U.S. flag

An official website of the United States government

Format
Items per page

Send to:

Choose Destination

Links from Gene

Items: 1 to 20 of 793

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5979455inversion1nstd209human GRCh38 chr6: 77,770,273-77,777,192 , GRCh37.p13 chr6: 78,479,990-78,486,909 MEI4
    nsv5962873insertion1nstd209human GRCh38 chr6: 77,841,331-77,841,331 , GRCh37.p13 chr6: 78,551,048-78,551,048 MEI4
    nsv5960441insertion1nstd209human GRCh38 chr6: 77,654,537-77,654,537 , GRCh37.p13 chr6: 78,364,254-78,364,254 MEI4
    nsv5952307insertion1nstd209human GRCh38 chr6: 77,707,036-77,707,036 , GRCh37.p13 chr6: 78,416,753-78,416,753 MEI4
    nsv5950167insertion1nstd209human GRCh38 chr6: 77,883,724-77,883,724 , GRCh37.p13 chr6: 78,593,441-78,593,441 MEI4
    nsv5905569copy number variation1nstd209human GRCh38 chr6: 77,771,949-77,774,668 , GRCh37.p13 chr6: 78,481,666-78,484,385 MEI4
    nsv5903658copy number variation1nstd209human GRCh38 chr6: 77,765,209-77,765,818 , GRCh37.p13 chr6: 78,474,926-78,475,535 MEI4
    nsv5900247copy number variation1nstd209human GRCh38 chr6: 77,665,462-77,665,522 , GRCh37.p13 chr6: 78,375,179-78,375,239 MEI4
    nsv5894258copy number variation1nstd209human GRCh38 chr6: 77,716,937-77,726,364 , GRCh37.p13 chr6: 78,426,654-78,436,081 MEI4
    nsv5892476copy number variation1nstd209human GRCh38 chr6: 77,772,000-77,775,605 , GRCh37.p13 chr6: 78,481,717-78,485,322 MEI4
    nsv5892162copy number variation1nstd209human GRCh38 chr6: 77,774,742-77,775,630 , GRCh37.p13 chr6: 78,484,459-78,485,347 MEI4
    nsv5891037copy number variation1nstd209human GRCh38 chr6: 77,730,801-77,736,962 , GRCh37.p13 chr6: 78,440,518-78,446,679 MEI4
    nsv5888409copy number variation1nstd209human GRCh38 chr6: 77,885,013-77,885,388 , GRCh37.p13 chr6: 78,594,730-78,595,105 MEI4
    nsv5846095copy number variation1nstd209human GRCh38 chr6: 77,771,064-77,775,663 , GRCh37.p13 chr6: 78,480,781-78,485,380 MEI4
    nsv5845974copy number variation1nstd209human GRCh38 chr6: 77,697,574-77,719,142 , GRCh37.p13 chr6: 78,407,291-78,428,859 MEI4
    nsv5845720copy number variation1nstd209human GRCh38 chr6: 77,730,370-77,734,637 , GRCh37.p13 chr6: 78,440,087-78,444,354 MEI4
    nsv5845451copy number variation1nstd209human GRCh38 chr6: 77,734,028-77,736,615 , GRCh37.p13 chr6: 78,443,745-78,446,332 MEI4
    nsv5845450copy number variation1nstd209human GRCh38 chr6: 77,726,343-77,733,643 , GRCh37.p13 chr6: 78,436,060-78,443,360 MEI4
    nsv5729228mobile element insertion2nstd211human GRCh38 chr6: 77,805,862-77,805,862 , GRCh37.p13 chr6: 78,515,579-78,515,579 MEI4
    nsv5728716mobile element insertion1nstd211human GRCh38 chr6: 77,766,325-77,766,325 , GRCh37.p13 chr6: 78,476,042-78,476,042 MEI4
    Format
    Items per page

    Send to:

    Choose Destination

    Supplemental Content

    Filters: Manage Filters

    Find related data

    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