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 789

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7043432inversion1nstd229human GRCh38 chr4: 117,041,189-125,064,058 , GRCh37.p13 chr4: 117,962,345-125,985,213 SEPTIN14P4, LINC02516, 109 more genes
    nsv7039429inversion1nstd229human GRCh38 chr4: 118,892,252-118,892,352 , GRCh37.p13 chr4: 119,813,407-119,813,507 SYNPO2
    nsv6757554copy number variation1nstd229human GRCh38 chr4: 119,007,765-119,011,856 , GRCh37.p13 chr4: 119,928,920-119,933,011 SYNPO2
    nsv6757115copy number variation1nstd229human GRCh38 chr4: 118,981,567-118,989,388 , GRCh37.p13 chr4: 119,902,722-119,910,543 SYNPO2, LOC105377394
    nsv6755294copy number variation1nstd229human GRCh38 chr4: 119,010,051-119,020,017 , GRCh37.p13 chr4: 119,931,206-119,941,172 SYNPO2
    nsv6752771copy number variation1nstd229human GRCh38 chr4: 118,989,401-118,989,739 , GRCh37.p13 chr4: 119,910,556-119,910,894 SYNPO2
    nsv6752324copy number variation1nstd229human GRCh38 chr4: 118,976,164-118,976,295 , GRCh37.p13 chr4: 119,897,319-119,897,450 SYNPO2, LOC105377394
    nsv6751464copy number variation1nstd229human GRCh38 chr4: 118,843,701-118,864,100 , GRCh37.p13 chr4: 119,764,856-119,785,255 SYNPO2
    nsv6750467copy number variation1nstd229human GRCh38 chr4: 119,011,319-119,011,964 , GRCh37.p13 chr4: 119,932,474-119,933,119 SYNPO2
    nsv6750231copy number variation1nstd229human GRCh38 chr4: 118,887,801-118,896,200 , GRCh37.p13 chr4: 119,808,956-119,817,355 SYNPO2
    nsv6749913copy number variation1nstd229human GRCh38 chr4: 118,700,501-118,891,200 , GRCh37.p13 chr4: 119,621,656-119,812,355 LOC105377393, METTL14, 2 more genes
    nsv6749865copy number variation1nstd229human GRCh38 chr4: 118,969,586-118,974,207 , GRCh37.p13 chr4: 119,890,741-119,895,362 SYNPO2, LOC105377394
    nsv6747754copy number variation1nstd229human GRCh38 chr4: 118,864,098-118,864,126 , GRCh37.p13 chr4: 119,785,253-119,785,281 SYNPO2
    nsv6747641copy number variation1nstd229human GRCh38 chr4: 118,975,391-118,979,187 , GRCh37.p13 chr4: 119,896,546-119,900,342 LOC105377394, SYNPO2
    nsv6747179copy number variation1nstd229human GRCh38 chr4: 118,960,498-118,964,256 , GRCh37.p13 chr4: 119,881,653-119,885,411 LOC105377394, SYNPO2
    nsv6746830copy number variation1nstd229human GRCh38 chr4: 119,020,927-119,067,921 , GRCh37.p13 chr4: 119,942,082-119,989,076 SYNPO2
    nsv6746524copy number variation1nstd229human GRCh38 chr4: 118,970,555-118,970,935 , GRCh37.p13 chr4: 119,891,710-119,892,090 SYNPO2, LOC105377394
    nsv6746369copy number variation1nstd229human GRCh38 chr4: 118,911,077-118,925,524 , GRCh37.p13 chr4: 119,832,232-119,846,679 SYNPO2
    nsv6745280copy number variation1nstd229human GRCh38 chr4: 119,022,983-119,023,019 , GRCh37.p13 chr4: 119,944,138-119,944,174 SYNPO2
    nsv6745093copy number variation1nstd229human GRCh38 chr4: 119,048,401-119,070,500 , GRCh37.p13 chr4: 119,969,556-119,991,655 SYNPO2
    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