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Items: 1 to 20 of 261

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5717892mobile element insertion1nstd211human GRCh38 chr9: 113,478,103-113,478,103 , GRCh37.p13 chr9: 116,240,383-116,240,383 RGS3
    nsv5701053mobile element insertion1nstd211human GRCh38 chr9: 113,498,219-113,498,219 , GRCh37.p13 chr9: 116,260,499-116,260,499 RGS3
    nsv5638046insertion1nstd207human GRCh38 chr9: 113,453,315-113,453,315 , GRCh37.p13 chr9: 116,215,595-116,215,595 RGS3
    nsv5626025insertion1nstd207human GRCh38 chr9: 113,447,319-113,447,319 , GRCh37.p13 chr9: 116,209,599-116,209,599 RGS3
    nsv5602702copy number variation1nstd207human GRCh38 chr9: 113,453,494-113,453,664 , GRCh37.p13 chr9: 116,215,774-116,215,944 RGS3
    nsv5593052copy number variation1nstd207human GRCh38 chr9: 113,453,291-113,453,482 , GRCh37.p13 chr9: 116,215,571-116,215,762 RGS3
    nsv5592459copy number variation1nstd207human GRCh38 chr9: 113,453,339-113,453,410 , GRCh37.p13 chr9: 116,215,619-116,215,690 RGS3
    nsv5592158copy number variation1nstd207human GRCh38 chr9: 113,453,110-113,453,535 , GRCh37.p13 chr9: 116,215,390-116,215,815 RGS3
    nsv5476670copy number variation1nstd206human GRCh38 chr9: 113,452,903-113,452,960 , GRCh37.p13 chr9: 116,215,183-116,215,240 RGS3
    nsv5404717mobile element insertion1nstd206human GRCh38 chr9: 113,498,219-113,498,270 , GRCh37.p13 chr9: 116,260,499-116,260,550 RGS3
    nsv5373005translocation1nstd200human GRCh38 chr9: 113,453,846-113,453,846 , GRCh38 chr9: 113,452,919-113,452,919 , GRCh37.p13 chr9: 116,215,199-116,215,199 , GRCh37.p13 chr9: 116,216,126-116,216,126 RGS3
    nsv5199188mobile element insertion1nstd203human GRCh38 chr9: 113,478,098-113,478,103 , GRCh37.p13 chr9: 116,240,378-116,240,383 RGS3
    nsv5138710mobile element insertion1nstd203human GRCh38 chr9: 113,546,457-113,546,473 , GRCh37.p13 chr9: 116,308,737-116,308,753 RGS3
    nsv5127213mobile element insertion1nstd203human GRCh38 chr9: 113,445,569-113,445,582 , GRCh37.p13 chr9: 116,207,849-116,207,862 RGS3
    nsv5125604mobile element insertion1nstd203human GRCh38 chr9: 113,445,566-113,445,577 , GRCh37.p13 chr9: 116,207,846-116,207,857 RGS3
    nsv5040732inversion1nstd200human GRCh38 chr9: 100,673,006-127,581,711 , GRCh37.p13 chr9: 103,435,288-130,343,990 , LOC105379839, 440 more genes
    nsv4983271copy number variation1nstd200human GRCh38 chr9: 113,554,267-113,555,473 , GRCh37.p13 chr9: 116,316,547-116,317,753 RGS3
    nsv4983270copy number variation1nstd200human GRCh38 chr9: 113,484,164-113,489,969 , GRCh37.p13 chr9: 116,246,444-116,252,249 RGS3
    nsv4983269copy number variation1nstd200human GRCh38 chr9: 113,479,879-113,486,686 , GRCh37.p13 chr9: 116,242,159-116,248,966 RGS3
    nsv4983268copy number variation1nstd200human GRCh38 chr9: 113,444,945-113,445,002 , GRCh37.p13 chr9: 116,207,225-116,207,282 RGS3
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