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Items: 1 to 20 of 165

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7076785inversion1nstd229human GRCh38 chr20: 36,001,722-37,069,571 , GRCh37.p13 chr20: 34,589,644-35,697,974 RPS3AP3, EPB41L1-AS1, 22 more genes
    nsv7059005inversion1nstd229human GRCh38 chr20: 36,250,254-36,253,727 , GRCh37.p13 chr20: 34,838,176-34,841,649 AAR2
    nsv7035007copy number variation1nstd229human GRCh38 chr20: 36,254,457-36,254,532 , GRCh37.p13 chr20: 34,842,379-34,842,454 AAR2
    nsv7028529copy number variation1nstd229human GRCh38 chr20: 36,256,702-36,266,581 , GRCh37.p13 chr20: 34,844,624-34,854,503 AAR2
    nsv7028457copy number variation1nstd229human GRCh38 chr20: 36,246,191-36,249,303 , GRCh37.p13 chr20: 34,834,113-34,837,225 AAR2
    nsv7021198copy number variation1nstd229human GRCh38 chr20: 33,145,032-41,995,765 , GRCh37.p13 chr20: 31,732,838-40,624,405 PXMP4, RPL12P11, 199 more genes
    nsv6637546copy number variation1nstd102humanLikely pathogenic GRCh37 chr20: 29,652,122-35,603,726 , GRCh38.p12 chr20: 30,417,446-36,975,323 AHCY, ASIP, 195 more genes
    nsv6599442inversion1nstd223human GRCh38 chr20: 36,247,696-36,248,345 , GRCh37.p13 chr20: 34,835,618-34,836,267 AAR2
    nsv6531541copy number variation1nstd223human GRCh38 chr20: 36,250,131-36,250,577 , GRCh37.p13 chr20: 34,838,053-34,838,499 AAR2
    nsv6526683copy number variation1nstd223human GRCh38 chr20: 36,256,702-36,266,576 , GRCh37.p13 chr20: 34,844,624-34,854,498 AAR2
    nsv6516000copy number variation1nstd223human GRCh38 chr20: 36,246,190-36,249,301 , GRCh37.p13 chr20: 34,834,112-34,837,223 AAR2
    nsv6281042copy number variation1nstd214human GRCh38 chr20: 36,254,444-36,254,517 , GRCh37.p13 chr20: 34,842,366-34,842,439 AAR2
    nsv6134023copy number variation1nstd213human GRCh37 chr20: 34,270,000-35,840,001 , GRCh38.p12 chr20: 35,682,078-37,211,598 RBL1, AAR2, 35 more genes
    nsv6105354insertion1nstd212human GRCh38 chr20: 36,236,209-36,236,209 , GRCh37.p13 chr20: 34,824,131-34,824,131 LOC105372602, AAR2
    nsv5959195copy number variation1nstd209human GRCh38 chr20: 36,254,444-36,254,517 , GRCh37.p13 chr20: 34,842,366-34,842,439 AAR2
    nsv5527576copy number variation1nstd206human GRCh38 chr20: 36,256,702-36,266,576 , GRCh37.p13 chr20: 34,844,624-34,854,498 AAR2
    nsv5366096translocation1nstd200human GRCh38 chr20: 36,253,581-36,253,581 , GRCh38 chr20: 36,253,732-36,253,732 , GRCh37.p13 chr20: 34,841,503-34,841,503 , GRCh37.p13 chr20: 34,841,654-34,841,654 AAR2
    nsv5028468copy number variation1nstd200human GRCh38 chr20: 36,256,702-36,266,576 , GRCh37.p13 chr20: 34,844,624-34,854,498 AAR2
    nsv5028467copy number variation1nstd200human GRCh38 chr20: 36,250,253-36,253,731 , GRCh37.p13 chr20: 34,838,175-34,841,653 AAR2
    nsv5022343copy number variation1nstd200human GRCh38 chr20: 32,602,560-45,347,064 , GRCh37.p13 chr20: 31,190,362-43,975,704 , SNHG11, 286 more genes
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