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Items: 1 to 20 of 162

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5969626insertion1nstd209human GRCh38 chr19: 36,044,426-36,044,426 , GRCh37.p13 chr19: 36,535,328-36,535,328 THAP8, LOC101927572
    nsv5706040mobile element insertion2nstd211human GRCh38 chr19: 36,044,439-36,044,439 , GRCh37.p13 chr19: 36,535,341-36,535,341 THAP8, LOC101927572
    nsv5654727insertion1nstd207human GRCh38 chr19: 36,048,556-36,048,556 , GRCh37.p13 chr19: 36,539,458-36,539,458 THAP8, RNY5P10, 1 more genes
    nsv5648014insertion1nstd207human GRCh38 chr19: 36,044,426-36,044,426 , GRCh37.p13 chr19: 36,535,328-36,535,328 THAP8, LOC101927572
    nsv5531520copy number variation1nstd206human GRCh38 chr19: 36,029,513-36,044,516 , GRCh37.p13 chr19: 36,520,415-36,535,418 CLIP3, THAP8, 1 more genes
    nsv5528024copy number variation1nstd206human GRCh38 chr19: 36,018,020-36,084,516 , GRCh37.p13 chr19: 36,508,922-36,575,418 WDR62, RNY5P10, 3 more genes
    nsv5424881mobile element insertion1nstd206human GRCh38 chr19: 36,044,426-36,044,426 , GRCh37.p13 chr19: 36,535,328-36,535,328 LOC101927572, THAP8
    nsv5289021copy number variation1nstd204human GRCh38.p13 chr19: 36,002,801-36,145,200 , GRCh37.p13 chr19: 36,493,703-36,636,102 LOC101927572, THAP8, 10 more genes
    nsv5281358copy number variation1nstd204human GRCh38.p13 chr19: 36,024,201-36,072,100 , GRCh37.p13 chr19: 36,515,103-36,563,002 CLIP3, RNY5P10, 3 more genes
    nsv5173871mobile element insertion1nstd203human GRCh38 chr19: 36,044,424-36,044,439 , GRCh37.p13 chr19: 36,535,326-36,535,341 LOC101927572, THAP8
    nsv5169348mobile element insertion1nstd203human GRCh38 chr19: 36,044,433-36,044,439 , GRCh37.p13 chr19: 36,535,335-36,535,341 LOC101927572, THAP8
    nsv5163132mobile element insertion1nstd203human GRCh38 chr19: 36,044,426-36,044,439 , GRCh37.p13 chr19: 36,535,328-36,535,341 LOC101927572, THAP8
    nsv5027724copy number variation1nstd200human GRCh38 chr19: 36,043,774-36,055,812 , GRCh37.p13 chr19: 36,534,676-36,546,714 WDR62, RNY5P10, 2 more genes
    nsv5024570copy number variation1nstd200human GRCh38 chr19: 35,722,805-36,225,611 , GRCh37.p13 chr19: 36,213,707-36,716,513 LOC105372385, ALKBH6, 34 more genes
    nsv4865133copy number variation1nstd200human GRCh37 chr19: 36,213,707-36,716,513 , GRCh38.p12 chr19: 35,722,805-36,225,611 KMT2B, PSENEN, 34 more genes
    nsv4764199insertion1nstd199human GRCh37 chr19: 36,535,334-36,535,334 , GRCh38.p12 chr19: 36,044,432-36,044,432 THAP8, LOC101927572
    nsv4718529mobile element insertion2nstd186human GRCh37 chr19: 36,535,328-36,535,328 , GRCh38.p12 chr19: 36,044,426-36,044,426 THAP8, LOC101927572
    nsv4689647mobile element insertion1nstd186human GRCh37 chr19: 36,535,341-36,535,341 , GRCh38.p12 chr19: 36,044,439-36,044,439 THAP8, LOC101927572
    nsv4535651copy number variation1nstd166human GRCh37.p13 chr19: 36,540,982-36,541,171 , GRCh38.p12 chr19: 36,050,080-36,050,269 THAP8, LOC101927572
    nsv4515918mobile element insertion1nstd166human GRCh37.p13 chr19: 36,535,328-36,535,328 , GRCh38.p12 chr19: 36,044,426-36,044,426 LOC101927572, THAP8
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