U.S. flag

An official website of the United States government

Format
Items per page

Send to:

Choose Destination

Search results

Items: 1 to 20 of 746

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3872190copy number variation1nstd102humanBenign GRCh37 chr4: 7,971,604-7,980,298 , GRCh38.p12 chr4: 7,969,877-7,978,571 ABLIM2
    nsv3886851copy number variation1nstd102humanBenign GRCh37 chr4: 7,971,604-7,974,666 , GRCh38.p12 chr4: 7,969,877-7,972,939 ABLIM2
    nsv3874669copy number variation1nstd102humanBenign GRCh37 chr4: 7,971,604-7,974,491 , GRCh38.p12 chr4: 7,969,877-7,972,764 ABLIM2
    esv4004745copy number variation1estd231human GRCh37 chr4: 7,995,794-7,996,893 , GRCh38.p12 chr4: 7,994,067-7,995,166 ABLIM2
    nsv6729556copy number variation1nstd229human GRCh38 chr4: 8,104,628-8,149,382 , GRCh37.p13 chr4: 8,106,355-8,151,109 ABLIM2
    nsv6727265copy number variation1nstd229human GRCh38 chr4: 7,987,934-7,999,120 , GRCh37.p13 chr4: 7,989,661-8,000,847 ABLIM2
    nsv6732778copy number variation1nstd229human GRCh38 chr4: 8,116,240-8,123,781 , GRCh37.p13 chr4: 8,117,967-8,125,508 ABLIM2
    nsv6737444copy number variation1nstd229human GRCh38 chr4: 8,021,365-8,027,209 , GRCh37.p13 chr4: 8,023,092-8,028,936 ABLIM2
    nsv6731511copy number variation1nstd229human GRCh38 chr4: 7,968,565-7,973,261 , GRCh37.p13 chr4: 7,970,292-7,974,988 ABLIM2
    nsv6727654copy number variation1nstd229human GRCh38 chr4: 7,987,514-7,992,160 , GRCh37.p13 chr4: 7,989,241-7,993,887 ABLIM2
    nsv6728995copy number variation1nstd229human GRCh38 chr4: 7,969,023-7,973,441 , GRCh37.p13 chr4: 7,970,750-7,975,168 ABLIM2
    nsv6736723copy number variation1nstd229human GRCh38 chr4: 7,969,037-7,973,342 , GRCh37.p13 chr4: 7,970,764-7,975,069 ABLIM2
    nsv6718473copy number variation1nstd229human GRCh38 chr4: 8,048,737-8,052,394 , GRCh37.p13 chr4: 8,050,464-8,054,121 ABLIM2
    nsv6736313copy number variation1nstd229human GRCh38 chr4: 7,969,001-7,972,300 , GRCh37.p13 chr4: 7,970,728-7,974,027 ABLIM2
    nsv6720747copy number variation1nstd229human GRCh38 chr4: 8,068,831-8,071,981 , GRCh37.p13 chr4: 8,070,558-8,073,708 ABLIM2
    nsv6721812copy number variation1nstd229human GRCh38 chr4: 8,093,636-8,096,665 , GRCh37.p13 chr4: 8,095,363-8,098,392 ABLIM2
    nsv6718530copy number variation1nstd229human GRCh38 chr4: 8,120,263-8,122,926 , GRCh37.p13 chr4: 8,121,990-8,124,653 ABLIM2
    nsv6724622copy number variation1nstd229human GRCh38 chr4: 8,000,011-8,000,886 , GRCh37.p13 chr4: 8,001,738-8,002,613 ABLIM2
    nsv6369535copy number variation1nstd223human GRCh38 chr4: 7,987,503-7,992,159 , GRCh37.p13 chr4: 7,989,230-7,993,886 ABLIM2
    nsv6368087copy number variation1nstd223human GRCh38 chr4: 7,969,016-7,973,344 , GRCh37.p13 chr4: 7,970,743-7,975,071 ABLIM2
    Format
    Items per page

    Send to:

    Choose Destination

    Supplemental Content

    Filters: Manage Filters

    Find related data

    Search details

    See more...

    Recent activity

    Clear Turn Off Turn On

    Your browsing activity is empty.

    Activity recording is turned off.

    Turn recording back on

    See more...
    You are here: NCBI > Variation > Database of Genomic Structural Variation (dbVar)
    Support Center