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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5965347insertion1nstd209human GRCh38 chr10: 12,237,433-12,237,433 , GRCh37.p13 chr10: 12,279,432-12,279,432 CDC123
    nsv5921237copy number variation1nstd209human GRCh38 chr10: 12,246,931-12,247,336 , GRCh37.p13 chr10: 12,288,930-12,289,335 CDC123
    nsv5919443copy number variation1nstd209human GRCh38 chr10: 12,250,878-12,251,768 , GRCh37.p13 chr10: 12,292,877-12,293,767 CDC123
    nsv5723995mobile element insertion1nstd211human GRCh38 chr10: 12,250,581-12,250,581 , GRCh37.p13 chr10: 12,292,580-12,292,580 CDC123
    nsv5708404mobile element insertion2nstd211human GRCh38 chr10: 12,211,315-12,211,315 , GRCh37.p13 chr10: 12,253,314-12,253,314 CDC123
    nsv5642916insertion1nstd207human GRCh38 chr10: 12,198,438-12,198,438 , GRCh37.p13 chr10: 12,240,437-12,240,437 CDC123
    nsv5642541insertion1nstd207human GRCh38 chr10: 12,237,433-12,237,433 , GRCh37.p13 chr10: 12,279,432-12,279,432 CDC123
    nsv5631890insertion1nstd207human GRCh38 chr10: 12,247,194-12,247,194 , GRCh37.p13 chr10: 12,289,193-12,289,193 CDC123
    nsv5594405copy number variation1nstd207human GRCh38 chr10: 12,247,085-12,247,354 , GRCh37.p13 chr10: 12,289,084-12,289,353 CDC123
    nsv5551863insertion1nstd206human GRCh38 chr10: 12,237,433-12,237,433 , GRCh37.p13 chr10: 12,279,432-12,279,432 CDC123
    nsv5492685copy number variation1nstd206human GRCh38 chr10: 12,246,957-12,247,446 , GRCh37.p13 chr10: 12,288,956-12,289,445 CDC123
    nsv5490502copy number variation1nstd206human GRCh38 chr10: 12,201,489-12,201,544 , GRCh37.p13 chr10: 12,243,488-12,243,543 CDC123
    nsv5490332copy number variation1nstd206human GRCh38 chr10: 12,200,653-12,828,405 , GRCh37.p13 chr10: 12,242,652-12,870,404 CDC123, CAMK1D, 6 more genes
    nsv5409975mobile element insertion1nstd206human GRCh38 chr10: 12,211,315-12,211,366 , GRCh37.p13 chr10: 12,253,314-12,253,365 CDC123
    nsv5389116copy number variation1nstd186human GRCh37 chr10: 12,288,907-12,289,261 , GRCh38.p12 chr10: 12,246,908-12,247,262 CDC123
    nsv5388519copy number variation1nstd186human GRCh37 chr10: 12,288,965-12,289,511 , GRCh38.p12 chr10: 12,246,966-12,247,512 CDC123
    nsv5387659copy number variation1nstd186human GRCh37 chr10: 12,289,115-12,289,352 , GRCh38.p12 chr10: 12,247,116-12,247,353 CDC123
    nsv5387601copy number variation1nstd186human GRCh37 chr10: 12,289,196-12,289,503 , GRCh38.p12 chr10: 12,247,197-12,247,504 CDC123
    nsv5381768copy number variation1nstd102humanPathogenic GRCh37 chr10: 9,137,489-17,227,168 , GRCh38.p12 chr10: 9,095,526-17,185,169 PROSER2, C1QL3, 110 more genes
    nsv5364750translocation1nstd200human GRCh38 chr10: 12,214,149-12,214,149 , GRCh38 chr11: 85,636,506-85,636,506 , GRCh37.p13 chr10: 12,256,148-12,256,148 , GRCh37.p13 chr11: 85,347,550-85,347,550 TMEM126B, CDC123
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