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 1166

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5966349insertion1nstd209human GRCh38 chr6: 152,139,717-152,139,717 , GRCh37.p13 chr6: 152,460,852-152,460,852 SYNE1
    nsv5960891insertion1nstd209human GRCh38 chr6: 152,536,398-152,536,398 , GRCh37.p13 chr6: 152,857,533-152,857,533 SYNE1
    nsv5948583insertion1nstd209human GRCh38 chr6: 152,179,655-152,179,655 , GRCh37.p13 chr6: 152,500,790-152,500,790 SYNE1
    nsv5902844copy number variation1nstd209human GRCh38 chr6: 152,140,778-152,141,500 , GRCh37.p13 chr6: 152,461,913-152,462,635 SYNE1
    nsv5896334copy number variation1nstd209human GRCh38 chr6: 152,135,853-152,135,936 , GRCh37.p13 chr6: 152,456,988-152,457,071 SYNE1
    nsv5893092copy number variation1nstd209human GRCh38 chr6: 152,536,381-152,536,445 , GRCh37.p13 chr6: 152,857,516-152,857,580 SYNE1
    nsv5892280copy number variation1nstd209human GRCh38 chr6: 152,133,854-152,134,000 , GRCh37.p13 chr6: 152,454,989-152,455,135 SYNE1
    nsv5889606copy number variation1nstd209human GRCh38 chr6: 152,291,114-152,291,237 , GRCh37.p13 chr6: 152,612,249-152,612,372 SYNE1
    nsv5724280mobile element insertion2nstd211human GRCh38 chr6: 152,153,449-152,153,449 , GRCh37.p13 chr6: 152,474,584-152,474,584 SYNE1
    nsv5720830mobile element insertion2nstd211human GRCh38 chr6: 152,479,901-152,479,901 , GRCh37.p13 chr6: 152,801,036-152,801,036 SYNE1
    nsv5717916mobile element insertion1nstd211human GRCh38 chr6: 152,589,654-152,589,654 , GRCh37.p13 chr6: 152,910,789-152,910,789 SYNE1
    nsv5692979mobile element insertion1nstd211human GRCh38 chr6: 152,566,450-152,566,450 , GRCh37.p13 chr6: 152,887,585-152,887,585 SYNE1
    nsv5691363mobile element insertion1nstd211human GRCh38 chr6: 152,534,706-152,534,706 , GRCh37.p13 chr6: 152,855,841-152,855,841 SYNE1
    nsv5690854mobile element insertion1nstd211human GRCh38 chr6: 152,222,522-152,222,522 , GRCh37.p13 chr6: 152,543,657-152,543,657 SYNE1
    nsv5687774mobile element insertion1nstd211human GRCh38 chr6: 152,282,090-152,282,090 , GRCh37.p13 chr6: 152,603,225-152,603,225 SYNE1
    nsv5684697mobile element insertion1nstd211human GRCh38 chr6: 152,516,137-152,516,137 , GRCh37.p13 chr6: 152,837,272-152,837,272 SYNE1
    nsv5684618mobile element insertion2nstd211human GRCh38 chr6: 152,188,985-152,188,985 , GRCh37.p13 chr6: 152,510,120-152,510,120 SYNE1
    nsv5679304mobile element insertion1nstd211human GRCh38 chr6: 152,333,365-152,333,365 , GRCh37.p13 chr6: 152,654,500-152,654,500 SYNE1
    nsv5678261mobile element insertion2nstd211human GRCh38 chr6: 152,237,824-152,237,824 , GRCh37.p13 chr6: 152,558,959-152,558,959 SYNE1
    nsv5675210mobile element insertion1nstd211human GRCh38 chr6: 152,605,114-152,605,114 , GRCh37.p13 chr6: 152,926,249-152,926,249 SYNE1
    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