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Items: 1 to 20 of 247

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7145258insertion1nstd232human GRCh37.p13 chr20: 35,521,472-35,521,472 , GRCh38.p12 chr20: 36,893,069-36,893,069 SAMHD1, TLDC2
    nsv7096075copy number variation1nstd102humanUncertain significance GRCh37 chr20: 35,521,335-35,526,967 , GRCh38.p12 chr20: 36,892,932-36,898,564 TLDC2, SAMHD1
    nsv7095893copy number variation1nstd102humanUncertain significance GRCh37 chr20: 35,521,335-35,540,975 , GRCh38.p12 chr20: 36,892,932-36,912,572 SAMHD1, TLDC2
    nsv7076785inversion1nstd229human GRCh38 chr20: 36,001,722-37,069,571 , GRCh37.p13 chr20: 34,589,644-35,697,974 RPS3AP3, EPB41L1-AS1, 22 more genes
    nsv7036526copy number variation1nstd229human GRCh38 chr20: 36,880,772-36,884,367 , GRCh37.p13 chr20: 35,509,175-35,512,770 TLDC2
    nsv7033994copy number variation1nstd229human GRCh38 chr20: 36,894,401-36,896,200 , GRCh37.p13 chr20: 35,522,804-35,524,603 TLDC2, SAMHD1
    nsv7025734copy number variation1nstd229human GRCh38 chr20: 36,868,646-36,871,441 , GRCh37.p13 chr20: 35,497,049-35,499,844 TLDC2, RN7SL156P
    nsv7024754copy number variation1nstd229human GRCh38 chr20: 36,878,345-36,879,606 , GRCh37.p13 chr20: 35,506,748-35,508,009 TLDC2
    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
    nsv7020177copy number variation1nstd229human GRCh38 chr20: 36,801,699-36,878,314 , GRCh37.p13 chr20: 35,430,102-35,506,717 MTCL2, TLDC2, 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
    nsv6596833inversion1nstd223human GRCh38 chr20: 36,870,521-36,871,428 , GRCh37.p13 chr20: 35,498,924-35,499,831 TLDC2, RN7SL156P
    nsv6534892copy number variation1nstd223human GRCh38 chr20: 36,878,307-36,879,567 , GRCh37.p13 chr20: 35,506,710-35,507,970 TLDC2
    nsv6534272copy number variation1nstd223human GRCh38 chr20: 36,888,539-36,893,416 , GRCh37.p13 chr20: 35,516,942-35,521,819 SAMHD1, TLDC2
    nsv6533774copy number variation1nstd223human GRCh38 chr20: 36,852,998-36,913,501 , GRCh37.p13 chr20: 35,481,401-35,541,904 MTCL2, TLDC2, 2 more genes
    nsv6533399copy number variation1nstd223human GRCh38 chr20: 36,894,399-36,896,140 , GRCh37.p13 chr20: 35,522,802-35,524,543 SAMHD1, TLDC2
    nsv6531043copy number variation1nstd223human GRCh38 chr20: 36,894,465-36,901,704 , GRCh37.p13 chr20: 35,522,868-35,530,107 SAMHD1, TLDC2
    nsv6530755copy number variation1nstd223human GRCh38 chr20: 36,876,519-36,877,079 , GRCh37.p13 chr20: 35,504,922-35,505,482 TLDC2
    nsv6526715copy number variation1nstd223human GRCh38 chr20: 36,894,501-36,896,300 , GRCh37.p13 chr20: 35,522,904-35,524,703 SAMHD1, TLDC2
    nsv6524110copy number variation1nstd223human GRCh38 chr20: 36,874,618-36,940,112 , GRCh37.p13 chr20: 35,503,021-35,568,515 SAMHD1, TLDC2
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