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Items: 1 to 20 of 139

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112766copy number variation1nstd102humannot provided GRCh37 chr11: 77,617,820-77,784,237 , GRCh38.p12 chr11: 77,906,774-78,073,191 KCTD14, NDUFC2-KCTD14, 3 more genes
    nsv5970149insertion1nstd209human GRCh38 chr11: 78,078,728-78,078,728 , GRCh37.p13 chr11: 77,789,774-77,789,774 NDUFC2, NDUFC2-KCTD14
    nsv5907740copy number variation1nstd209human GRCh38 chr11: 78,068,581-78,068,920 , GRCh37.p13 chr11: 77,779,627-77,779,966 NDUFC2, THRSP, 1 more genes
    nsv5701623mobile element insertion1nstd211human GRCh38 chr11: 78,069,931-78,069,931 , GRCh37.p13 chr11: 77,780,977-77,780,977 NDUFC2, NDUFC2-KCTD14
    nsv5503414copy number variation1nstd206human GRCh38 chr11: 78,073,660-78,074,426 , GRCh37.p13 chr11: 77,784,706-77,785,472 NDUFC2, NDUFC2-KCTD14
    nsv5410202mobile element insertion1nstd206human GRCh38 chr11: 78,069,931-78,069,934 , GRCh37.p13 chr11: 77,780,977-77,780,980 NDUFC2, NDUFC2-KCTD14
    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
    nsv4989069copy number variation1nstd200human GRCh38 chr11: 77,925,632-78,075,017 , GRCh37.p13 chr11: 77,636,678-77,786,063 INTS4, NDUFC2, 3 more genes
    nsv4989067copy number variation1nstd200human GRCh38 chr11: 77,839,766-78,289,807 , GRCh37.p13 chr11: 77,550,812-78,000,853 KCTD21-AS1, NDUFC2, 13 more genes
    nsv4844562copy number variation1nstd200human GRCh37 chr11: 77,779,629-77,779,967 , GRCh38.p12 chr11: 78,068,583-78,068,921 NDUFC2, THRSP, 1 more genes
    nsv4842769copy number variation1nstd200human GRCh37 chr11: 77,550,812-78,000,853 , GRCh38.p12 chr11: 77,839,766-78,289,807 KCTD14, THRSP, 13 more genes
    nsv4729234copy number variation1nstd102humanUncertain significance GRCh37 chr11: 77,575,261-77,902,589 , GRCh38.p12 chr11: 77,864,215-78,191,543 LOC105369401, KCTD21, 12 more genes
    nsv4490842mobile element insertion1nstd166human GRCh37.p13 chr11: 77,780,966-77,780,966 , GRCh38.p12 chr11: 78,069,920-78,069,920 NDUFC2, NDUFC2-KCTD14
    nsv4455314copy number variation2nstd102humanUncertain significance GRCh37 chr11: 77,410,575-77,785,783 , GRCh38.p12 chr11: 77,699,530-78,074,737 FTH1P16, AAMDC, 8 more genes
    nsv4381100copy number variation1nstd173human GRCh37 chr11: 77,643,952-77,834,894 , GRCh38.p12 chr11: 77,932,906-78,123,848 KCTD14, NDUFC2-KCTD14, 5 more genes
    nsv4377670copy number variation1nstd173human GRCh37 chr11: 77,639,679-77,834,894 , GRCh38.p12 chr11: 77,928,633-78,123,848 NDUFC2, ALG8, 5 more genes
    nsv4196428copy number variation1nstd166human GRCh37.p13 chr11: 77,636,680-77,786,061 , GRCh38.p12 chr11: 77,925,634-78,075,015 NDUFC2, THRSP, 3 more genes
    nsv3921121copy number variation1nstd102humanPathogenic GRCh38 chr11: 75,941,754-98,357,960 , NCBI36 chr11: 75,330,446-97,733,898 , GRCh37 chr11: 75,652,798-98,228,688 LOC105369441, RNU6-1135P, 296 more genes
    nsv3915804copy number variation1nstd102humanPathogenic GRCh37 chr11: 71,680,927-77,943,941 , NCBI36 chr11: 71,358,575-77,621,589 , GRCh38 chr11: 71,969,881-78,232,895 TPBGL, MAP6, 173 more genes
    nsv3908873copy number variation2nstd102humanPathogenic GRCh37 chr11: 230,616-134,938,470 , GRCh38.p12 chr11: 230,616-135,068,576 IGHMBP2, SYTL2, 2829 more genes
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