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Items: 1 to 20 of 139

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5711840mobile element insertion1nstd211human GRCh38 chr22: 36,254,213-36,254,213 , GRCh37.p13 chr22: 36,650,259-36,650,259 APOL1
    nsv5702415mobile element insertion2nstd211human GRCh38 chr22: 36,263,063-36,263,063 , GRCh37.p13 chr22: 36,659,109-36,659,109 APOL1
    nsv5562257sequence alteration1nstd206human GRCh38 chr22: 36,225,334-36,268,354 , GRCh37.p13 chr22: 36,621,380-36,664,400 , APOL1, 1 more genes
    nsv5429463mobile element insertion1nstd206human GRCh38 chr22: 36,263,063-36,263,114 , GRCh37.p13 chr22: 36,659,109-36,659,160 APOL1
    nsv5426170mobile element insertion1nstd206human GRCh38 chr22: 36,254,213-36,254,264 , GRCh37.p13 chr22: 36,650,259-36,650,310 APOL1
    nsv5322045copy number variation1nstd204human GRCh38.p13 chr22: 36,216,862-36,318,245 , GRCh37.p13 chr22: 36,612,908-36,714,290 , APOL1, 3 more genes
    nsv5289120copy number variation1nstd204human GRCh38.p13 chr22: 36,218,301-36,317,400 , GRCh37.p13 chr22: 36,614,347-36,713,445 , APOL1, 3 more genes
    nsv5176287mobile element insertion1nstd203human GRCh38 chr22: 36,263,048-36,263,063 , GRCh37.p13 chr22: 36,659,094-36,659,109 APOL1
    nsv5172924mobile element insertion1nstd203human GRCh38 chr22: 36,254,197-36,254,213 , GRCh37.p13 chr22: 36,650,243-36,650,259 APOL1
    nsv5040029copy number variation1nstd200human GRCh38 chr22: 36,212,111-36,265,039 , GRCh37.p13 chr22: 36,608,157-36,661,085 APOL1, APOL2
    nsv5037849copy number variation1nstd200human GRCh38 chr22: 36,262,364-36,262,536 , GRCh37.p13 chr22: 36,658,410-36,658,582 APOL1
    nsv5030440copy number variation1nstd200human GRCh38 chr22: 36,216,892-36,318,221 , GRCh37.p13 chr22: 36,612,938-36,714,266 , MYH9, 3 more genes
    nsv4885595copy number variation1nstd200human GRCh37 chr22: 36,612,938-36,714,266 , GRCh38.p12 chr22: 36,216,892-36,318,221 , APOL1, 3 more genes
    nsv4884197copy number variation1nstd200human GRCh37 chr22: 36,658,410-36,658,582 , GRCh38.p12 chr22: 36,262,364-36,262,536 APOL1
    nsv4729926copy number variation1nstd102humanPathogenic GRCh37 chr22: 16,197,005-51,224,252 , GRCh38.p12 chr22: 16,367,190-50,785,824 FBXO7, GTSE1, 1084 more genes
    nsv4680293copy number variation1nstd189human GRCh37.p13 chr22: 36,556,148-36,749,312 , GRCh38.p12 chr22: 36,160,100-36,353,267 , MYH9, 11 more genes
    nsv4676292copy number variation1nstd102humanPathogenic GRCh37 chr22: 30,654,764-51,197,838 , GRCh38.p12 chr22: 30,258,775-50,759,410 PDXP-DT, PDGFB, 550 more genes
    nsv4627394copy number variation1nstd183human GRCh37 chr22: 36,644,074-36,658,810 , GRCh38.p12 chr22: 36,248,028-36,262,764 APOL1
    nsv4560940sequence alteration1nstd166human GRCh37.p13 chr22: 36,625,047-36,660,212 , GRCh38.p12 chr22: 36,229,001-36,264,166 APOL1, APOL2
    nsv4513405mobile element insertion1nstd166human GRCh37.p13 chr22: 36,659,094-36,659,094 , GRCh38.p12 chr22: 36,263,048-36,263,048 APOL1
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