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 722

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5975786insertion1nstd209human GRCh38 chr12: 116,277,338-116,277,338 , GRCh37.p13 chr12: 116,715,143-116,715,143 MED13L
    nsv5968474insertion1nstd209human GRCh38 chr12: 116,145,279-116,145,279 , GRCh37.p13 chr12: 116,583,084-116,583,084 MED13L
    nsv5947468copy number variation1nstd209human GRCh38 chr12: 115,992,401-115,992,559 , GRCh37.p13 chr12: 116,430,206-116,430,364 MED13L
    nsv5944074copy number variation1nstd209human GRCh38 chr12: 116,165,141-116,165,294 , GRCh37.p13 chr12: 116,602,946-116,603,099 MED13L
    nsv5934700copy number variation1nstd209human GRCh38 chr12: 116,088,668-116,090,681 , GRCh37.p13 chr12: 116,526,473-116,528,486 MED13L
    nsv5861381copy number variation2nstd209human GRCh38 chr12: 116,088,648-116,090,647 , GRCh37.p13 chr12: 116,526,453-116,528,452 MED13L
    nsv5854016copy number variation1nstd209human GRCh38 chr12: 115,966,121-115,967,258 , GRCh37.p13 chr12: 116,403,926-116,405,063 MED13L
    nsv5848227copy number variation1nstd209human GRCh38 chr12: 116,268,735-116,271,681 , GRCh37.p13 chr12: 116,706,540-116,709,486 MED13L
    nsv5716803mobile element insertion2nstd211human GRCh38 chr12: 116,100,314-116,100,314 , GRCh37.p13 chr12: 116,538,119-116,538,119 MED13L
    nsv5714682mobile element insertion1nstd211human GRCh38 chr12: 115,979,286-115,979,286 , GRCh37.p13 chr12: 116,417,091-116,417,091 MED13L
    nsv5651192insertion1nstd207human GRCh38 chr12: 116,277,345-116,277,345 , GRCh37.p13 chr12: 116,715,150-116,715,150 MED13L
    nsv5646467insertion1nstd207human GRCh38 chr12: 116,124,148-116,124,148 , GRCh37.p13 chr12: 116,561,953-116,561,953 MED13L
    nsv5558798mobile element insertion1nstd206human GRCh38 chr12: 115,979,286-115,979,337 , GRCh37.p13 chr12: 116,417,091-116,417,142 MED13L
    nsv5542466insertion1nstd206human GRCh38 chr12: 116,159,870-116,159,873 , GRCh37.p13 chr12: 116,597,675-116,597,678 MED13L
    nsv5512960copy number variation1nstd206human GRCh38 chr12: 116,271,306-116,272,300 , GRCh37.p13 chr12: 116,709,111-116,710,105 MED13L
    nsv5509254copy number variation1nstd206human GRCh38 chr12: 116,176,122-116,181,013 , GRCh37.p13 chr12: 116,613,927-116,618,818 MED13L
    nsv5503266copy number variation1nstd206human GRCh38 chr12: 115,992,402-115,992,560 , GRCh37.p13 chr12: 116,430,207-116,430,365 MED13L
    nsv5501396copy number variation1nstd206human GRCh38 chr12: 116,251,435-116,254,782 , GRCh37.p13 chr12: 116,689,240-116,692,587 MED13L
    nsv5500351copy number variation1nstd206human GRCh38 chr12: 116,104,237-116,110,327 , GRCh37.p13 chr12: 116,542,042-116,548,132 MED13L
    nsv5499808copy number variation1nstd206human GRCh38 chr12: 116,181,097-116,181,689 , GRCh37.p13 chr12: 116,618,902-116,619,494 MED13L
    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