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Items: 1 to 20 of 162

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5947868copy number variation1nstd209human GRCh38 chr22: 36,240,404-36,241,015 , GRCh37.p13 chr22: 36,636,450-36,637,061 APOL2
    nsv5562257sequence alteration1nstd206human GRCh38 chr22: 36,225,334-36,268,354 , GRCh37.p13 chr22: 36,621,380-36,664,400 , APOL1, 1 more genes
    nsv5546421copy number variation1nstd206human GRCh38 chr22: 36,239,332-36,239,900 , GRCh37.p13 chr22: 36,635,378-36,635,946 APOL2
    nsv5540224copy number variation1nstd206human GRCh38 chr22: 36,200,337-36,233,797 , GRCh37.p13 chr22: 36,596,383-36,629,843 APOL2, APOL4
    nsv5375689translocation1nstd200human GRCh38 chr22: 36,225,334-36,225,334 , GRCh38 chr22: 36,268,305-36,268,305 , GRCh37.p13 chr22: 36,664,351-36,664,351 , GRCh37.p13 chr22: 36,621,380-36,621,380 , APOL2
    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
    nsv5289549copy number variation1nstd204human GRCh38.p13 chr22: 36,218,470-36,248,072 , GRCh37.p13 chr22: 36,614,516-36,644,118 APOL2
    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
    nsv5040029copy number variation1nstd200human GRCh38 chr22: 36,212,111-36,265,039 , GRCh37.p13 chr22: 36,608,157-36,661,085 APOL1, APOL2
    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
    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
    nsv4560940sequence alteration1nstd166human GRCh37.p13 chr22: 36,625,047-36,660,212 , GRCh38.p12 chr22: 36,229,001-36,264,166 APOL1, APOL2
    nsv4457771copy number variation1nstd102humanPathogenic GRCh37 chr22: 16,888,899-51,197,838 , GRCh38.p12 chr22: 16,408,173-50,759,410 IGLV3-27, XKR3, 1082 more genes
    nsv4414926copy number variation1nstd174human GRCh37 chr22: 36,614,298-36,715,837 , GRCh38.p12 chr22: 36,218,252-36,319,792 , APOL1, 3 more genes
    nsv4371575copy number variation1nstd173human GRCh37 chr22: 36,614,413-36,716,248 , GRCh38.p12 chr22: 36,218,367-36,320,203 , MYH9, 3 more genes
    nsv4339422sequence alteration1nstd166human GRCh37.p13 chr22: 36,473,074-37,010,208 , GRCh38.p12 chr22: 36,077,026-36,614,161 , APOL2, 22 more genes
    nsv4339416sequence alteration1nstd166human GRCh37.p13 chr22: 36,621,382-36,664,390 , GRCh38.p12 chr22: 36,225,336-36,268,344 , APOL1, 1 more genes
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