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Items: 1 to 20 of 151

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7012800copy number variation1nstd229human GRCh38 chr19: 28,848,801-29,336,200 , GRCh37.p13 chr19: 29,339,708-29,827,107 LINC01532, UQCRFS1, 6 more genes
    nsv7007067copy number variation1nstd229human GRCh38 chr19: 28,961,373-29,290,066 , GRCh37.p13 chr19: 29,452,280-29,780,973 VSTM2B-DT, UQCRFS1-DT, 6 more genes
    nsv7005429copy number variation1nstd229human GRCh38 chr19: 28,956,435-29,334,441 , GRCh37.p13 chr19: 29,447,342-29,825,348 UQCRFS1, RN7SL340P, 6 more genes
    nsv7004950copy number variation1nstd229human GRCh38 chr19: 29,205,078-29,205,105 , GRCh37.p13 chr19: 29,695,985-29,696,012 UQCRFS1
    nsv6527526copy number variation1nstd223human GRCh38 chr19: 28,925,173-32,768,942 , GRCh37.p13 chr19: 29,416,080-33,259,848 DPY19L3, CCNE1, 50 more genes
    nsv6526233copy number variation1nstd223human GRCh38 chr19: 28,377,231-29,769,380 , GRCh37.p13 chr19: 28,868,138-30,260,287 LINC01532, C19orf12, 16 more genes
    nsv6519567copy number variation1nstd223human GRCh38 chr19: 29,205,077-29,205,103 , GRCh37.p13 chr19: 29,695,984-29,696,010 UQCRFS1
    nsv6290300copy number variation1nstd102humanPathogenic GRCh37 chr19: 19,546,923-41,313,229 , GRCh38.p12 chr19: 19,436,114-40,807,324 ZNF420, LOC105372330, 574 more genes
    nsv5024519copy number variation1nstd200human GRCh38 chr19: 28,925,173-32,768,971 , GRCh37.p13 chr19: 29,416,080-33,259,877 , LOC105372355, 53 more genes
    nsv5020207copy number variation1nstd200human GRCh38 chr19: 29,127,176-29,204,206 , GRCh37.p13 chr19: 29,618,083-29,695,113 UQCRFS1
    nsv5020164copy number variation1nstd200human GRCh38 chr19: 28,377,231-29,769,380 , GRCh37.p13 chr19: 28,868,138-30,260,287 , LINC00906, 18 more genes
    nsv4712666copy number variation1nstd195human GRCh37 chr19: 29,629,551-29,716,751 , GRCh38.p12 chr19: 29,138,644-29,225,844 UQCRFS1, UQCRFS1-DT
    nsv4708147copy number variation1nstd195human GRCh37 chr19: 29,629,301-29,717,351 , GRCh38.p12 chr19: 29,138,394-29,226,444 UQCRFS1, UQCRFS1-DT
    nsv4676277copy number variation1nstd102humanUncertain significance GRCh37 chr19: 29,118,589-29,791,099 , GRCh38.p12 chr19: 28,627,682-29,300,192 LINC01532, RNA5SP470, 8 more genes
    nsv4630420copy number variation1nstd183human GRCh37 chr19: 27,749,407-30,499,419 , GRCh38.p12 chr19: 27,258,499-30,008,512 , C19orf12, 32 more genes
    nsv4457372copy number variation1nstd102humanPathogenic GRCh37 chr19: 28,271,106-49,213,832 , GRCh38.p12 chr19: 27,780,198-48,710,575 ZNF461, LOC101927572, 735 more genes
    nsv4341828sequence alteration1nstd166human GRCh37.p13 chr19: 29,645,636-29,893,989 , GRCh38.p12 chr19: 29,154,729-29,403,082 UQCRFS1, VSTM2B-DT, 2 more genes
    nsv3920776copy number variation1nstd102humanLikely pathogenic NCBI36 chr19: 34,234,635-37,150,342 , GRCh37 chr19: 29,542,795-32,458,502 , GRCh38 chr19: 29,051,888-31,967,596 CCNE1, UQCRFS1, 30 more genes
    nsv3919618copy number variation1nstd102humanUncertain significance NCBI36 chr19: 32,962,986-39,966,686 , GRCh38 chr19: 27,780,238-34,783,942 , GRCh37 chr19: 28,271,146-35,274,846 LINC00906, TDRD12, 112 more genes
    nsv3914228copy number variation1nstd102humanPathogenic NCBI36 chr19: 17,148,576-40,106,894 , GRCh38 chr19: 17,176,767-34,924,150 , GRCh37 chr19: 17,287,576-35,415,054 LOC105372355, SUGP2, 411 more genes
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