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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5976901inversion1nstd209human GRCh38 chr19: 20,618,550-20,701,042 , GRCh37.p13 chr19: 20,801,356-20,845,946 , GRCh37.p13 chr19|NW_003571053.2: 535,803-580,393 ZNF626, LOC100533638, 2 more genes
    nsv5946439copy number variation1nstd209human GRCh37.p13 chr19|NW_003571053.2: 321,729-556,649 , GRCh38 chr19: 20,404,476-20,639,396 , GRCh37.p13 chr19: 20,515,285-20,822,202 ZNF626, ZNF826P, 7 more genes
    nsv5886030copy number variation1nstd209human GRCh38 chr19: 20,640,276-20,665,502 , GRCh37.p13 chr19: 20,823,082-20,845,946 , GRCh37.p13 chr19|NW_003571053.2: 557,529-580,393 LOC105372319, ZNF626
    nsv5877171copy number variation1nstd209human GRCh38 chr19: 20,633,628-20,635,227 , GRCh37.p13 chr19|NW_003571053.2: 550,881-552,480 , GRCh37.p13 chr19: 20,816,434-20,818,033 ZNF626
    nsv5876734copy number variation1nstd209human GRCh38 chr19: 20,619,234-20,636,102 , GRCh37.p13 chr19: 20,802,040-20,818,885 , GRCh37.p13 chr19|NW_003571053.2: 536,487-553,355 ZNF626
    nsv5715708mobile element insertion1nstd211human GRCh38 chr19: 20,645,884-20,645,884 , GRCh37.p13 chr19: 20,828,690-20,828,690 , GRCh37.p13 chr19|NW_003571053.2: 563,137-563,137 ZNF626
    nsv5603190copy number variation1nstd207human GRCh37.p13 chr19|NW_003571053.2: 542,413-542,496 , GRCh38 chr19: 20,625,160-20,625,243 , GRCh37.p13 chr19: 20,807,966-20,808,049 ZNF626
    nsv5599111copy number variation1nstd207human GRCh38 chr19: 20,624,327-20,624,493 , GRCh37.p13 chr19: 20,807,133-20,807,299 , GRCh37.p13 chr19|NW_003571053.2: 541,580-541,746 ZNF626
    nsv5558864sequence alteration1nstd206human GRCh37.p13 chr19|NW_003571053.2: 535,802-580,393 , GRCh38 chr19: 20,618,549-20,701,043 , GRCh37.p13 chr19: 20,801,355-20,845,946 ZNF626, LOC100533638, 2 more genes
    nsv5556528sequence alteration1nstd206human GRCh37.p13 chr19|NW_003571053.2: 354,141-580,393 , GRCh38 chr19: 20,436,888-20,771,101 , GRCh37.p13 chr19: 20,619,694-20,845,946 ZNF626, BNIP3P23, 8 more genes
    nsv5554087sequence alteration1nstd206human GRCh38 chr19: 20,570,716-20,771,204 , GRCh37.p13 chr19: 20,845,947-20,954,010 ZNF626, VN1R78P, 5 more genes
    nsv5533646copy number variation1nstd206human GRCh38 chr19: 20,645,884-20,812,895 , GRCh37.p13 chr19: 20,845,947-20,995,701 ZNF66, ZNF626, 4 more genes
    nsv5532523copy number variation1nstd206human GRCh38 chr19: 20,045,607-20,884,415 , GRCh37.p13 chr19|NW_003571053.2: 1-580,393 , GRCh37.p13 chr19: 20,156,416-21,067,221 , LOC100419841, 37 more genes
    nsv5532267copy number variation1nstd206human GRCh38 chr19: 20,624,360-20,624,947 , GRCh37.p13 chr19|NW_003571053.2: 541,613-542,200 , GRCh37.p13 chr19: 20,807,166-20,807,753 ZNF626
    nsv5527568copy number variation1nstd206human GRCh37.p13 chr19|NW_003571053.2: 384,356-580,393 , GRCh38 chr19: 20,467,103-20,678,966 , GRCh37.p13 chr19: 20,649,909-20,845,946 ZNF626, ZNF737, 4 more genes
    nsv5389566copy number variation1nstd186human GRCh37 chr19: 20,807,205-20,807,411 , GRCh38.p12 chr19: 20,624,399-20,624,605 ZNF626
    nsv5375348translocation1nstd200human GRCh38 chr19: 20,619,252-20,619,252 , GRCh38 chr19: 20,700,180-20,700,180 , GRCh37.p13 chr19: 20,882,986-20,882,986 , GRCh37.p13 chr19|NW_003571053.2: 536,505-536,505 , GRCh37.p13 chr19: 20,802,058-20,802,058 ZNF626
    nsv5330550translocation1nstd200human GRCh37 chr19: 20,802,059-20,802,059 , GRCh37 chr19: 20,882,985-20,882,985 , GRCh38.p12 chr19: 20,619,253-20,619,253 , GRCh38.p12 chr19: 20,700,179-20,700,179 , GRCh38.p12 chr19|NW_003315962.1: 37,039-37,039 ZNF626
    nsv5329343copy number variation1nstd204human GRCh38.p13 chr19: 20,621,064-20,621,344 , GRCh37.p13 chr19: 20,803,870-20,804,150 , GRCh37.p13 chr19|NW_003571053.2: 538,317-538,597 ZNF626
    nsv5329016copy number variation1nstd204human GRCh38.p13 chr19: 20,624,355-20,624,632 , GRCh37.p13 chr19|NW_003571053.2: 541,608-541,885 , GRCh37.p13 chr19: 20,807,161-20,807,438 ZNF626
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