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Items: 1 to 20 of 141

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7069002inversion1nstd229human GRCh38 chr19: 29,595,991-29,615,140 , GRCh37.p13 chr19: 30,086,898-30,106,047 POP4
    nsv7017867copy number variation1nstd229human GRCh38 chr19: 29,590,937-29,606,232 , GRCh37.p13 chr19: 30,081,844-30,097,139 POP4
    nsv7015607copy number variation1nstd229human GRCh38 chr19: 29,595,901-29,608,500 , GRCh37.p13 chr19: 30,086,808-30,099,407 POP4
    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
    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
    nsv5198990mobile element insertion1nstd203human GRCh38 chr19: 29,608,589-29,608,606 , GRCh37.p13 chr19: 30,099,496-30,099,513 POP4
    nsv5024522copy number variation1nstd200human GRCh38 chr19: 29,599,281-29,615,329 , GRCh37.p13 chr19: 30,090,188-30,106,236 POP4
    nsv5024519copy number variation1nstd200human GRCh38 chr19: 28,925,173-32,768,971 , GRCh37.p13 chr19: 29,416,080-33,259,877 , LOC105372355, 53 more genes
    nsv5020229copy number variation1nstd200human GRCh38 chr19: 29,608,212-29,613,454 , GRCh37.p13 chr19: 30,099,119-30,104,361 POP4
    nsv5020164copy number variation1nstd200human GRCh38 chr19: 28,377,231-29,769,380 , GRCh37.p13 chr19: 28,868,138-30,260,287 , LINC00906, 18 more genes
    nsv4861161copy number variation1nstd200human GRCh37 chr19: 30,099,119-30,104,361 , GRCh38.p12 chr19: 29,608,212-29,613,454 POP4
    nsv4729940copy number variation1nstd102humanUncertain significance GRCh37 chr19: 29,739,728-31,053,524 , GRCh38.p12 chr19: 29,248,821-30,562,617 PLEKHF1, RPL9P32, 12 more genes
    nsv4702925copy number variation1nstd195human GRCh38.p12 chr19: 29,514,544-29,719,294 , GRCh37 chr19: 30,005,451-30,210,201 POP4, PLEKHF1, 4 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
    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
    nsv3913730copy number variation1nstd102humanPathogenic NCBI36 chr19: 11,199,618-49,821,491 , GRCh37 chr19: 11,338,618-45,129,651 , GRCh38 chr19: 11,227,942-44,626,354 BCKDHA, ADGRE5, 1102 more genes
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