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Items: 1 to 20 of 163

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5912852copy number variation1nstd209human GRCh38 chr8: 96,145,964-96,147,140 , GRCh37.p13 chr8: 97,158,192-97,159,368 GDF6
    nsv5372026translocation1nstd200human GRCh38 chr8: 96,148,533-96,148,533 , GRCh38 chr8: 96,150,479-96,150,479 , GRCh37.p13 chr8: 97,160,761-97,160,761 , GRCh37.p13 chr8: 97,162,707-97,162,707 GDF6
    nsv5372025translocation1nstd200human GRCh38 chr8: 96,148,276-96,148,276 , GRCh38 chr8: 96,150,449-96,150,449 , GRCh37.p13 chr8: 97,160,504-97,160,504 , GRCh37.p13 chr8: 97,162,677-97,162,677 GDF6
    nsv5036483inversion1nstd200human GRCh38 chr8: 71,454,844-121,935,245 , GRCh37.p13 chr8: 72,367,079-122,947,484 , LINC01617, 636 more genes
    nsv5035989inversion1nstd200human GRCh38 chr8: 74,949,087-131,777,713 , GRCh37.p13 chr8: 75,861,322-132,789,960 , MIR7705, 715 more genes
    nsv4961366copy number variation1nstd200human GRCh38 chr8: 96,145,966-96,147,141 , GRCh37.p13 chr8: 97,158,194-97,159,369 GDF6
    nsv4822531copy number variation1nstd200human GRCh37 chr8: 97,158,194-97,159,369 , GRCh38.p12 chr8: 96,145,966-96,147,141 GDF6
    nsv4729502copy number variation1nstd102humanLikely pathogenic GRCh37 chr8: 95,803,280-97,802,022 , GRCh38.p12 chr8: 94,791,052-96,789,794 SDC2, UQCRB, 29 more genes
    nsv4674970copy number variation1nstd102humanLikely pathogenic GRCh37 chr8: 96,646,399-98,973,327 , GRCh38.p12 chr8: 95,634,171-97,961,099 MATN2, SDC2, 26 more genes
    nsv4578266copy number variation1nstd102humanPathogenic GRCh37 chr8: 97,154,645-98,155,535 , GRCh38.p12 chr8: 96,142,417-97,143,307 LOC105375652, LOC102724804, 10 more genes
    nsv4456811copy number variation1nstd102humanPathogenic GRCh37 chr8: 31,936,551-146,295,771 , GRCh38.p12 chr8: 32,079,035-145,070,385 TERF1, LOC107986945, 1511 more genes
    nsv4349554copy number variation2nstd102humanPathogenic GRCh37 chr8: 158,048-146,295,771 , GRCh38.p12 chr8: 208,048-145,070,385 LOC101929488, TEX15, 2105 more genes
    nsv4332062inversion1nstd166human GRCh37.p13 chr8: 70,438,609-99,073,700 , GRCh38.p12 chr8: 69,526,374-98,061,472 , FTH1P11, 375 more genes
    nsv4318515inversion1nstd166human GRCh37.p13 chr8: 75,861,320-132,789,960 , GRCh38.p12 chr8: 74,949,085-131,777,713 , ANXA13, 716 more genes
    nsv4169242copy number variation1nstd166human GRCh37.p13 chr8: 97,158,194-97,159,369 , GRCh38.p12 chr8: 96,145,966-96,147,141 GDF6
    nsv3923310copy number variation1nstd102humanPathogenic NCBI36 chr8: 166,452-146,264,902 , GRCh38 chr8: 226,452-145,068,712 , GRCh37 chr8: 176,452-146,294,098 LOC112268023, RPL23AP96, 2105 more genes
    nsv3922992copy number variation1nstd102humanPathogenic NCBI36 chr8: 97,147,297-98,358,385 , GRCh38 chr8: 96,065,893-97,276,981 , GRCh37 chr8: 97,078,121-98,289,209 UQCRB-AS1, TUBBP7, 14 more genes
    nsv3921868copy number variation1nstd102humanPathogenic NCBI36 chr8: 93,836,936-98,873,536 , GRCh38 chr8: 92,755,532-97,792,132 , GRCh37 chr8: 93,767,760-98,804,360 MIR8084, GEM, 75 more genes
    nsv3919841copy number variation1nstd102humanPathogenic GRCh38 chr8: 78,614,077-145,054,634 , GRCh37 chr8: 79,526,312-146,280,020 , NCBI36 chr8: 79,688,867-146,250,824 LY6S-AS1, LOC107984017, 911 more genes
    nsv3919282copy number variation1nstd102humanPathogenic GRCh37 chr8: 191,530-146,280,020 , GRCh38 chr8: 241,530-145,054,634 , NCBI36 chr8: 181,530-146,250,824 MIR4662B, LOC101927845, 2104 more genes
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