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Items: 1 to 20 of 269

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7139695copy number variation1nstd232human GRCh37.p13 chr3: 57,161,249-57,161,310 , GRCh38.p12 chr3: 57,127,221-57,127,282 IL17RD
    nsv7097210copy number variation1nstd102humanUncertain significance GRCh37 chr3: 57,130,421-58,520,833 , GRCh38.p12 chr3: 57,096,393-58,535,106 LOC107984079, SLMAP, 37 more genes
    nsv7097209copy number variation1nstd102humanUncertain significance GRCh37 chr3: 57,130,421-57,303,715 , GRCh38.p12 chr3: 57,096,393-57,269,687 APPL1, LOC105377102, 5 more genes
    nsv7051968inversion1nstd229human GRCh38 chr3: 56,944,702-65,952,705 , GRCh37.p13 chr3: 56,978,730-65,938,380 ILF2P1, ARHGEF3-AS1, 115 more genes
    nsv7038236inversion1nstd229human GRCh38 chr3: 56,950,550-57,362,669 , GRCh37.p13 chr3: 56,984,578-57,369,477 SPATA12, APPL1, 9 more genes
    nsv6716608copy number variation1nstd229human GRCh38 chr3: 57,104,523-57,111,230 , GRCh37.p13 chr3: 57,138,551-57,145,258 IL17RD
    nsv6712344copy number variation1nstd229human GRCh38 chr3: 57,107,149-57,108,951 , GRCh37.p13 chr3: 57,141,177-57,142,979 IL17RD
    nsv6711553copy number variation1nstd229human GRCh38 chr3: 56,820,001-57,251,300 , GRCh37.p13 chr3: 56,854,029-57,285,328 HESX1, ARHGEF3-AS1, 6 more genes
    nsv6710941copy number variation1nstd229human GRCh38 chr3: 57,127,000-57,132,962 , GRCh37.p13 chr3: 57,161,028-57,166,990 IL17RD, RPL19P2
    nsv6708426copy number variation1nstd229human GRCh38 chr3: 57,153,042-57,153,247 , GRCh37.p13 chr3: 57,187,070-57,187,275 IL17RD, LOC105377101
    nsv6701927copy number variation1nstd229human GRCh38 chr3: 56,896,049-57,237,863 , GRCh37.p13 chr3: 56,930,077-57,271,891 LOC105377101, RPL19P2, 6 more genes
    nsv6699589copy number variation1nstd229human GRCh38 chr3: 57,084,141-57,097,801 , GRCh37.p13 chr3: 57,118,169-57,131,829 IL17RD
    nsv6698314copy number variation1nstd229human GRCh38 chr3: 57,170,340-57,172,669 , GRCh37.p13 chr3: 57,204,368-57,206,697 IL17RD
    nsv6698127copy number variation1nstd229human GRCh38 chr3: 57,088,206-57,091,416 , GRCh37.p13 chr3: 57,122,234-57,125,444 IL17RD
    nsv6542823inversion1nstd223human GRCh38 chr3: 57,113,378-57,113,915 , GRCh37.p13 chr3: 57,147,406-57,147,943 IL17RD
    nsv6375341copy number variation1nstd223human GRCh38 chr3: 57,170,339-57,172,668 , GRCh37.p13 chr3: 57,204,367-57,206,696 IL17RD
    nsv6374422copy number variation1nstd223human GRCh38 chr3: 57,162,821-57,163,863 , GRCh37.p13 chr3: 57,196,849-57,197,891 IL17RD
    nsv6363440copy number variation1nstd223human GRCh38 chr3: 57,155,200-57,157,488 , GRCh37.p13 chr3: 57,189,228-57,191,516 IL17RD
    nsv6362917copy number variation1nstd223human GRCh38 chr3: 57,129,701-57,131,400 , GRCh37.p13 chr3: 57,163,729-57,165,428 IL17RD
    nsv6357004copy number variation1nstd223human GRCh38 chr3: 57,088,203-57,091,414 , GRCh37.p13 chr3: 57,122,231-57,125,442 IL17RD
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