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Items: 1 to 20 of 201

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5911562copy number variation1nstd209human GRCh38 chr8: 89,783,705-89,783,787 , GRCh37.p13 chr8: 90,795,933-90,796,015 RIPK2
    nsv5695399mobile element insertion2nstd211human GRCh38 chr8: 89,790,050-89,790,050 , GRCh37.p13 chr8: 90,802,278-90,802,278 RIPK2
    nsv5397405mobile element insertion1nstd206human GRCh38 chr8: 89,790,050-89,790,101 , GRCh37.p13 chr8: 90,802,278-90,802,329 RIPK2
    nsv5344552translocation1nstd200human GRCh37 chr8: 90,796,018-90,796,018 , GRCh37 chr8: 90,795,933-90,795,933 , GRCh38.p12 chr8: 89,783,790-89,783,790 , GRCh38.p12 chr8: 89,783,705-89,783,705 RIPK2
    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
    nsv4729552copy number variation1nstd102humanUncertain significance GRCh37 chr8: 88,194,550-91,779,543 , GRCh38.p12 chr8: 87,182,322-90,767,315 RIPK2, RNU6-925P, 29 more genes
    nsv4675461copy number variation1nstd102humanUncertain significance GRCh37 chr8: 90,758,337-91,556,317 , GRCh38.p12 chr8: 89,746,109-90,544,089 OSGIN2, RNU6-925P, 9 more genes
    nsv4493492mobile element insertion1nstd166human GRCh37.p13 chr8: 90,772,783-90,772,783 , GRCh38.p12 chr8: 89,760,555-89,760,555 RIPK2
    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
    nsv4406576copy number variation1nstd174human GRCh37 chr8: 90,471,789-90,783,871 , GRCh38.p12 chr8: 89,459,560-89,771,643 RIPK2, LOC112268015, 2 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
    nsv4164346copy number variation1nstd166human GRCh37.p13 chr8: 90,779,899-90,780,059 , GRCh38.p12 chr8: 89,767,671-89,767,831 RIPK2
    nsv4163144copy number variation1nstd166human GRCh37.p13 chr8: 90,786,209-90,786,298 , GRCh38.p12 chr8: 89,773,981-89,774,070 RIPK2
    nsv3969214copy number variation1nstd168human GRCh38 chr8: 89,724,778-89,758,258 , GRCh37.p13 chr8: 90,737,006-90,770,486 RIPK2, PARAIL
    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
    nsv3923011copy number variation1nstd102humanPathogenic GRCh38 chr8: 66,171,669-93,505,509 , GRCh37 chr8: 67,083,904-94,517,737 , NCBI36 chr8: 67,246,458-94,586,913 CA3, HAUS1P3, 353 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
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