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Items: 1 to 20 of 207

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5909893copy number variation1nstd209human GRCh38 chr8: 102,239,105-102,239,332 , GRCh37.p13 chr8: 103,251,333-103,251,560 UBR5-DT, RRM2B
    nsv5487611copy number variation1nstd206human GRCh38 chr8: 102,200,979-102,319,280 , GRCh37.p13 chr8: 103,213,207-103,331,508 UBR5, SUMO2P19, 2 more genes
    nsv5372069translocation1nstd200human GRCh38 chr8: 102,239,219-102,239,219 , GRCh38 chr8: 102,239,138-102,239,138 , GRCh37.p13 chr8: 103,251,366-103,251,366 , GRCh37.p13 chr8: 103,251,447-103,251,447 UBR5-DT, RRM2B
    nsv5333703translocation1nstd200human GRCh37 chr8: 103,251,366-103,251,366 , GRCh37 chr8: 103,251,447-103,251,447 , GRCh38.p12 chr8: 102,239,219-102,239,219 , GRCh38.p12 chr8: 102,239,138-102,239,138 UBR5-DT, RRM2B
    nsv5301036copy number variation1nstd204human GRCh38.p13 chr8: 102,226,506-102,371,281 , GRCh37.p13 chr8: 103,238,734-103,383,509 UBR5, SUMO2P19, 2 more genes
    nsv5252661copy number variation1nstd204human GRCh38.p13 chr8: 102,225,776-102,246,926 , GRCh37.p13 chr8: 103,238,004-103,259,154 UBR5-DT, RRM2B, 1 more genes
    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
    nsv4822674copy number variation1nstd200human GRCh37 chr8: 103,259,036-103,259,437 , GRCh38.p12 chr8: 102,246,808-102,247,209 UBR5-DT
    nsv4822673copy number variation1nstd200human GRCh37 chr8: 103,253,188-103,253,648 , GRCh38.p12 chr8: 102,240,960-102,241,420 SUMO2P19, UBR5-DT
    nsv4729735copy number variation1nstd102humanUncertain significance GRCh37 chr8: 103,152,797-103,408,155 , GRCh38.p12 chr8: 102,140,569-102,395,927 LOC112268018, RRM2B, 3 more genes
    nsv4611827copy number variation1nstd183human GRCh37 chr8: 103,264,557-103,265,711 , GRCh38.p12 chr8: 102,252,329-102,253,483 UBR5, UBR5-DT
    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
    nsv4456464copy number variation1nstd102humanUncertain significance GRCh37 chr8: 103,237,328-103,367,599 , GRCh38.p12 chr8: 102,225,100-102,355,371 RRM2B, UBR5, 2 more genes
    nsv4411379copy number variation1nstd174human GRCh37 chr8: 103,109,921-103,331,254 , GRCh38.p12 chr8: 102,097,693-102,319,026 RRM2B, UBR5, 5 more genes
    nsv4408050copy number variation1nstd174human GRCh37 chr8: 103,199,207-103,586,832 , GRCh38.p12 chr8: 102,186,979-102,574,604 ODF1, LOC105375683, 10 more genes
    nsv4385567copy number variation1nstd173human GRCh37 chr8: 103,179,643-103,363,342 , GRCh38.p12 chr8: 102,167,415-102,351,114 UBR5-DT, RRM2B, 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
    nsv4318515inversion1nstd166human GRCh37.p13 chr8: 75,861,320-132,789,960 , GRCh38.p12 chr8: 74,949,085-131,777,713 , ANXA13, 716 more genes
    nsv4172071copy number variation1nstd166human GRCh37.p13 chr8: 103,253,636-103,273,675 , GRCh38.p12 chr8: 102,241,408-102,261,447 SUMO2P19, UBR5, 1 more genes
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