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Items: 1 to 20 of 178

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5709679mobile element insertion1nstd211human GRCh38 chr8: 94,258,368-94,258,368 , GRCh37.p13 chr8: 95,270,596-95,270,596 GEM
    nsv5405434mobile element insertion1nstd206human GRCh38 chr8: 94,258,368-94,258,419 , GRCh37.p13 chr8: 95,270,596-95,270,647 GEM
    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
    nsv4675900copy number variation1nstd102humanUncertain significance GRCh37 chr8: 94,810,526-95,397,957 , GRCh38.p12 chr8: 93,798,298-94,385,729 RPL34P18, MIR378D2, 12 more genes
    nsv4607529copy number variation1nstd183human GRCh37 chr8: 95,184,567-95,304,598 , GRCh38.p12 chr8: 94,172,339-94,292,370 CDH17, RPL6P23, 2 more genes
    nsv4605897copy number variation1nstd183human GRCh37 chr8: 95,261,486-95,261,830 , GRCh38.p12 chr8: 94,249,258-94,249,602 GEM
    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
    nsv4379230copy number variation1nstd173human GRCh37 chr8: 94,729,725-96,353,188 , GRCh38.p12 chr8: 93,717,497-95,340,960 , TMEM67, 39 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
    nsv4169489copy number variation1nstd166human GRCh37.p13 chr8: 95,274,355-95,279,636 , GRCh38.p12 chr8: 94,262,127-94,267,408 GEM
    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
    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
    nsv3920272copy number variation1nstd102humanPathogenic NCBI36 chr8: 94,119,579-96,749,186 , GRCh37 chr8: 94,050,403-96,680,010 , GRCh38 chr8: 93,038,175-95,667,782 PLEKHF2, INTS8, 48 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
    nsv3919200copy number variation1nstd102humanPathogenic GRCh38 chr8: 241,530-145,049,449 , GRCh37 chr8: 191,530-146,274,835 , NCBI36 chr8: 181,530-146,245,639 LOC112268023, LOC105375925, 2103 more genes
    nsv3916978copy number variation1nstd102humanPathogenic GRCh38 chr8: 86,300,584-137,022,587 , NCBI36 chr8: 87,381,929-138,104,012 , GRCh37 chr8: 87,312,813-138,034,830 MIR5194, TRS-AGA2-5, 601 more genes
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