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 912

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6123668insertion1nstd186human GRCh37 chr5: 169,366,221-169,366,243 , GRCh38.p12 chr5: 169,939,217-169,939,239 INSYN2B, DOCK2
    nsv6113667mobile element insertion1nstd186human GRCh37 chr5: 169,253,973-169,254,024 , GRCh38.p12 chr5: 169,826,969-169,827,020 DOCK2
    nsv5977268inversion1nstd209human GRCh38 chr5: 169,797,536-169,797,732 , GRCh37.p13 chr5: 169,224,540-169,224,736 DOCK2
    nsv5967424insertion1nstd209human GRCh38 chr5: 169,949,675-169,949,675 , GRCh37.p13 chr5: 169,376,679-169,376,679 DOCK2, INSYN2B
    nsv5966892insertion1nstd209human GRCh38 chr5: 169,993,907-169,993,907 , GRCh37.p13 chr5: 169,420,911-169,420,911 DOCK2
    nsv5953785insertion1nstd209human GRCh38 chr5: 169,939,239-169,939,239 , GRCh37.p13 chr5: 169,366,243-169,366,243 DOCK2, INSYN2B
    nsv5949032insertion1nstd209human GRCh38 chr5: 169,826,954-169,826,954 , GRCh37.p13 chr5: 169,253,958-169,253,958 DOCK2
    nsv5904980copy number variation1nstd209human GRCh38 chr5: 170,012,229-170,012,285 , GRCh37.p13 chr5: 169,439,233-169,439,289 DOCK2
    nsv5902620copy number variation1nstd209human GRCh38 chr5: 169,866,011-169,866,071 , GRCh37.p13 chr5: 169,293,015-169,293,075 DOCK2, INSYN2B
    nsv5899031copy number variation1nstd209human GRCh38 chr5: 169,776,140-169,776,206 , GRCh37.p13 chr5: 169,203,144-169,203,210 DOCK2
    nsv5898227copy number variation1nstd209human GRCh38 chr5: 169,645,040-169,650,293 , GRCh37.p13 chr5: 169,072,044-169,077,297 DOCK2
    nsv5895277copy number variation1nstd209human GRCh38 chr5: 170,040,686-170,040,944 , GRCh37.p13 chr5: 169,467,690-169,467,948 DOCK2
    nsv5892338copy number variation1nstd209human GRCh38 chr5: 169,947,790-169,947,853 , GRCh37.p13 chr5: 169,374,794-169,374,857 INSYN2B, DOCK2
    nsv5887633copy number variation1nstd209human GRCh38 chr5: 170,013,106-170,014,054 , GRCh37.p13 chr5: 169,440,110-169,441,058 DOCK2
    nsv5842173copy number variation2nstd209human GRCh38 chr5: 170,013,129-170,014,128 , GRCh37.p13 chr5: 169,440,133-169,441,132 DOCK2
    nsv5842117copy number variation1nstd209human GRCh38 chr5: 169,644,988-169,650,292 , GRCh37.p13 chr5: 169,071,992-169,077,296 DOCK2
    nsv5841569copy number variation1nstd209human GRCh38 chr5: 169,949,693-169,950,892 , GRCh37.p13 chr5: 169,376,697-169,377,896 INSYN2B, DOCK2
    nsv5841568copy number variation1nstd209human GRCh38 chr5: 169,939,601-169,940,900 , GRCh37.p13 chr5: 169,366,605-169,367,904 INSYN2B, DOCK2
    nsv5730039mobile element insertion1nstd211human GRCh38 chr5: 169,920,946-169,920,946 , GRCh37.p13 chr5: 169,347,950-169,347,950 INSYN2B, DOCK2
    nsv5729601mobile element insertion2nstd211human GRCh38 chr5: 169,949,688-169,949,688 , GRCh37.p13 chr5: 169,376,692-169,376,692 DOCK2, INSYN2B
    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