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 756

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7096952copy number variation3nstd102humanUncertain significance GRCh37 chr3: 188,118,572-192,126,012 , GRCh38.p12 chr3: 188,400,784-192,408,223 P3H2, GMNC, 39 more genes
    nsv7056537inversion1nstd229human GRCh38 chr3: 188,999,506-189,014,779 , GRCh37.p13 chr3: 188,717,295-188,732,568 LOC107986167, TPRG1
    nsv7055740inversion1nstd229human GRCh38 chr3: 189,101,025-189,104,296 , GRCh37.p13 chr3: 188,818,814-188,822,085 TPRG1
    nsv7055267inversion1nstd229human GRCh38 chr3: 189,164,273-189,176,728 , GRCh37.p13 chr3: 188,882,062-188,894,517 TPRG1
    nsv7053557inversion1nstd229human GRCh38 chr3: 189,153,210-189,154,537 , GRCh37.p13 chr3: 188,870,999-188,872,326 TPRG1
    nsv7040429inversion1nstd229human GRCh38 chr3: 184,379,670-192,292,047 , GRCh37.p13 chr3: 184,097,458-192,009,836 LOC107986163, RPL34P10, 123 more genes
    nsv7039872inversion1nstd229human GRCh38 chr3: 188,997,555-188,999,967 , GRCh37.p13 chr3: 188,715,344-188,717,756 LOC107986167, TPRG1
    nsv6737696copy number variation1nstd229human GRCh38 chr3: 189,141,117-189,145,133 , GRCh37.p13 chr3: 188,858,906-188,862,922 TPRG1
    nsv6736890copy number variation1nstd229human GRCh38 chr3: 189,315,179-189,316,904 , GRCh37.p13 chr3: 189,032,968-189,034,693 TPRG1
    nsv6735932copy number variation1nstd229human GRCh38 chr3: 189,317,346-189,332,117 , GRCh37.p13 chr3: 189,035,135-189,049,906 TPRG1
    nsv6735876copy number variation1nstd229human GRCh38 chr3: 189,112,301-189,114,000 , GRCh37.p13 chr3: 188,830,090-188,831,789 TPRG1
    nsv6734740copy number variation1nstd229human GRCh38 chr3: 189,247,219-189,248,872 , GRCh37.p13 chr3: 188,965,008-188,966,661 TPRG1
    nsv6733938copy number variation1nstd229human GRCh38 chr3: 189,150,504-189,163,095 , GRCh37.p13 chr3: 188,868,293-188,880,884 TPRG1
    nsv6733894copy number variation1nstd229human GRCh38 chr3: 189,163,047-189,170,848 , GRCh37.p13 chr3: 188,880,836-188,888,637 TPRG1
    nsv6730416copy number variation1nstd229human GRCh38 chr3: 189,318,790-189,319,171 , GRCh37.p13 chr3: 189,036,579-189,036,960 TPRG1
    nsv6729764copy number variation1nstd229human GRCh38 chr3: 189,110,205-189,117,094 , GRCh37.p13 chr3: 188,827,994-188,834,883 TPRG1
    nsv6728724copy number variation1nstd229human GRCh38 chr3: 189,126,146-189,131,753 , GRCh37.p13 chr3: 188,843,935-188,849,542 TPRG1
    nsv6728293copy number variation1nstd229human GRCh38 chr3: 189,004,600-189,008,497 , GRCh37.p13 chr3: 188,722,389-188,726,286 TPRG1, LOC107986167
    nsv6728023copy number variation1nstd229human GRCh38 chr3: 189,061,605-189,061,887 , GRCh37.p13 chr3: 188,779,394-188,779,676 LOC107986167, TPRG1
    nsv6727539copy number variation1nstd229human GRCh38 chr3: 189,172,438-189,174,466 , GRCh37.p13 chr3: 188,890,227-188,892,255 TPRG1
    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