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 487

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5979630insertion1nstd209human GRCh38 chr11: 8,424,809-8,424,809 , GRCh37.p13 chr11: 8,446,356-8,446,356 STK33
    nsv5979277insertion1nstd209human GRCh38 chr11: 8,557,276-8,557,276 , GRCh37.p13 chr11: 8,578,823-8,578,823 STK33
    nsv5923733copy number variation1nstd209human GRCh38 chr11: 8,422,993-8,425,057 , GRCh37.p13 chr11: 8,444,540-8,446,604 STK33
    nsv5923342copy number variation1nstd209human GRCh38 chr11: 8,448,857-8,449,693 , GRCh37.p13 chr11: 8,470,404-8,471,240 STK33
    nsv5917908copy number variation1nstd209human GRCh38 chr11: 8,458,558-8,458,706 , GRCh37.p13 chr11: 8,480,105-8,480,253 STK33
    nsv5864803copy number variation1nstd209human GRCh38 chr11: 8,500,274-8,501,473 , GRCh37.p13 chr11: 8,521,821-8,523,020 STK33
    nsv5858883copy number variation1nstd209human GRCh38 chr11: 8,423,240-8,424,749 , GRCh37.p13 chr11: 8,444,787-8,446,296 STK33
    nsv5729420mobile element insertion1nstd211human GRCh38 chr11: 8,437,677-8,437,677 , GRCh37.p13 chr11: 8,459,224-8,459,224 STK33
    nsv5722040mobile element insertion2nstd211human GRCh38 chr11: 8,423,000-8,423,000 , GRCh37.p13 chr11: 8,444,547-8,444,547 STK33
    nsv5718934mobile element insertion1nstd211human GRCh38 chr11: 8,546,089-8,546,089 , GRCh37.p13 chr11: 8,567,636-8,567,636 STK33
    nsv5713522mobile element insertion2nstd211human GRCh38 chr11: 8,573,092-8,573,092 , GRCh37.p13 chr11: 8,594,639-8,594,639 STK33
    nsv5695356mobile element insertion2nstd211human GRCh38 chr11: 8,424,826-8,424,826 , GRCh37.p13 chr11: 8,446,373-8,446,373 STK33
    nsv5662904insertion1nstd207human GRCh38 chr11: 8,424,809-8,424,809 , GRCh37.p13 chr11: 8,446,356-8,446,356 STK33
    nsv5662768insertion1nstd207human GRCh38 chr11: 8,571,890-8,571,890 , GRCh37.p13 chr11: 8,593,437-8,593,437 STK33
    nsv5662567insertion1nstd207human GRCh38 chr11: 8,371,735-8,371,735 , GRCh37.p13 chr11: 8,393,282-8,393,282 STK33
    nsv5657740insertion1nstd207human GRCh38 chr11: 8,557,286-8,557,286 , GRCh37.p13 chr11: 8,578,833-8,578,833 STK33
    nsv5654001insertion1nstd207human GRCh38 chr11: 8,553,750-8,553,750 , GRCh37.p13 chr11: 8,575,297-8,575,297 STK33
    nsv5645915insertion1nstd207human GRCh38 chr11: 8,571,897-8,571,897 , GRCh37.p13 chr11: 8,593,444-8,593,444 STK33
    nsv5598622copy number variation1nstd207human GRCh38 chr11: 8,448,857-8,449,693 , GRCh37.p13 chr11: 8,470,404-8,471,240 STK33
    nsv5561648inversion1nstd206human GRCh38 chr11: 8,445,727-8,493,762 , GRCh37.p13 chr11: 8,467,274-8,515,309 STK33
    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