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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5910174copy number variation1nstd209human GRCh38 chr9: 136,687,516-136,687,567 , GRCh37.p13 chr9: 139,581,968-139,582,019 AGPAT2
    nsv5631855insertion1nstd207human GRCh38 chr9: 136,675,429-136,675,429 , GRCh37.p13 chr9: 139,569,881-139,569,881 AGPAT2
    nsv5627475insertion1nstd207human GRCh38 chr9: 136,675,317-136,675,317 , GRCh37.p13 chr9: 139,569,769-139,569,769 AGPAT2
    nsv5627076insertion1nstd207human GRCh38 chr9: 136,675,470-136,675,470 , GRCh37.p13 chr9: 139,569,922-139,569,922 AGPAT2
    nsv5626462insertion1nstd207human GRCh38 chr9: 136,675,388-136,675,388 , GRCh37.p13 chr9: 139,569,840-139,569,840 AGPAT2
    nsv5591356copy number variation1nstd207human GRCh38 chr9: 136,675,444-136,675,525 , GRCh37.p13 chr9: 139,569,896-139,569,977 AGPAT2
    nsv5587827copy number variation1nstd207human GRCh38 chr9: 136,671,235-136,671,286 , GRCh37.p13 chr9: 139,565,687-139,565,738 EGFL7, AGPAT2
    nsv5564455copy number variation1nstd102humanUncertain significance GRCh37 chr9: 139,297,240-139,572,028 , GRCh38.p12 chr9: 136,402,788-136,677,576 LOC105376325, NOTCH1, 14 more genes
    nsv5489359copy number variation1nstd206human GRCh38 chr9: 136,672,589-136,673,269 , GRCh37.p13 chr9: 139,567,041-139,567,721 AGPAT2, EGFL7
    nsv5476368copy number variation1nstd206human GRCh38 chr9: 136,679,870-136,679,950 , GRCh37.p13 chr9: 139,574,322-139,574,402 AGPAT2
    nsv5381762copy number variation1nstd102humanPathogenic GRCh37 chr9: 139,284,464-141,018,984 , GRCh38.p12 chr9: 136,390,012-138,124,532 ARRDC1, SETP5, 101 more genes
    nsv5344618translocation1nstd200human GRCh37 chr9: 139,569,960-139,569,960 , GRCh37 chr9: 139,569,836-139,569,836 , GRCh38.p12 chr9: 136,675,384-136,675,384 , GRCh38.p12 chr9: 136,675,508-136,675,508 AGPAT2
    nsv5248645copy number variation1nstd204human GRCh38.p13 chr9: 136,668,964-136,672,263 , GRCh37.p13 chr9: 139,563,416-139,566,715 MIR126, AGPAT2, 1 more genes
    nsv5246206copy number variation1nstd204human GRCh38.p13 chr9: 136,043,001-136,766,200 , GRCh37.p13 chr9: 138,934,847-139,660,652 MIR4674, TMEM250, 37 more genes
    nsv5242695copy number variation1nstd204human GRCh38.p13 chr9: 136,672,990-136,682,707 , GRCh37.p13 chr9: 139,567,442-139,577,159 AGPAT2, EGFL7
    nsv4985870copy number variation1nstd200human GRCh38 chr9: 136,632,294-136,850,190 , GRCh37.p13 chr9: 139,526,746-139,744,642 CCDC183, PHPT1, 25 more genes
    nsv4985869copy number variation1nstd200human GRCh38 chr9: 136,591,087-136,947,348 , GRCh37.p13 chr9: 139,485,539-139,841,800 LOC102724193, AJM1, 34 more genes
    nsv4985868copy number variation1nstd200human GRCh38 chr9: 136,528,503-136,809,431 , GRCh37.p13 chr9: 139,422,955-139,703,883 LCN6, DIPK1B, 25 more genes
    nsv4973369copy number variation1nstd200human GRCh38 chr9: 136,676,050-136,677,087 , GRCh37.p13 chr9: 139,570,502-139,571,539 AGPAT2
    nsv4973368copy number variation1nstd200human GRCh38 chr9: 136,672,589-136,673,269 , GRCh37.p13 chr9: 139,567,041-139,567,721 EGFL7, AGPAT2
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