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Items: 1 to 20 of 143

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    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
    nsv3909544copy number variation1nstd102humanUncertain significance GRCh37 chr19: 29,341,513-29,818,674 , GRCh38.p12 chr19: 28,850,606-29,327,767 LINC00906, UQCRFS1, 6 more genes
    nsv3908619copy number variation1nstd102humanLikely pathogenic GRCh37 chr19: 28,271,107-31,110,233 , GRCh38.p12 chr19: 27,780,199-30,619,326 CCNE1, UQCRFS1, 31 more genes
    nsv3904885copy number variation1nstd102humanPathogenic GRCh37 chr19: 68,029-59,110,290 , GRCh38.p12 chr19: 68,029-58,598,923 ZNF321P, ZNF861P, 2443 more genes
    nsv3903203copy number variation1nstd102humanPathogenic GRCh37 chr19: 260,912-59,097,160 , GRCh38.p12 chr19: 260,912-58,585,793 BABAM1, BEST2, 2426 more genes
    nsv3903092copy number variation2nstd102humanPathogenic GRCh37 chr19: 260,912-58,956,888 , GRCh38.p12 chr19: 260,912-58,445,521 LENG8, SYDE1, 2408 more genes
    nsv3893300copy number variation1nstd102humanUncertain significance GRCh37 chr19: 29,083,484-31,804,809 , GRCh38.p12 chr19: 28,592,577-31,313,903 LOC105372358, TAF9P3, 29 more genes
    nsv3163717copy number variation1nstd151human GRCh37 chr19: 29,698,452-29,699,070 , GRCh38.p12 chr19: 29,207,545-29,208,163 UQCRFS1
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