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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112763copy number variation1nstd102humanPathogenic GRCh37 chr12: 189,145-7,730,395 , GRCh38.p12 chr12: 79,979-7,577,799 GALNT8, LINC02371, 197 more genes
    nsv5980019insertion1nstd209human GRCh38 chr12: 4,734,671-4,734,671 , GRCh37.p13 chr12: 4,843,837-4,843,837 GALNT8
    nsv5921920copy number variation1nstd209human GRCh38 chr12: 3,058,695-6,171,259 , GRCh37.p13 chr12: 3,167,861-6,280,425 , LOC105369623, 54 more genes
    nsv5917227copy number variation1nstd209human GRCh38 chr12: 4,732,055-4,732,130 , GRCh37.p13 chr12: 4,841,221-4,841,296 GALNT8
    nsv5911382copy number variation1nstd209human GRCh38 chr12: 4,750,248-4,764,109 , GRCh37.p13 chr12: 4,859,414-4,873,275 GALNT8
    nsv5862961copy number variation1nstd209human GRCh38 chr12: 4,765,058-4,768,081 , GRCh37.p13 chr12: 4,874,224-4,877,247 GALNT8
    nsv5862918copy number variation1nstd209human GRCh38 chr12: 4,765,158-4,767,481 , GRCh37.p13 chr12: 4,874,324-4,876,647 GALNT8
    nsv5862368copy number variation1nstd209human GRCh38 chr12: 4,750,174-4,755,480 , GRCh37.p13 chr12: 4,859,340-4,864,646 GALNT8
    nsv5862117copy number variation1nstd209human GRCh38 chr12: 4,754,881-4,764,907 , GRCh37.p13 chr12: 4,864,047-4,874,073 GALNT8
    nsv5857093copy number variation1nstd209human GRCh38 chr12: 4,752,181-4,756,380 , GRCh37.p13 chr12: 4,861,347-4,865,546 GALNT8
    nsv5854963copy number variation1nstd209human GRCh38 chr12: 4,755,081-4,757,680 , GRCh37.p13 chr12: 4,864,247-4,866,846 GALNT8
    nsv5710752mobile element insertion2nstd211human GRCh38 chr12: 4,734,688-4,734,688 , GRCh37.p13 chr12: 4,843,854-4,843,854 GALNT8
    nsv5662657insertion1nstd207human GRCh38 chr12: 4,732,977-4,732,977 , GRCh37.p13 chr12: 4,842,143-4,842,143 GALNT8
    nsv5661978insertion1nstd207human GRCh38 chr12: 4,734,671-4,734,671 , GRCh37.p13 chr12: 4,843,837-4,843,837 GALNT8
    nsv5646709insertion1nstd207human GRCh38 chr12: 4,732,593-4,732,593 , GRCh37.p13 chr12: 4,841,759-4,841,759 GALNT8
    nsv5645655insertion1nstd207human GRCh38 chr12: 4,732,424-4,732,424 , GRCh37.p13 chr12: 4,841,590-4,841,590 GALNT8
    nsv5503070copy number variation1nstd206human GRCh38 chr12: 4,750,251-4,764,110 , GRCh37.p13 chr12: 4,859,417-4,873,276 GALNT8
    nsv5499462copy number variation1nstd206human GRCh38 chr12: 4,743,821-4,756,873 , GRCh37.p13 chr12: 4,852,987-4,866,039 GALNT8
    nsv5420125mobile element insertion1nstd206human GRCh38 chr12: 4,734,688-4,734,739 , GRCh37.p13 chr12: 4,843,854-4,843,905 GALNT8
    nsv5381764copy number variation1nstd102humanPathogenic GRCh37 chr12: 3,619,010-5,221,363 , GRCh38.p12 chr12: 3,509,844-5,112,197 OTUD4P1, LOC105369612, 30 more genes
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