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 188

    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
    nsv7073417inversion1nstd229human GRCh38 chr10: 121,974,813-121,974,922 , GRCh37.p13 chr10: 123,734,328-123,734,437 NSMCE4A
    nsv7068192inversion1nstd229human GRCh38 chr10: 118,910,158-125,783,778 , GRCh37.p13 chr10: 120,669,670-127,472,347 CTBP2, RPS26P39, 114 more genes
    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
    nsv6890338copy number variation1nstd229human GRCh38 chr10: 121,964,434-121,964,729 , GRCh37.p13 chr10: 123,723,949-123,724,244 NSMCE4A
    nsv6884703copy number variation1nstd229human GRCh38 chr10: 121,934,615-128,427,106 , GRCh37.p13 chr10: 123,694,130-130,225,370 OAT, C10orf88, 98 more genes
    nsv6879734copy number variation1nstd229human GRCh38 chr10: 121,971,631-121,972,459 , GRCh37.p13 chr10: 123,731,146-123,731,974 NSMCE4A
    nsv6878095copy number variation1nstd229human GRCh38 chr10: 121,966,601-121,969,400 , GRCh37.p13 chr10: 123,726,116-123,728,915 NSMCE4A
    nsv6620171copy number variation1nstd224human GRCh37 chr10: 123,609,009-123,779,171 , GRCh38.p12 chr10: 121,849,494-122,019,656 ATE1, ATE1-AS1, 2 more genes
    nsv6620081copy number variation1nstd224human GRCh37 chr10: 123,557,361-123,782,114 , GRCh38.p12 chr10: 121,797,846-122,022,599 ATE1, NSMCE4A, 2 more genes
    nsv6585886inversion1nstd223human GRCh38 chr10: 118,910,158-125,783,778 , GRCh37.p13 chr10: 120,669,670-127,472,347 LOC105378520, SPADH, 114 more genes
    nsv6442656copy number variation1nstd223human GRCh38 chr10: 121,974,001-121,975,600 , GRCh37.p13 chr10: 123,733,516-123,735,115 NSMCE4A
    nsv6437047copy number variation1nstd223human GRCh38 chr10: 121,934,743-121,980,419 , GRCh37.p13 chr10: 123,694,258-123,739,934 ATE1-AS1, NSMCE4A
    nsv6436213copy number variation1nstd223human GRCh38 chr10: 121,972,123-121,973,203 , GRCh37.p13 chr10: 123,731,638-123,732,718 NSMCE4A
    nsv6314129copy number variation1nstd102humanPathogenic GRCh37 chr10: 117,019,650-125,217,066 , GRCh38.p12 chr10: 115,260,173-123,457,550 PDZD8, MIR3663HG, 122 more genes
    nsv6314085copy number variation1nstd102humanPathogenic GRCh37 chr10: 108,455,687-135,427,143 , GRCh38.p12 chr10: 106,695,929-133,613,639 LOC107984268, DPYSL4, 379 more genes
    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