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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3905566copy number variation1nstd102humanBenign GRCh37 chr14: 50,099,989-50,101,946 , GRCh38.p12 chr14: 49,633,271-49,635,228 DNAAF2
    nsv6938116copy number variation1nstd229human GRCh38 chr14: 49,624,022-49,635,620 , GRCh37.p13 chr14: 50,090,740-50,102,338 DNAAF2
    nsv4213756copy number variation1nstd166human GRCh37.p13 chr14: 50,092,900-50,093,471 , GRCh38.p12 chr14: 49,626,182-49,626,753 DNAAF2
    esv3182823copy number variation1estd209human GRCh37 chr14: 50,099,633-50,099,634 , GRCh38.p12 chr14: 49,632,915-49,632,916 DNAAF2
    esv3182822copy number variation1estd209human GRCh37 chr14: 50,099,417-50,099,418 , GRCh38.p12 chr14: 49,632,699-49,632,700 DNAAF2
    esv3432366copy number variation1estd59human NCBI36 chr14: 49,167,554-49,167,733 , GRCh37.p13 chr14: 50,097,804-50,097,983 , GRCh38.p12 chr14: 49,631,086-49,631,265 DNAAF2
    esv2442041copy number variation1estd197human NCBI36 chr14: 49,169,173-49,169,173 , GRCh37.p13 chr14: 50,099,423-50,099,423 , GRCh38.p12 chr14: 49,632,705-49,632,705 DNAAF2
    esv2394099copy number variation1estd194human NCBI36 chr14: 49,161,405-49,161,409 , GRCh37.p13 chr14: 50,091,655-50,091,659 , GRCh38.p12 chr14: 49,624,937-49,624,941 DNAAF2
    esv1963990copy number variation1estd194human NCBI36 chr14: 49,168,916-49,168,919 , GRCh37.p13 chr14: 50,099,166-50,099,169 , GRCh38.p12 chr14: 49,632,448-49,632,451 DNAAF2
    esv2141421copy number variation1estd194human NCBI36 chr14: 49,169,384-49,169,385 , GRCh37.p13 chr14: 50,099,634-50,099,635 , GRCh38.p12 chr14: 49,632,916-49,632,917 DNAAF2
    esv1462211copy number variation1estd22human NCBI36 chr14: 49,161,404-49,161,408 , GRCh37.p13 chr14: 50,091,654-50,091,658 , GRCh38.p12 chr14: 49,624,936-49,624,940 DNAAF2
    esv1015748copy number variation1estd22human NCBI36 chr14: 49,168,927-49,168,930 , GRCh37.p13 chr14: 50,099,177-50,099,180 , GRCh38.p12 chr14: 49,632,459-49,632,462 DNAAF2
    esv1775269copy number variation1estd22human NCBI36 chr14: 49,163,267-49,163,268 , GRCh37.p13 chr14: 50,093,517-50,093,518 , GRCh38.p12 chr14: 49,626,799-49,626,800 DNAAF2
    esv1565255copy number variation1estd22human NCBI36 chr14: 49,169,393-49,169,394 , GRCh37.p13 chr14: 50,099,643-50,099,644 , GRCh38.p12 chr14: 49,632,925-49,632,926 DNAAF2
    nsv82383copy number variation1nstd6human NCBI35 chr14: 49,168,925-49,168,927 , GRCh37.p13 chr14: 50,099,175-50,099,177 , GRCh38.p12 chr14: 49,632,457-49,632,459 DNAAF2
    nsv80994copy number variation1nstd6human NCBI35 chr14: 49,168,920-49,168,922 , GRCh37.p13 chr14: 50,099,170-50,099,172 , GRCh38.p12 chr14: 49,632,452-49,632,454 DNAAF2
    nsv75373copy number variation1nstd6human NCBI35 chr14: 49,168,916-49,168,918 , GRCh37.p13 chr14: 50,099,166-50,099,168 , GRCh38.p12 chr14: 49,632,448-49,632,450 DNAAF2
    nsv73602copy number variation1nstd6human NCBI35 chr14: 49,168,919-49,168,921 , GRCh37.p13 chr14: 50,099,169-50,099,171 , GRCh38.p12 chr14: 49,632,451-49,632,453 DNAAF2
    nsv86324copy number variation1nstd6human NCBI35 chr14: 49,168,916-49,168,917 , GRCh37.p13 chr14: 50,099,166-50,099,167 , GRCh38.p12 chr14: 49,632,448-49,632,449 DNAAF2
    nsv4501597mobile element insertion1nstd166human GRCh37.p13 chr14: 50,092,133-50,092,133 , GRCh38.p12 chr14: 49,625,415-49,625,415 DNAAF2
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