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Items: 1 to 20 of 174

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5974799inversion1nstd209human GRCh38 chr19: 12,342,936-19,691,231 , GRCh37.p13 chr19: 12,453,750-19,802,040 , GET3, 322 more genes
    nsv5940186copy number variation1nstd209human GRCh38 chr19: 17,287,380-17,289,048 , GRCh37.p13 chr19: 17,398,189-17,399,857 ANKLE1
    nsv5883085copy number variation1nstd209human GRCh38 chr19: 17,287,542-17,289,041 , GRCh37.p13 chr19: 17,398,351-17,399,850 ANKLE1
    nsv5524045copy number variation1nstd206human GRCh38 chr19: 17,287,380-17,289,053 , GRCh37.p13 chr19: 17,398,189-17,399,862 ANKLE1
    nsv5391794copy number variation1nstd186human GRCh37 chr19: 17,398,221-17,399,777 , GRCh38.p12 chr19: 17,287,412-17,288,968 ANKLE1
    nsv5323460copy number variation1nstd204human GRCh38.p13 chr19: 17,287,373-17,288,997 , GRCh37.p13 chr19: 17,398,182-17,399,806 ANKLE1
    nsv5299651copy number variation1nstd204human GRCh38.p13 chr19: 16,996,101-18,292,600 , GRCh37.p13 chr19: 17,106,911-18,403,410 ANO8, MPV17L2, 57 more genes
    nsv5293042copy number variation1nstd204human GRCh38.p13 chr19: 17,178,501-17,350,400 , GRCh37.p13 chr19: 17,289,310-17,461,209 NR2F6, ABHD8, 11 more genes
    nsv5286520copy number variation1nstd204human GRCh38.p13 chr19: 17,091,201-17,638,100 , GRCh37.p13 chr19: 17,202,011-17,748,909 PGLS, LOC105372298, 27 more genes
    nsv5041043inversion1nstd200human GRCh38 chr19: 11,963,569-20,150,886 , GRCh37.p13 chr19: 12,074,384-20,193,556 , USE1, 369 more genes
    nsv5012137copy number variation1nstd200human GRCh38 chr19: 17,287,410-17,288,968 , GRCh37.p13 chr19: 17,398,219-17,399,777 ANKLE1
    nsv4860563copy number variation1nstd200human GRCh37 chr19: 17,398,217-17,399,779 , GRCh38.p12 chr19: 17,287,408-17,288,970 ANKLE1
    nsv4729750copy number variation1nstd102humanPathogenic GRCh37 chr19: 14,286,624-20,956,753 , GRCh38.p12 chr19: 14,175,812-20,773,947 LOC105372309, RAB8A, 269 more genes
    nsv4667623copy number variation1nstd186human GRCh37 chr19: 17,398,189-17,399,858 , GRCh38.p12 chr19: 17,287,380-17,289,049 ANKLE1
    nsv4620773copy number variation1nstd183human GRCh37 chr19: 17,398,189-17,399,858 , GRCh38.p12 chr19: 17,287,380-17,289,049 ANKLE1
    nsv4537413copy number variation1nstd166human GRCh37.p13 chr19: 17,398,193-17,399,887 , GRCh38.p12 chr19: 17,287,384-17,289,078 ANKLE1
    nsv4457871copy number variation1nstd102humanUncertain significance GRCh37 chr19: 16,875,725-17,477,318 , GRCh38.p12 chr19: 16,764,914-17,366,509 HAUS8, MYO9B, 19 more genes
    nsv4427216copy number variation1nstd174human GRCh37 chr19: 17,398,053-17,400,842 , GRCh38.p12 chr19: 17,287,244-17,290,033 ANKLE1
    nsv4267964copy number variation1nstd166human GRCh37.p13 chr19: 17,395,284-17,395,563 , GRCh38.p12 chr19: 17,284,475-17,284,754 ANKLE1
    nsv4267793copy number variation1nstd166human GRCh37.p13 chr19: 17,373,062-17,411,604 , GRCh38.p12 chr19: 17,262,253-17,300,795 ANKLE1, USHBP1, 2 more genes
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