-70,282,600 , GRCh37.p13 chr9: 72,896,317-72,897,516 SMC5
    nsv6448822copy number variation1nstd223human GRCh38 chr9: 70,287,393-70,296,947 , GRCh37.p13 chr9: 72,902,309-72,911,863 SMC5
    nsv6445447copy number variation1nstd223human GRCh38 chr9: 70,239,607-70,312,840 , GRCh37.p13 chr9: 72,854,523-72,927,756 SMC5-DT, SMC5
    nsv6444158copy number variation1nstd223human GRCh38 chr9: 70,277,301-70,278,400 , GRCh37.p13 chr9: 72,892,217-72,893,316 SMC5
    nsv6442378copy number variation1nstd223human GRCh38 chr9: 70,291,429-70,291,864 , GRCh37.p13 chr9: 72,906,345-72,906,780 SMC5
    nsv6442231copy number variation1nstd223human GRCh38 chr9: 70,297,959-70,298,667 , GRCh37.p13 chr9: 72,912,875-72,913,583 SMC5
    nsv6437564copy number variation1nstd223human GRCh38 chr9: 70,299,142-70,299,771 , GRCh37.p13 chr9: 72,914,058-72,914,687 SMC5
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