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Items: 1 to 20 of 190

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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
    nsv7028662copy number variation1nstd229human GRCh38 chr20: 36,746,479-36,832,051 , GRCh37.p13 chr20: 35,374,882-35,460,454 NDRG3, DSN1, 1 more genes
    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
    nsv7018629copy number variation1nstd229human GRCh38 chr20: 36,683,202-36,775,933 , GRCh37.p13 chr20: 35,311,605-35,404,336 DSN1, MTCL2, 1 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
    nsv6599176inversion1nstd223human GRCh38 chr20: 36,751,114-36,753,848 , GRCh37.p13 chr20: 35,379,517-35,382,251 DSN1
    nsv6598398inversion1nstd223human GRCh38 chr20: 36,752,513-36,752,641 , GRCh37.p13 chr20: 35,380,916-35,381,044 DSN1
    nsv6597484inversion1nstd223human GRCh38 chr20: 36,759,684-36,760,192 , GRCh37.p13 chr20: 35,388,087-35,388,595 DSN1
    nsv6533720copy number variation1nstd223human GRCh38 chr20: 36,757,304-36,760,192 , GRCh37.p13 chr20: 35,385,707-35,388,595 DSN1
    nsv6530948copy number variation1nstd223human GRCh38 chr20: 36,763,719-36,766,499 , GRCh37.p13 chr20: 35,392,122-35,394,902 DSN1
    nsv6521229copy number variation1nstd223human GRCh38 chr20: 36,760,865-36,763,885 , GRCh37.p13 chr20: 35,389,268-35,392,288 DSN1
    nsv6291474copy number variation1nstd102humanUncertain significance GRCh37 chr20: 35,335,325-35,606,892 , GRCh38.p12 chr20: 36,706,922-36,978,489 TLDC2, SAMHD1, 4 more genes
    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
    nsv6109306insertion1nstd212human GRCh38 chr20: 36,750,590-36,750,590 , GRCh37.p13 chr20: 35,378,993-35,378,993 DSN1
    nsv5724574mobile element insertion2nstd211human GRCh38 chr20: 36,756,707-36,756,707 , GRCh37.p13 chr20: 35,385,110-35,385,110 DSN1
    nsv5706364mobile element insertion2nstd211human GRCh38 chr20: 36,756,696-36,756,696 , GRCh37.p13 chr20: 35,385,099-35,385,099 DSN1
    nsv5670540insertion1nstd207human GRCh38 chr20: 36,756,696-36,756,696 , GRCh37.p13 chr20: 35,385,099-35,385,099 DSN1
    nsv5428600mobile element insertion1nstd206human GRCh38 chr20: 36,756,707-36,756,747 , GRCh37.p13 chr20: 35,385,110-35,385,150 DSN1
    nsv5327073copy number variation1nstd204human GRCh38.p13 chr20: 36,689,836-36,821,542 , GRCh37.p13 chr20: 35,318,239-35,449,945 NDRG3, DSN1, 1 more genes
    nsv5296148copy number variation1nstd204human GRCh38.p13 chr20: 36,690,201-36,821,100 , GRCh37.p13 chr20: 35,318,604-35,449,503 NDRG3, DSN1, 1 more genes
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