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Items: 1 to 20 of 509

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5966946insertion1nstd209human GRCh38 chr8: 26,562,514-26,562,514 , GRCh37.p13 chr8: 26,420,030-26,420,030 DPYSL2
    nsv5962933insertion1nstd209human GRCh38 chr8: 26,556,350-26,556,350 , GRCh37.p13 chr8: 26,413,866-26,413,866 DPYSL2
    nsv5920664copy number variation1nstd209human GRCh38 chr8: 26,630,893-26,631,258 , GRCh37.p13 chr8: 26,488,409-26,488,774 DPYSL2
    nsv5916964copy number variation1nstd209human GRCh38 chr8: 26,608,513-26,609,029 , GRCh37.p13 chr8: 26,466,029-26,466,545 DPYSL2
    nsv5912976copy number variation1nstd209human GRCh38 chr8: 26,607,223-26,607,527 , GRCh37.p13 chr8: 26,464,739-26,465,043 DPYSL2
    nsv5911499copy number variation1nstd209human GRCh38 chr8: 26,592,437-26,592,760 , GRCh37.p13 chr8: 26,449,953-26,450,276 DPYSL2
    nsv5861878copy number variation1nstd209human GRCh38 chr8: 26,648,788-26,649,787 , GRCh37.p13 chr8: 26,506,304-26,507,303 DPYSL2
    nsv5707012mobile element insertion1nstd211human GRCh38 chr8: 26,550,381-26,550,381 , GRCh37.p13 chr8: 26,407,897-26,407,897 DPYSL2
    nsv5694420mobile element insertion1nstd211human GRCh38 chr8: 26,557,326-26,557,326 , GRCh37.p13 chr8: 26,414,842-26,414,842 DPYSL2
    nsv5643631insertion1nstd207human GRCh38 chr8: 26,556,349-26,556,349 , GRCh37.p13 chr8: 26,413,865-26,413,865 DPYSL2
    nsv5634071insertion1nstd207human GRCh38 chr8: 26,590,404-26,590,404 , GRCh37.p13 chr8: 26,447,920-26,447,920 DPYSL2
    nsv5633153insertion1nstd207human GRCh38 chr8: 26,590,410-26,590,410 , GRCh37.p13 chr8: 26,447,926-26,447,926 DPYSL2
    nsv5632773insertion1nstd207human GRCh38 chr8: 26,556,220-26,556,220 , GRCh37.p13 chr8: 26,413,736-26,413,736 DPYSL2
    nsv5628540insertion1nstd207human GRCh38 chr8: 26,590,608-26,590,608 , GRCh37.p13 chr8: 26,448,124-26,448,124 DPYSL2
    nsv5626954insertion1nstd207human GRCh38 chr8: 26,556,434-26,556,434 , GRCh37.p13 chr8: 26,413,950-26,413,950 DPYSL2
    nsv5394886mobile element insertion1nstd206human GRCh38 chr8: 26,550,381-26,550,432 , GRCh37.p13 chr8: 26,407,897-26,407,948 DPYSL2
    nsv5308810copy number variation1nstd204human GRCh38.p13 chr8: 26,573,276-26,573,404 , GRCh37.p13 chr8: 26,430,792-26,430,920 DPYSL2
    nsv5249258copy number variation1nstd204human GRCh38.p13 chr8: 26,555,901-26,556,500 , GRCh37.p13 chr8: 26,413,417-26,414,016 DPYSL2
    nsv5200364copy number variation1nstd102humanPathogenic GRCh37 chr8: 176,814-43,396,776 , GRCh38.p12 chr8: 226,814-43,541,633 LOC100130612, XPO7, 770 more genes
    nsv5197798mobile element insertion1nstd203human GRCh38 chr8: 26,595,513-26,595,529 , GRCh37.p13 chr8: 26,453,029-26,453,045 DPYSL2
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