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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
    nsv5969270insertion1nstd209human GRCh38 chr22: 36,165,240-36,165,240 , GRCh37.p13 chr22: 36,561,288-36,561,288 APOL3
    nsv5961471copy number variation1nstd209human GRCh38 chr22: 36,145,992-36,195,742 , GRCh37.p13 chr22: 36,542,040-36,591,788 APOL4, APOL3, 6 more genes
    nsv5730955mobile element insertion1nstd211human GRCh38 chr22: 36,160,810-36,160,810 , GRCh37.p13 chr22: 36,556,858-36,556,858 APOL3
    nsv5710303mobile element insertion2nstd211human GRCh38 chr22: 36,165,254-36,165,254 , GRCh37.p13 chr22: 36,561,302-36,561,302 APOL3
    nsv5665430insertion1nstd207human GRCh38 chr22: 36,165,240-36,165,240 , GRCh37.p13 chr22: 36,561,288-36,561,288 APOL3
    nsv5554274mobile element insertion1nstd206human GRCh38 chr22: 36,160,825-36,160,861 , GRCh37.p13 chr22: 36,556,873-36,556,909 APOL3
    nsv5544766copy number variation1nstd206human GRCh38 chr22: 36,137,564-36,187,564 , GRCh37.p13 chr22: 36,533,612-36,583,612 APOL4, APOL3, 6 more genes
    nsv5417931mobile element insertion1nstd206human GRCh38 chr22: 36,165,240-36,165,240 , GRCh37.p13 chr22: 36,561,288-36,561,288 APOL3
    nsv5366069translocation1nstd200human GRCh38 chr20: 30,377,207-30,377,207 , GRCh38 chr22: 36,160,825-36,160,825 , GRCh37.p13 chr20: 29,611,883-29,611,883 , GRCh37.p13 chr22: 36,556,873-36,556,873 APOL3, FRG1BP
    nsv5288086copy number variation1nstd204human GRCh38.p13 chr22: 36,148,201-36,149,652 , GRCh37.p13 chr22: 36,544,249-36,545,700 APOL3
    nsv5167527mobile element insertion1nstd203human GRCh38 chr22: 36,165,240-36,165,250 , GRCh37.p13 chr22: 36,561,288-36,561,298 APOL3
    nsv5038565copy number variation1nstd200human GRCh38 chr22: 36,130,233-36,143,259 , GRCh37.p13 chr22: 36,526,281-36,539,307 , APOL3
    nsv5038365copy number variation1nstd200human GRCh38 chr22: 36,150,867-36,159,575 , GRCh37.p13 chr22: 36,546,915-36,555,623 APOL3
    nsv4883273copy number variation1nstd200human GRCh37 chr22: 36,546,915-36,555,623 , GRCh38.p12 chr22: 36,150,867-36,159,575 APOL3
    nsv4871796copy number variation1nstd200human GRCh37 chr22: 36,526,281-36,539,307 , GRCh38.p12 chr22: 36,130,233-36,143,259 , APOL3
    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
    nsv4720342insertion1nstd186human GRCh37 chr22: 36,561,288-36,561,288 , GRCh38.p12 chr22: 36,165,240-36,165,240 APOL3
    nsv4691366mobile element insertion2nstd186human GRCh37 chr22: 36,561,288-36,561,288 , GRCh38.p12 chr22: 36,165,240-36,165,240 APOL3
    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
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