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 431

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5972566inversion1nstd209human GRCh38 chr11: 11,873,592-11,890,293 , GRCh37.p13 chr11: 11,895,139-11,911,840 USP47
    nsv5972035insertion1nstd209human GRCh38 chr11: 11,926,961-11,926,961 , GRCh37.p13 chr11: 11,948,508-11,948,508 USP47
    nsv5923327copy number variation1nstd209human GRCh38 chr11: 11,873,681-11,877,272 , GRCh37.p13 chr11: 11,895,228-11,898,819 USP47
    nsv5920149copy number variation1nstd209human GRCh38 chr11: 11,854,051-11,855,010 , GRCh37.p13 chr11: 11,875,598-11,876,557 H3P33, USP47
    nsv5915209copy number variation1nstd209human GRCh38 chr11: 11,863,044-11,870,501 , GRCh37.p13 chr11: 11,884,591-11,892,048 USP47
    nsv5913008copy number variation1nstd209human GRCh38 chr11: 11,916,933-11,917,018 , GRCh37.p13 chr11: 11,938,480-11,938,565 USP47
    nsv5859795copy number variation1nstd209human GRCh38 chr11: 11,863,010-11,870,516 , GRCh37.p13 chr11: 11,884,557-11,892,063 USP47
    nsv5730934mobile element insertion2nstd211human GRCh38 chr11: 11,926,978-11,926,978 , GRCh37.p13 chr11: 11,948,525-11,948,525 USP47
    nsv5707060mobile element insertion2nstd211human GRCh38 chr11: 11,945,651-11,945,651 , GRCh37.p13 chr11: 11,967,198-11,967,198 USP47
    nsv5701087mobile element insertion1nstd211human GRCh38 chr11: 11,847,601-11,847,601 , GRCh37.p13 chr11: 11,869,148-11,869,148 USP47
    nsv5650645insertion1nstd207human GRCh38 chr11: 11,926,961-11,926,961 , GRCh37.p13 chr11: 11,948,508-11,948,508 USP47
    nsv5598004copy number variation1nstd207human GRCh38 chr11: 11,854,051-11,855,010 , GRCh37.p13 chr11: 11,875,598-11,876,557 USP47, H3P33
    nsv5589971copy number variation1nstd207human GRCh38 chr11: 11,916,933-11,917,018 , GRCh37.p13 chr11: 11,938,480-11,938,565 USP47
    nsv5555058mobile element insertion1nstd206human GRCh38 chr11: 11,926,978-11,927,029 , GRCh37.p13 chr11: 11,948,525-11,948,576 USP47
    nsv5541012insertion1nstd206human GRCh38 chr11: 11,945,651-11,945,653 , GRCh37.p13 chr11: 11,967,198-11,967,200 USP47
    nsv5511677copy number variation1nstd206human GRCh38 chr11: 11,898,488-11,899,170 , GRCh37.p13 chr11: 11,920,035-11,920,717 USP47
    nsv5511676copy number variation1nstd206human GRCh38 chr11: 11,854,065-11,855,052 , GRCh37.p13 chr11: 11,875,612-11,876,599 H3P33, USP47
    nsv5511565copy number variation1nstd206human GRCh38 chr11: 11,924,977-11,925,078 , GRCh37.p13 chr11: 11,946,524-11,946,625 USP47
    nsv5500115copy number variation1nstd206human GRCh38 chr11: 11,916,936-11,917,019 , GRCh37.p13 chr11: 11,938,483-11,938,566 USP47
    nsv5496483copy number variation1nstd206human GRCh38 chr11: 11,944,547-11,969,111 , GRCh37.p13 chr11: 11,966,094-11,990,658 USP47, DKK3
    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