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Items: 1 to 20 of 120

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5970408inversion1nstd209human GRCh38 chr19: 2,282,477-7,636,587 , GRCh37.p13 chr19: 2,282,476-7,701,473 , TLE5, 195 more genes
    nsv5968665insertion1nstd209human GRCh38 chr19: 7,495,078-7,495,078 , GRCh37.p13 chr19: 7,559,964-7,559,964 PEX11G
    nsv5938881copy number variation1nstd209human GRCh38 chr19: 7,493,228-7,493,539 , GRCh37.p13 chr19: 7,558,114-7,558,425 PEX11G
    nsv5932336copy number variation1nstd209human GRCh38 chr19: 7,473,682-7,475,104 , GRCh37.p13 chr19: 7,538,568-7,539,990 PEX11G, ARHGEF18
    nsv5596264copy number variation1nstd207human GRCh38 chr19: 7,495,006-7,495,077 , GRCh37.p13 chr19: 7,559,892-7,559,963 PEX11G
    nsv5288851copy number variation1nstd204human GRCh38.p13 chr19: 7,060,701-7,599,200 , GRCh37.p13 chr19: 7,060,712-7,664,086 , INSR, 9 more genes
    nsv5179185mobile element insertion1nstd203human GRCh38 chr19: 7,490,998-7,491,039 , GRCh37.p13 chr19: 7,555,884-7,555,925 PEX11G
    nsv5166924mobile element insertion1nstd203human GRCh38 chr19: 7,493,200-7,493,211 , GRCh37.p13 chr19: 7,558,086-7,558,097 PEX11G
    nsv5027562copy number variation1nstd200human GRCh38 chr19: 7,495,153-7,495,281 , GRCh37.p13 chr19: 7,560,039-7,560,167 PEX11G
    nsv5027561copy number variation1nstd200human GRCh38 chr19: 7,485,460-7,486,686 , GRCh37.p13 chr19: 7,550,346-7,551,572 PEX11G
    nsv4629101copy number variation1nstd183human GRCh37 chr19: 7,397,015-7,925,985 , GRCh38.p12 chr19: 7,332,094-7,861,099 , PEX11G, 27 more genes
    nsv4621573copy number variation1nstd183human GRCh37 chr19: 7,557,665-7,558,070 , GRCh38.p12 chr19: 7,492,779-7,493,184 PEX11G
    nsv4388129copy number variation1nstd173human GRCh37 chr19: 7,480,077-7,681,143 , GRCh38.p12 chr19: 7,415,191-7,616,257 PNPLA6, ARHGEF18, 7 more genes
    nsv4261533copy number variation1nstd166human GRCh37.p13 chr19: 7,541,582-7,545,906 , GRCh38.p12 chr19: 7,476,696-7,481,020 ARHGEF18, PEX11G
    nsv3958288insertion1nstd168human GRCh38 chr19: 7,320,154-7,483,541 , GRCh37.p13 chr19: 7,396,129-7,548,427 , ARHGEF18, 1 more genes
    nsv3917314copy number variation1nstd102humanUncertain significance NCBI36 chr19: 7,145,928-7,798,318 , GRCh38 chr19: 7,194,917-7,827,432 , GRCh37 chr19: 7,194,928-7,892,318 CLEC4G, STXBP2, 26 more genes
    nsv3914351copy number variation1nstd102humanPathogenic NCBI36 chr19: 1,923,244-9,620,555 , GRCh38 chr19: 1,972,245-9,648,879 , GRCh37 chr19: 1,972,244-9,759,555 SEMA6B, RANBP3-DT, 299 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
    nsv3903720copy number variation1nstd102humanBenign GRCh37 chr19: 7,528,817-7,589,886 , GRCh38.p12 chr19: 7,463,931-7,525,000 ZNF358, ARHGEF18, 4 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
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