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 944

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7141147insertion1nstd232human GRCh37.p13 chr3: 57,003,274-57,003,274 , GRCh38.p12 chr3: 56,969,246-56,969,246 ARHGEF3
    nsv7137843insertion1nstd232human GRCh37.p13 chr3: 57,003,273-57,003,273 , GRCh38.p12 chr3: 56,969,245-56,969,245 ARHGEF3
    nsv7051968inversion1nstd229human GRCh38 chr3: 56,944,702-65,952,705 , GRCh37.p13 chr3: 56,978,730-65,938,380 ILF2P1, ARHGEF3-AS1, 115 more genes
    nsv7042298inversion1nstd229human GRCh38 chr3: 56,614,465-56,741,689 , GRCh37.p13 chr3: 56,648,493-56,775,717 CCDC66, ARHGEF3, 1 more genes
    nsv7038236inversion1nstd229human GRCh38 chr3: 56,950,550-57,362,669 , GRCh37.p13 chr3: 56,984,578-57,369,477 SPATA12, APPL1, 9 more genes
    nsv6715622copy number variation1nstd229human GRCh38 chr3: 56,977,890-56,980,235 , GRCh37.p13 chr3: 57,011,918-57,014,263 ARHGEF3
    nsv6714570copy number variation1nstd229human GRCh38 chr3: 56,782,554-56,792,260 , GRCh37.p13 chr3: 56,816,582-56,826,288 ARHGEF3
    nsv6713495copy number variation1nstd229human GRCh38 chr3: 56,980,101-56,985,000 , GRCh37.p13 chr3: 57,014,129-57,019,028 ARHGEF3
    nsv6711958copy number variation1nstd229human GRCh38 chr3: 56,974,516-56,974,688 , GRCh37.p13 chr3: 57,008,544-57,008,716 ARHGEF3
    nsv6711553copy number variation1nstd229human GRCh38 chr3: 56,820,001-57,251,300 , GRCh37.p13 chr3: 56,854,029-57,285,328 HESX1, ARHGEF3-AS1, 6 more genes
    nsv6711241copy number variation1nstd229human GRCh38 chr3: 56,760,669-56,766,816 , GRCh37.p13 chr3: 56,794,697-56,800,844 ARHGEF3
    nsv6710491copy number variation1nstd229human GRCh38 chr3: 56,842,932-56,856,870 , GRCh37.p13 chr3: 56,876,960-56,890,898 ARHGEF3
    nsv6710206copy number variation1nstd229human GRCh38 chr3: 56,921,603-56,924,466 , GRCh37.p13 chr3: 56,955,631-56,958,494 ARHGEF3
    nsv6709204copy number variation1nstd229human GRCh38 chr3: 56,794,836-56,801,733 , GRCh37.p13 chr3: 56,828,864-56,835,761 ARHGEF3
    nsv6708946copy number variation1nstd229human GRCh38 chr3: 57,037,623-57,045,016 , GRCh37.p13 chr3: 57,071,651-57,079,044 ARHGEF3
    nsv6708820copy number variation1nstd229human GRCh38 chr3: 56,887,617-56,905,468 , GRCh37.p13 chr3: 56,921,645-56,939,496 ARHGEF3
    nsv6708322copy number variation1nstd229human GRCh38 chr3: 56,793,001-56,812,300 , GRCh37.p13 chr3: 56,827,029-56,846,328 ARHGEF3
    nsv6708302copy number variation1nstd229human GRCh38 chr3: 56,959,011-56,962,138 , GRCh37.p13 chr3: 56,993,039-56,996,166 ARHGEF3-AS1, ARHGEF3
    nsv6706824copy number variation1nstd229human GRCh38 chr3: 56,969,246-56,969,405 , GRCh37.p13 chr3: 57,003,274-57,003,433 ARHGEF3
    nsv6706717copy number variation1nstd229human GRCh38 chr3: 57,023,225-57,025,521 , GRCh37.p13 chr3: 57,057,253-57,059,549 ARHGEF3
    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