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Items: 1 to 20 of 322

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6115334mobile element insertion1nstd186human GRCh37 chr19: 36,971,524-36,971,524 , GRCh38.p12 chr19: 36,480,622-36,480,622 ZNF566
    nsv5979106insertion1nstd209human GRCh38 chr19: 36,480,622-36,480,622 , GRCh37.p13 chr19: 36,971,524-36,971,524 ZNF566
    nsv5967559insertion1nstd209human GRCh38 chr19: 36,477,536-36,477,536 , GRCh37.p13 chr19: 36,968,438-36,968,438 ZNF566
    nsv5938569copy number variation1nstd209human GRCh38 chr19: 36,489,086-36,529,068 , GRCh37.p13 chr19: 36,979,988-37,019,970 ZNF566, ZNF260, 2 more genes
    nsv5881974copy number variation1nstd209human GRCh38 chr19: 36,447,926-36,449,225 , GRCh37.p13 chr19: 36,938,828-36,940,127 ZNF566
    nsv5877833copy number variation1nstd209human GRCh38 chr19: 36,448,426-36,450,025 , GRCh37.p13 chr19: 36,939,328-36,940,927 ZNF566
    nsv5874399copy number variation2nstd209human GRCh38 chr19: 36,457,581-36,458,680 , GRCh37.p13 chr19: 36,948,483-36,949,582 ZNF566
    nsv5873736copy number variation1nstd209human GRCh38 chr19: 36,442,217-36,443,416 , GRCh37.p13 chr19: 36,933,119-36,934,318 ZNF566
    nsv5869770copy number variation1nstd209human GRCh38 chr19: 36,488,801-36,515,655 , GRCh37.p13 chr19: 36,979,703-37,006,557 ZNF566, ZNF260, 2 more genes
    nsv5868907copy number variation1nstd209human GRCh38 chr19: 36,452,201-36,453,250 , GRCh37.p13 chr19: 36,943,103-36,944,152 ZNF566
    nsv5707745mobile element insertion1nstd211human GRCh38 chr19: 36,480,635-36,480,635 , GRCh37.p13 chr19: 36,971,537-36,971,537 ZNF566
    nsv5704764mobile element insertion2nstd211human GRCh38 chr19: 36,450,040-36,450,040 , GRCh37.p13 chr19: 36,940,942-36,940,942 ZNF566
    nsv5664109insertion1nstd207human GRCh38 chr19: 36,480,622-36,480,622 , GRCh37.p13 chr19: 36,971,524-36,971,524 ZNF566
    nsv5650151insertion1nstd207human GRCh38 chr19: 36,457,966-36,457,966 , GRCh37.p13 chr19: 36,948,868-36,948,868 ZNF566
    nsv5602987copy number variation1nstd207human GRCh38 chr19: 36,466,904-36,469,374 , GRCh37.p13 chr19: 36,957,806-36,960,276 ZNF566
    nsv5532788copy number variation1nstd206human GRCh38 chr19: 36,443,452-36,443,591 , GRCh37.p13 chr19: 36,934,354-36,934,493 ZNF566
    nsv5528789copy number variation1nstd206human GRCh38 chr19: 36,489,215-36,529,071 , GRCh37.p13 chr19: 36,980,117-37,019,973 CTBP2P7, ZNF566, 2 more genes
    nsv5524458copy number variation1nstd206human GRCh38 chr19: 36,466,921-36,469,365 , GRCh37.p13 chr19: 36,957,823-36,960,267 ZNF566
    nsv5523242copy number variation1nstd206human GRCh38 chr19: 36,474,874-36,560,874 , GRCh37.p13 chr19: 36,965,776-37,051,776 ZNF566-AS1, ZNF566, 3 more genes
    nsv5521465copy number variation1nstd206human GRCh38 chr19: 36,453,103-36,453,540 , GRCh37.p13 chr19: 36,944,005-36,944,442 ZNF566
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