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Items: 1 to 20 of 710

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7144991insertion1nstd232human GRCh37.p13 chr11: 642,745-642,745 , GRCh38.p12 chr11: 642,745-642,745 , GRCh38.p12 chr11|NT_187586.1: 172,614-172,614 DEAF1
    nsv7137204copy number variation1nstd102humanPathogenic GRCh37 chr11: 268,586-748,873 , GRCh38.p12 chr11: 268,586-748,873 PKP3, RN7SL838P, 32 more genes
    nsv7094098copy number variation1nstd102humanPathogenic GRCh37 chr11: 674,516-674,803 , GRCh38.p12 chr11: 674,516-674,803 , GRCh38.p12 chr11|NT_187586.1: 206,441-206,728 DEAF1
    nsv7094013copy number variation1nstd102humanPathogenic GRCh37 chr11: 694,739-695,047 , GRCh38.p12 chr11: 694,739-695,047 DEAF1, TMEM80
    nsv7093939copy number variation1nstd102humanPathogenic GRCh37 chr11: 678,674-681,109 , GRCh38.p12 chr11: 678,674-681,109 DEAF1
    nsv7093934copy number variation1nstd102humanUncertain significance GRCh37 chr11: 653,942-654,071 , GRCh38.p12 chr11: 653,942-654,071 , GRCh38.p12 chr11|NT_187586.1: 185,698-185,827 DEAF1
    nsv7093930copy number variation1nstd102humanUncertain significance GRCh37 chr11: 644,550-795,006 , GRCh38.p12 chr11: 644,550-795,006 LOC105376509, GATD1, 7 more genes
    nsv7093693copy number variation1nstd102humanUncertain significance GRCh37 chr11: 532,636-819,925 , GRCh38.p12 chr11: 532,636-819,925 , GRCh38.p12 chr11|NT_187586.1: 62,277-209,248 HRAS, LRRC56, 25 more genes
    nsv7068164inversion1nstd229human GRCh38 chr11: 525,138-982,890 , GRCh37.p13 chr11: 525,138-982,890 DRD4, LMNTD2-AS1, 32 more genes
    nsv7067944inversion1nstd229human GRCh38 chr11: 288,558-695,861 , GRCh37.p13 chr11: 288,558-695,861 IRF7, TMEM80, 28 more genes
    nsv7058883inversion1nstd229human GRCh38 chr11: 499,565-690,606 , GRCh37.p13 chr11: 499,565-690,606 LOC143666, DEAF1, 13 more genes
    nsv6898065copy number variation1nstd229human GRCh38 chr11: 650,981-655,196 , GRCh37.p13 chr11: 650,981-655,196 DEAF1
    nsv6896730copy number variation1nstd229human GRCh38 chr11: 659,997-673,538 , GRCh37.p13 chr11: 659,997-673,538 DEAF1
    nsv6895084copy number variation1nstd229human GRCh38 chr11: 697,537-703,716 , GRCh37.p13 chr11: 697,537-703,716 TMEM80, DEAF1
    nsv6894829copy number variation1nstd229human GRCh38 chr11: 654,227-655,160 , GRCh37.p13 chr11: 654,227-655,160 DEAF1
    nsv6894061copy number variation1nstd229human GRCh38 chr11: 677,327-677,794 , GRCh37.p13 chr11: 677,327-677,794 DEAF1
    nsv6893657copy number variation1nstd229human GRCh38 chr11: 627,701-648,400 , GRCh37.p13 chr11: 627,701-648,400 DEAF1, SCT, 1 more genes
    nsv6892559copy number variation1nstd229human GRCh38 chr11: 670,169-670,221 , GRCh37.p13 chr11: 670,169-670,221 DEAF1
    nsv6890788copy number variation1nstd229human GRCh38 chr11: 661,570-669,993 , GRCh37.p13 chr11: 661,570-669,993 DEAF1
    nsv6889798copy number variation1nstd229human GRCh38 chr11: 694,701-722,900 , GRCh37.p13 chr11: 694,701-722,900 TMEM80, EPS8L2, 1 more genes
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