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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5926628copy number variation1nstd209human GRCh38 chr8: 23,541,085-23,541,219 , GRCh37.p13 chr8: 23,398,598-23,398,732 SLC25A37
    nsv5921867copy number variation1nstd209human GRCh38 chr8: 23,549,706-23,550,345 , GRCh37.p13 chr8: 23,407,219-23,407,858 SLC25A37
    nsv5584262copy number variation1nstd207human GRCh38 chr8: 23,546,553-23,546,609 , GRCh37.p13 chr8: 23,404,066-23,404,122 SLC25A37
    nsv5578836copy number variation1nstd207human GRCh38 chr8: 23,549,706-23,550,345 , GRCh37.p13 chr8: 23,407,219-23,407,858 SLC25A37
    nsv5492121copy number variation1nstd206human GRCh38 chr8: 23,556,477-23,557,137 , GRCh37.p13 chr8: 23,413,990-23,414,650 SLC25A37
    nsv5482247copy number variation1nstd206human GRCh38 chr8: 23,549,710-23,550,346 , GRCh37.p13 chr8: 23,407,223-23,407,859 SLC25A37
    nsv5480362copy number variation1nstd206human GRCh38 chr8: 23,541,087-23,541,220 , GRCh37.p13 chr8: 23,398,600-23,398,733 SLC25A37
    nsv5386268copy number variation2nstd186human GRCh37 chr8: 23,407,223-23,407,859 , GRCh38.p12 chr8: 23,549,710-23,550,346 SLC25A37
    nsv5317475copy number variation1nstd204human GRCh38.p13 chr8: 23,549,710-23,550,346 , GRCh37.p13 chr8: 23,407,223-23,407,859 SLC25A37
    nsv5243900copy number variation1nstd204human GRCh38.p13 chr8: 23,549,421-23,550,870 , GRCh37.p13 chr8: 23,406,934-23,408,383 SLC25A37
    nsv5243626copy number variation1nstd204human GRCh38.p13 chr8: 23,549,701-23,550,300 , GRCh37.p13 chr8: 23,407,214-23,407,813 SLC25A37
    nsv5200364copy number variation1nstd102humanPathogenic GRCh37 chr8: 176,814-43,396,776 , GRCh38.p12 chr8: 226,814-43,541,633 LOC100130612, XPO7, 770 more genes
    nsv4959697copy number variation1nstd200human GRCh38 chr8: 23,566,184-23,569,526 , GRCh37.p13 chr8: 23,423,697-23,427,039 SLC25A37
    nsv4959696copy number variation1nstd200human GRCh38 chr8: 23,549,710-23,550,346 , GRCh37.p13 chr8: 23,407,223-23,407,859 SLC25A37
    nsv4821500copy number variation1nstd200human GRCh37 chr8: 23,407,223-23,407,859 , GRCh38.p12 chr8: 23,549,710-23,550,346 SLC25A37
    nsv4739081copy number variation1nstd199human GRCh37 chr8: 23,407,218-23,407,858 , GRCh38.p12 chr8: 23,549,705-23,550,345 SLC25A37
    nsv4728911copy number variation1nstd102humanLikely pathogenic GRCh37 chr8: 12,528,482-29,886,483 , GRCh38.p12 chr8: 12,670,973-30,028,967 NAT1, NAT2, 272 more genes
    nsv4672603copy number variation1nstd186human GRCh37 chr8: 23,406,986-23,407,907 , GRCh38.p12 chr8: 23,549,473-23,550,394 SLC25A37
    nsv4639804copy number variation1nstd186human GRCh37 chr8: 23,407,223-23,407,712 , GRCh38.p12 chr8: 23,549,710-23,550,199 SLC25A37
    nsv4637477copy number variation1nstd186human GRCh37 chr8: 23,407,217-23,407,862 , GRCh38.p12 chr8: 23,549,704-23,550,349 SLC25A37
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