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Items: 1 to 20 of 170

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5971913inversion1nstd209human GRCh38 chr3: 63,121,698-63,123,594 , GRCh37.p13 chr3: 63,107,374-63,109,270 LINC00698
    nsv5968863inversion1nstd209human GRCh38 chr3: 63,118,635-63,120,043 , GRCh37.p13 chr3: 63,104,311-63,105,719 LINC00698
    nsv5836652copy number variation1nstd209human GRCh38 chr3: 63,118,618-63,121,717 , GRCh37.p13 chr3: 63,104,294-63,107,393 LINC00698
    nsv5621025insertion1nstd207human GRCh38 chr3: 63,118,642-63,118,642 , GRCh37.p13 chr3: 63,104,318-63,104,318 LINC00698
    nsv5575353copy number variation1nstd207human GRCh38 chr3: 63,118,651-63,121,694 , GRCh37.p13 chr3: 63,104,327-63,107,370 LINC00698
    nsv5559545sequence alteration1nstd206human GRCh38 chr3: 63,118,637-63,121,698 , GRCh37.p13 chr3: 63,104,313-63,107,374 LINC00698
    nsv5447736copy number variation1nstd206human GRCh38 chr3: 63,118,722-63,121,592 , GRCh37.p13 chr3: 63,104,398-63,107,268 LINC00698
    nsv5442135copy number variation1nstd206human GRCh38 chr3: 63,104,457-63,104,540 , GRCh37.p13 chr3: 63,090,133-63,090,216 LINC00698
    nsv5436808copy number variation1nstd206human GRCh38 chr3: 62,956,000-63,216,000 , GRCh37.p13 chr3: 62,941,675-63,201,676 , SYNPR, 3 more genes
    nsv5361630translocation1nstd200human GRCh38 chr3: 63,121,699-63,121,699 , GRCh38 chr3: 63,119,802-63,119,802 , GRCh37.p13 chr3: 63,105,478-63,105,478 , GRCh37.p13 chr3: 63,107,375-63,107,375 LINC00698
    nsv5361629translocation1nstd200human GRCh38 chr3: 63,118,637-63,118,637 , GRCh38 chr3: 63,120,044-63,120,044 , GRCh37.p13 chr3: 63,104,313-63,104,313 , GRCh37.p13 chr3: 63,105,720-63,105,720 LINC00698
    nsv5344521translocation1nstd200human GRCh37 chr3: 63,104,313-63,104,313 , GRCh37 chr3: 63,105,720-63,105,720 , GRCh38.p12 chr3: 63,118,637-63,118,637 , GRCh38.p12 chr3: 63,120,044-63,120,044 LINC00698
    nsv5340057translocation1nstd200human GRCh37 chr3: 63,105,478-63,105,478 , GRCh37 chr3: 63,107,375-63,107,375 , GRCh38.p12 chr3: 63,119,802-63,119,802 , GRCh38.p12 chr3: 63,121,699-63,121,699 LINC00698
    nsv5030280inversion1nstd200human GRCh38 chr3: 3,432,416-77,775,308 , GRCh37.p13 chr3: 3,474,100-77,824,459 , BHLHE40, 1198 more genes
    nsv4918593copy number variation1nstd200human GRCh38 chr3: 63,118,633-63,121,701 , GRCh37.p13 chr3: 63,104,309-63,107,377 LINC00698
    nsv4888770inversion1nstd200human GRCh37 chr3: 3,474,100-77,824,459 , GRCh38.p12 chr3: 3,432,416-77,775,308 , ATRIP, 1198 more genes
    nsv4877503inversion1nstd200human GRCh37 chr3: 24,885,632-100,711,157 , GRCh38.p12 chr3: 24,844,141-100,992,313 , LINC00692, 1088 more genes
    nsv4790963copy number variation1nstd200human GRCh37 chr3: 63,104,282-63,107,404 , GRCh38.p12 chr3: 63,118,606-63,121,728 LINC00698
    nsv4728543copy number variation1nstd102humanUncertain significance GRCh37 chr3: 62,894,703-63,320,384 , GRCh38.p12 chr3: 62,909,028-63,334,708 UBL5P3, SYNPR, 3 more genes
    nsv4685651copy number variation1nstd102humanUncertain significance GRCh37 chr3: 62,899,731-63,601,696 , GRCh38.p12 chr3: 62,914,056-63,616,020 KRT8P35, RPS10P10, 5 more genes
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