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Items: 1 to 20 of 232

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5967657insertion1nstd209human GRCh38 chr11: 104,915,863-104,915,863 , GRCh37.p13 chr11: 104,786,590-104,786,590 CASP4LP
    nsv5918104copy number variation1nstd209human GRCh38 chr11: 104,190,618-110,044,159 , GRCh37.p13 chr11: 104,061,346-109,914,884 , CARD18, 71 more genes
    nsv5702028mobile element insertion2nstd211human GRCh38 chr11: 104,915,881-104,915,881 , GRCh37.p13 chr11: 104,786,608-104,786,608 CASP4LP
    nsv5672640copy number variation1nstd102humanPathogenic GRCh37 chr11: 94,153,285-111,965,700 , GRCh38.p12 chr11: 94,420,119-112,094,976 HSPD1P13, CARD17P, 239 more genes
    nsv5646136insertion1nstd207human GRCh38 chr11: 104,915,863-104,915,863 , GRCh37.p13 chr11: 104,786,590-104,786,590 CASP4LP
    nsv5497156copy number variation1nstd206human GRCh38 chr11: 104,887,017-104,911,174 , GRCh37.p13 chr11: 104,757,744-104,781,901 LOC107984380, CASP4LP, 1 more genes
    nsv5400783mobile element insertion1nstd206human GRCh38 chr11: 104,915,863-104,915,863 , GRCh37.p13 chr11: 104,786,590-104,786,590 CASP4LP
    nsv5380796copy number variation1nstd102humanPathogenic GRCh37 chr11: 11,835,569-118,373,112 , GRCh38.p12 chr11: 11,814,022-118,502,397 FAUP4, MMP7, 2031 more genes
    nsv5184481mobile element insertion1nstd203human GRCh38 chr11: 104,901,285-104,901,299 , GRCh37.p13 chr11: 104,772,012-104,772,026 CASP4LP
    nsv5135875mobile element insertion1nstd203human GRCh38 chr11: 104,915,867-104,915,881 , GRCh37.p13 chr11: 104,786,594-104,786,608 CASP4LP
    nsv5134427mobile element insertion1nstd203human GRCh38 chr11: 104,915,865-104,915,881 , GRCh37.p13 chr11: 104,786,592-104,786,608 CASP4LP
    nsv5133372mobile element insertion1nstd203human GRCh38 chr11: 104,915,863-104,915,881 , GRCh37.p13 chr11: 104,786,590-104,786,608 CASP4LP
    nsv5130404mobile element insertion1nstd203human GRCh38 chr11: 104,915,870-104,915,881 , GRCh37.p13 chr11: 104,786,597-104,786,608 CASP4LP
    nsv5127967mobile element insertion1nstd203human GRCh38 chr11: 104,915,866-104,915,881 , GRCh37.p13 chr11: 104,786,593-104,786,608 CASP4LP
    nsv5127742mobile element insertion1nstd203human GRCh38 chr11: 104,915,875-104,915,881 , GRCh37.p13 chr11: 104,786,602-104,786,608 CASP4LP
    nsv5127644mobile element insertion1nstd203human GRCh38 chr11: 104,915,868-104,915,881 , GRCh37.p13 chr11: 104,786,595-104,786,608 CASP4LP
    nsv5127014mobile element insertion1nstd203human GRCh38 chr11: 104,915,864-104,915,881 , GRCh37.p13 chr11: 104,786,591-104,786,608 CASP4LP
    nsv5124572mobile element insertion1nstd203human GRCh38 chr11: 104,915,869-104,915,881 , GRCh37.p13 chr11: 104,786,596-104,786,608 CASP4LP
    nsv5122341mobile element insertion1nstd203human GRCh38 chr11: 104,915,881-104,915,881 , GRCh37.p13 chr11: 104,786,608-104,786,608 CASP4LP
    nsv5122267mobile element insertion1nstd203human GRCh38 chr11: 104,915,862-104,915,881 , GRCh37.p13 chr11: 104,786,589-104,786,608 CASP4LP
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