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 261

    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
    nsv7093866copy number variation1nstd102humanLikely pathogenic GRCh37 chr10: 13,152,353-13,162,081 , GRCh38.p12 chr10: 13,110,353-13,120,081 OPTN
    nsv7093783copy number variation1nstd102humanPathogenic GRCh37 chr10: 13,164,365-13,168,059 , GRCh38.p12 chr10: 13,122,365-13,126,059 OPTN
    nsv7093782copy number variation1nstd102humanPathogenic GRCh37 chr10: 13,151,123-13,158,360 , GRCh38.p12 chr10: 13,109,123-13,116,360 OPTN
    nsv7093706copy number variation1nstd102humanPathogenic GRCh37 chr10: 13,154,433-13,161,060 , GRCh38.p12 chr10: 13,112,433-13,119,060 OPTN
    nsv7093625copy number variation1nstd102humanUncertain significance GRCh37 chr10: 13,158,247-13,169,923 , GRCh38.p12 chr10: 13,116,247-13,127,923 OPTN
    nsv7073282inversion1nstd229human GRCh38 chr10: 12,099,288-14,830,781 , GRCh37.p13 chr10: 12,141,287-14,872,780 MIR1265, RNA5SP301, 45 more genes
    nsv7061969inversion1nstd229human GRCh38 chr10: 11,128,019-14,526,691 , GRCh37.p13 chr10: 11,169,982-14,568,690 RPL5P25, LOC105376425, 58 more genes
    nsv7058695inversion1nstd229human GRCh38 chr10: 11,787,108-13,297,144 , GRCh37.p13 chr10: 11,829,107-13,339,144 RNU6-6P, SEC61A2, 28 more genes
    nsv6897460copy number variation1nstd229human GRCh38 chr10: 12,756,919-13,101,343 , GRCh37.p13 chr10: 12,798,918-13,143,343 LOC105376418, OPTN, 4 more genes
    nsv6894400copy number variation1nstd229human GRCh38 chr10: 13,114,133-13,146,145 , GRCh37.p13 chr10: 13,156,133-13,188,145 OPTN
    nsv6889770copy number variation1nstd229human GRCh38 chr10: 13,117,362-13,120,211 , GRCh37.p13 chr10: 13,159,362-13,162,211 OPTN
    nsv6887870copy number variation1nstd229human GRCh38 chr10: 13,132,946-13,139,255 , GRCh37.p13 chr10: 13,174,946-13,181,255 OPTN
    nsv6885863copy number variation1nstd229human GRCh38 chr10: 13,109,690-13,122,163 , GRCh37.p13 chr10: 13,151,690-13,164,163 OPTN
    nsv6879206copy number variation1nstd229human GRCh38 chr10: 13,110,041-13,120,564 , GRCh37.p13 chr10: 13,152,041-13,162,564 OPTN
    nsv6879031copy number variation1nstd229human GRCh38 chr10: 13,127,005-13,134,874 , GRCh37.p13 chr10: 13,169,005-13,176,874 OPTN
    nsv6878281copy number variation1nstd229human GRCh38 chr10: 13,135,792-13,170,011 , GRCh37.p13 chr10: 13,177,792-13,212,011 OPTN, MCM10, 2 more genes
    nsv6637819copy number variation1nstd102humanUncertain significance GRCh37 chr10: 12,810,570-13,149,670 , GRCh38.p12 chr10: 12,768,571-13,107,670 CAMK1D, RNA5SP300, 5 more genes
    nsv6620175copy number variation1nstd224human GRCh37 chr10: 13,060,410-13,150,265 , GRCh38.p12 chr10: 13,018,410-13,108,265 OPTN, RPL5P25, 2 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