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 241

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6113170mobile element insertion1nstd186human GRCh37 chr13: 44,411,785-44,411,813 , GRCh38.p12 chr13: 43,837,649-43,837,677 CCDC122
    nsv5971687insertion1nstd209human GRCh38 chr13: 43,879,814-43,879,814 , GRCh37.p13 chr13: 44,453,950-44,453,950 LACC1, CCDC122
    nsv5710742mobile element insertion1nstd211human GRCh38 chr13: 43,837,649-43,837,649 , GRCh37.p13 chr13: 44,411,785-44,411,785 CCDC122
    nsv5706800mobile element insertion1nstd211human GRCh38 chr13: 43,837,177-43,837,177 , GRCh37.p13 chr13: 44,411,313-44,411,313 CCDC122
    nsv5661729insertion1nstd207human GRCh38 chr13: 43,837,637-43,837,637 , GRCh37.p13 chr13: 44,411,773-44,411,773 CCDC122
    nsv5648286insertion1nstd207human GRCh38 chr13: 43,879,800-43,879,800 , GRCh37.p13 chr13: 44,453,936-44,453,936 LACC1, CCDC122
    nsv5644670insertion1nstd207human GRCh38 chr13: 43,869,953-43,869,953 , GRCh37.p13 chr13: 44,444,089-44,444,089 CCDC122
    nsv5564510copy number variation1nstd102humanPathogenic GRCh37 chr13: 19,053,605-115,108,528 , GRCh38.p12 chr13: 18,479,465-114,343,053 RN7SL272P, DIAPH3, 1333 more genes
    nsv5507565copy number variation1nstd206human GRCh38 chr13: 43,849,903-43,851,175 , GRCh37.p13 chr13: 44,424,039-44,425,311 CCDC122
    nsv5501096copy number variation1nstd206human GRCh38 chr13: 43,818,000-43,842,106 , GRCh37.p13 chr13: 44,392,136-44,416,242 CCDC122
    nsv5421191mobile element insertion1nstd206human GRCh38 chr13: 43,837,649-43,837,677 , GRCh37.p13 chr13: 44,411,785-44,411,813 CCDC122
    nsv5416194mobile element insertion1nstd206human GRCh38 chr13: 43,837,177-43,837,228 , GRCh37.p13 chr13: 44,411,313-44,411,364 CCDC122
    nsv5272167copy number variation1nstd204human GRCh38.p13 chr13: 43,842,401-43,845,200 , GRCh37.p13 chr13: 44,416,537-44,419,336 CCDC122
    nsv5188477mobile element insertion1nstd203human GRCh38 chr13: 43,868,377-43,868,388 , GRCh37.p13 chr13: 44,442,513-44,442,524 CCDC122
    nsv5181412mobile element insertion1nstd203human GRCh38 chr13: 43,832,097-43,832,107 , GRCh37.p13 chr13: 44,406,233-44,406,243 CCDC122
    nsv5155051mobile element insertion1nstd203human GRCh38 chr13: 43,837,168-43,837,177 , GRCh37.p13 chr13: 44,411,304-44,411,313 CCDC122
    nsv5154574mobile element insertion1nstd203human GRCh38 chr13: 43,837,164-43,837,177 , GRCh37.p13 chr13: 44,411,300-44,411,313 CCDC122
    nsv5150703mobile element insertion1nstd203human GRCh38 chr13: 43,837,637-43,837,649 , GRCh37.p13 chr13: 44,411,773-44,411,785 CCDC122
    nsv5146292mobile element insertion1nstd203human GRCh38 chr13: 43,837,636-43,837,649 , GRCh37.p13 chr13: 44,411,772-44,411,785 CCDC122
    nsv5143204mobile element insertion1nstd203human GRCh38 chr13: 43,837,641-43,837,649 , GRCh37.p13 chr13: 44,411,777-44,411,785 CCDC122
    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