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 890

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137211copy number variation1nstd102humanPathogenic GRCh37 chr10: 11,138,692-135,427,143 , GRCh38.p12 chr10: 11,096,729-133,613,639 EXOC6, VCL, 1906 more genes
    nsv7137209copy number variation1nstd102humanPathogenic GRCh37 chr10: 12,829,206-135,427,143 , GRCh38.p12 chr10: 12,787,207-133,613,639 RNU7-12P, RNU1-65P, 1876 more genes
    nsv7137208copy number variation1nstd102humanPathogenic GRCh37 chr10: 123,477,898-135,427,143 , GRCh38.p12 chr10: 121,718,384-133,613,639 ZRANB1, LOC105378544, 182 more genes
    nsv7098893copy number variation1nstd102humanPathogenic GRCh37 chr10: 122,610,933-135,439,810 , GRCh38.p12 chr10: 120,851,421-133,626,306 LOC105378571, DOCK1, 196 more genes
    nsv7093623copy number variation1nstd102humanUncertain significance GRCh37 chr10: 123,239,371-124,813,281 , GRCh38.p12 chr10: 121,479,857-123,053,765 TACC2, BTBD16, 25 more genes
    nsv7071429inversion1nstd229human GRCh38 chr10: 122,195,827-122,195,990 , GRCh37.p13 chr10: 123,955,342-123,955,505 TACC2
    nsv7068192inversion1nstd229human GRCh38 chr10: 118,910,158-125,783,778 , GRCh37.p13 chr10: 120,669,670-127,472,347 CTBP2, RPS26P39, 114 more genes
    nsv7058647inversion1nstd229human GRCh38 chr10: 122,039,913-122,040,072 , GRCh37.p13 chr10: 123,799,428-123,799,587 TACC2
    nsv6897985copy number variation1nstd229human GRCh38 chr10: 122,175,240-122,178,491 , GRCh37.p13 chr10: 123,934,755-123,938,006 TACC2
    nsv6896913copy number variation1nstd229human GRCh38 chr10: 121,989,078-121,992,725 , GRCh37.p13 chr10: 123,748,593-123,752,240 TACC2
    nsv6896792copy number variation1nstd229human GRCh38 chr10: 122,248,901-122,287,367 , GRCh37.p13 chr10: 124,008,416-124,046,882 TACC2, BTBD16
    nsv6896474copy number variation1nstd229human GRCh38 chr10: 122,233,564-122,236,099 , GRCh37.p13 chr10: 123,993,079-123,995,614 TACC2
    nsv6895678copy number variation1nstd229human GRCh38 chr10: 122,022,583-122,022,777 , GRCh37.p13 chr10: 123,782,098-123,782,292 TACC2
    nsv6895318copy number variation1nstd229human GRCh38 chr10: 122,199,680-122,201,668 , GRCh37.p13 chr10: 123,959,195-123,961,183 TACC2
    nsv6893531copy number variation1nstd229human GRCh38 chr10: 122,049,892-122,055,140 , GRCh37.p13 chr10: 123,809,407-123,814,655 TACC2
    nsv6893394copy number variation1nstd229human GRCh38 chr10: 122,043,801-122,048,400 , GRCh37.p13 chr10: 123,803,316-123,807,915 TACC2
    nsv6892577copy number variation1nstd229human GRCh38 chr10: 121,685,649-124,297,191 , GRCh37.p13 chr10: 123,445,163-125,985,760 LOC107984128, ATE1-AS1, 39 more genes
    nsv6892383copy number variation1nstd229human GRCh38 chr10: 121,998,927-122,003,999 , GRCh37.p13 chr10: 123,758,442-123,763,514 TACC2
    nsv6892004copy number variation1nstd229human GRCh38 chr10: 122,121,865-122,129,343 , GRCh37.p13 chr10: 123,881,380-123,888,858 TACC2
    nsv6891277copy number variation1nstd229human GRCh38 chr10: 122,028,688-122,085,847 , GRCh37.p13 chr10: 123,788,203-123,845,362 TACC2
    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