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Items: 1 to 20 of 196

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112754copy number variation1nstd102humanPathogenic GRCh37 chr4: 131,303,317-168,722,402 , GRCh38.p12 chr4: 130,382,162-167,801,251 MIR3139, CLGN, 407 more genes
    nsv5947940insertion1nstd209human GRCh38 chr4: 143,205,943-143,205,943 , GRCh37.p13 chr4: 144,127,096-144,127,096 USP38
    nsv5728236mobile element insertion1nstd211human GRCh38 chr4: 143,224,277-143,224,277 , GRCh37.p13 chr4: 144,145,430-144,145,430 USP38
    nsv5678530mobile element insertion2nstd211human GRCh38 chr4: 143,205,962-143,205,962 , GRCh37.p13 chr4: 144,127,115-144,127,115 USP38
    nsv5617268insertion1nstd207human GRCh38 chr4: 143,184,836-143,184,836 , GRCh37.p13 chr4: 144,105,989-144,105,989 USP38-DT, USP38
    nsv5562145sequence alteration1nstd206human GRCh38 chr4: 74,717,205-184,730,527 , GRCh37.p13 chr4: 75,689,880-185,651,681 , ASS1P8, 1307 more genes
    nsv5558407mobile element insertion1nstd206human GRCh38 chr4: 143,224,277-143,224,289 , GRCh37.p13 chr4: 144,145,430-144,145,442 USP38
    nsv5558253sequence alteration1nstd206human GRCh38 chr4: 120,373,769-143,797,136 , GRCh37.p13 chr4: 121,294,924-144,718,289 , IL15, 218 more genes
    nsv5400156mobile element insertion1nstd206human GRCh38 chr4: 143,205,962-143,206,013 , GRCh37.p13 chr4: 144,127,115-144,127,166 USP38
    nsv5377665translocation1nstd200human GRCh38 chr17: 75,130,664-75,130,664 , GRCh38 chr4: 143,217,245-143,217,245 , GRCh37.p13 chr17: 73,126,759-73,126,759 , GRCh37.p13 chr4: 144,138,398-144,138,398 NT5C, ARMC7, 2 more genes
    nsv5179075mobile element insertion1nstd203human GRCh38 chr4: 143,224,277-143,224,289 , GRCh37.p13 chr4: 144,145,430-144,145,442 USP38
    nsv5099628mobile element insertion1nstd203human GRCh38 chr4: 143,189,533-143,189,544 , GRCh37.p13 chr4: 144,110,686-144,110,697 USP38
    nsv5099341mobile element insertion1nstd203human GRCh38 chr4: 143,205,949-143,205,962 , GRCh37.p13 chr4: 144,127,102-144,127,115 USP38
    nsv5099276mobile element insertion1nstd203human GRCh38 chr4: 143,189,446-143,189,462 , GRCh37.p13 chr4: 144,110,599-144,110,615 USP38
    nsv5097516mobile element insertion1nstd203human GRCh38 chr4: 143,205,947-143,205,962 , GRCh37.p13 chr4: 144,127,100-144,127,115 USP38
    nsv5095326mobile element insertion1nstd203human GRCh38 chr4: 143,205,945-143,205,961 , GRCh37.p13 chr4: 144,127,098-144,127,114 USP38
    nsv5093728mobile element insertion1nstd203human GRCh38 chr4: 143,205,942-143,205,962 , GRCh37.p13 chr4: 144,127,095-144,127,115 USP38
    nsv5087768mobile element insertion1nstd203human GRCh38 chr4: 143,205,946-143,205,962 , GRCh37.p13 chr4: 144,127,099-144,127,115 USP38
    nsv5085551mobile element insertion1nstd203human GRCh38 chr4: 143,205,953-143,205,962 , GRCh37.p13 chr4: 144,127,106-144,127,115 USP38
    nsv5085315mobile element insertion1nstd203human GRCh38 chr4: 143,205,948-143,205,962 , GRCh37.p13 chr4: 144,127,101-144,127,115 USP38
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