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Items: 1 to 20 of 273

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5979328inversion1nstd209human GRCh38 chr19: 32,019,307-33,218,671 , GRCh37.p13 chr19: 32,510,213-33,709,577 , LRP3, 28 more genes
    nsv5972491insertion1nstd209human GRCh38 chr19: 32,445,440-32,445,440 , GRCh37.p13 chr19: 32,936,346-32,936,346 DPY19L3
    nsv5936146copy number variation1nstd209human GRCh38 chr19: 32,446,697-32,448,563 , GRCh37.p13 chr19: 32,937,603-32,939,469 DPY19L3
    nsv5877573copy number variation2nstd209human GRCh38 chr19: 32,446,926-32,447,965 , GRCh37.p13 chr19: 32,937,832-32,938,871 DPY19L3
    nsv5870989copy number variation1nstd209human GRCh38 chr19: 32,446,676-32,449,165 , GRCh37.p13 chr19: 32,937,582-32,940,071 DPY19L3
    nsv5719182mobile element insertion1nstd211human GRCh38 chr19: 32,414,427-32,414,427 , GRCh37.p13 chr19: 32,905,333-32,905,333 DPY19L3
    nsv5525971copy number variation1nstd206human GRCh38 chr19: 32,434,189-32,434,397 , GRCh37.p13 chr19: 32,925,095-32,925,303 DPY19L3
    nsv5199654mobile element insertion1nstd203human GRCh38 chr19: 32,483,716-32,483,722 , GRCh37.p13 chr19: 32,974,622-32,974,628 DPY19L3
    nsv5024519copy number variation1nstd200human GRCh38 chr19: 28,925,173-32,768,971 , GRCh37.p13 chr19: 29,416,080-33,259,877 , LOC105372355, 53 more genes
    nsv5020324copy number variation1nstd200human GRCh38 chr19: 32,424,302-32,431,335 , GRCh37.p13 chr19: 32,915,208-32,922,241 DPY19L3
    nsv5020323copy number variation1nstd200human GRCh38 chr19: 32,404,026-32,404,097 , GRCh37.p13 chr19: 32,894,932-32,895,003 DPY19L3, DPY19L3-DT
    nsv4715921copy number variation1nstd195human GRCh37 chr19: 32,145,451-33,022,201 , GRCh38.p12 chr19: 31,654,545-32,531,295 , DPY19L3, 12 more genes
    nsv4712385copy number variation1nstd195human GRCh37 chr19: 32,145,451-33,078,501 , GRCh38.p12 chr19: 31,654,545-32,587,595 , DPY19L3-DT, 13 more genes
    nsv4633430copy number variation1nstd183human GRCh37 chr19: 32,909,493-32,911,209 , GRCh38.p12 chr19: 32,418,587-32,420,303 DPY19L3
    nsv4622003copy number variation1nstd183human GRCh37 chr19: 32,902,406-32,911,224 , GRCh38.p12 chr19: 32,411,500-32,420,318 DPY19L3
    nsv4559706mobile element insertion1nstd166human GRCh37.p13 chr19: 32,974,622-32,974,622 , GRCh38.p12 chr19: 32,483,716-32,483,716 DPY19L3
    nsv4514194mobile element insertion1nstd166human GRCh37.p13 chr19: 32,964,200-32,964,200 , GRCh38.p12 chr19: 32,473,294-32,473,294 DPY19L3
    nsv4509956mobile element insertion1nstd166human GRCh37.p13 chr19: 32,973,601-32,973,601 , GRCh38.p12 chr19: 32,482,695-32,482,695 DPY19L3
    nsv4502072mobile element insertion1nstd166human GRCh37.p13 chr19: 32,975,729-32,975,729 , GRCh38.p12 chr19: 32,484,823-32,484,823 DPY19L3
    nsv4457372copy number variation1nstd102humanPathogenic GRCh37 chr19: 28,271,106-49,213,832 , GRCh38.p12 chr19: 27,780,198-48,710,575 ZNF461, LOC101927572, 735 more genes
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