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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5887947copy number variation1nstd209human GRCh38 chr3: 113,951,224-113,951,280 , GRCh37.p13 chr3: 113,670,071-113,670,127 ZDHHC23
    nsv5682759mobile element insertion1nstd211human GRCh38 chr3: 113,981,633-113,981,633 , GRCh37.p13 chr3: 113,700,480-113,700,480 ZDHHC23, CCDC191
    nsv5674224copy number variation1nstd102humanPathogenic GRCh37 chr3: 113,623,035-114,368,128 , GRCh38.p12 chr3: 113,904,188-114,649,281 VPS26AP1, ATOSBP1, 14 more genes
    nsv5436628copy number variation1nstd206human GRCh38 chr3: 113,960,553-113,960,611 , GRCh37.p13 chr3: 113,679,400-113,679,458 ZDHHC23
    nsv5412363mobile element insertion1nstd206human GRCh38 chr3: 113,981,633-113,981,684 , GRCh37.p13 chr3: 113,700,480-113,700,531 CCDC191, ZDHHC23
    nsv5346428translocation1nstd200human GRCh38 chr3: 113,973,478-113,973,478 , GRCh38 chr3: 113,973,535-113,973,535 , GRCh37.p13 chr3: 113,692,325-113,692,325 , GRCh37.p13 chr3: 113,692,382-113,692,382 ZDHHC23, CCDC191
    nsv5081236mobile element insertion1nstd203human GRCh38 chr3: 113,990,455-113,990,471 , GRCh37.p13 chr3: 113,709,302-113,709,318 ZDHHC23, CCDC191
    nsv5036857inversion1nstd200human GRCh38 chr3: 97,392,267-146,717,859 , GRCh37.p13 chr3: 97,111,111-146,435,646 , FBRSL1P1, 801 more genes
    nsv5031637inversion1nstd200human GRCh38 chr3: 112,181,184-125,673,487 , GRCh37.p13 chr3: 111,900,031-125,392,331 , ARHGAP31, 218 more genes
    nsv4914661copy number variation1nstd200human GRCh38 chr3: 113,938,520-114,019,039 , GRCh37.p13 chr3: 113,657,367-113,737,886 LOC105374048, GRAMD1C, 3 more genes
    nsv4794301copy number variation1nstd200human GRCh37 chr3: 113,657,367-113,737,886 , GRCh38.p12 chr3: 113,938,520-114,019,039 GRAMD1C, ZDHHC23, 3 more genes
    nsv4728380copy number variation1nstd102humanPathogenic GRCh37 chr3: 112,135,341-115,509,260 , GRCh38.p12 chr3: 112,416,494-115,790,413 SLC35A5, EIF4E2P2, 51 more genes
    nsv4684086copy number variation1nstd102humanPathogenic GRCh37 chr3: 113,233,952-118,525,556 , GRCh38.p12 chr3: 113,515,105-118,806,709 SIDT1, RNU5E-8P, 55 more genes
    nsv4587017copy number variation2nstd183human GRCh37 chr3: 113,666,273-113,667,425 , GRCh38.p12 chr3: 113,947,426-113,948,578 ZDHHC23, GRAMD1C
    nsv4584665copy number variation1nstd183human GRCh37 chr3: 112,890,620-113,680,951 , GRCh38.p12 chr3: 113,171,773-113,962,104 NEPRO-AS1, SIDT1, 17 more genes
    nsv4578248copy number variation1nstd102humanPathogenic GRCh37 chr3: 112,183,943-115,492,949 , GRCh38.p12 chr3: 112,465,096-115,774,102 ZBTB20, ZBTB20-AS1, 51 more genes
    nsv4468662mobile element insertion1nstd166human GRCh37.p13 chr3: 113,700,469-113,700,469 , GRCh38.p12 chr3: 113,981,622-113,981,622 CCDC191, ZDHHC23
    nsv4450147copy number variation1nstd102humanUncertain significance GRCh37 chr3: 113,594,376-114,060,961 , GRCh38.p12 chr3: 113,875,529-114,342,114 MIR568, CCDC191, 13 more genes
    nsv4395116copy number variation1nstd174human GRCh37 chr3: 113,666,273-113,667,425 , GRCh38.p12 chr3: 113,947,426-113,948,578 GRAMD1C, ZDHHC23
    nsv4317801inversion1nstd166human GRCh37.p13 chr3: 106,160,269-123,476,086 , GRCh38.p12 chr3: 106,441,422-123,757,239 , ADPRH, 270 more genes
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