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 495

    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
    nsv6897811copy number variation1nstd229human GRCh38 chr10: 66,898,075-66,912,648 , GRCh37.p13 chr10: 68,657,833-68,672,406 LOC101928961, CTNNA3
    nsv6897619copy number variation1nstd229human GRCh38 chr10: 66,983,567-66,988,466 , GRCh37.p13 chr10: 68,743,325-68,748,224 LRRTM3, LOC101928961, 1 more genes
    nsv6897341copy number variation1nstd229human GRCh38 chr10: 66,891,258-66,904,198 , GRCh37.p13 chr10: 68,651,016-68,663,956 LOC101928961, CTNNA3
    nsv6896806copy number variation1nstd229human GRCh38 chr10: 66,645,863-67,167,778 , GRCh37.p13 chr10: 68,405,621-68,927,536 CTNNA3, LRRTM3, 1 more genes
    nsv6894831copy number variation1nstd229human GRCh38 chr10: 66,786,002-66,996,920 , GRCh37.p13 chr10: 68,545,760-68,756,678 CTNNA3, LRRTM3, 1 more genes
    nsv6894289copy number variation1nstd229human GRCh38 chr10: 66,770,095-66,946,661 , GRCh37.p13 chr10: 68,529,853-68,706,419 CTNNA3, LRRTM3, 1 more genes
    nsv6893798copy number variation1nstd229human GRCh38 chr10: 66,624,731-66,970,486 , GRCh37.p13 chr10: 68,384,489-68,730,244 CTNNA3, LRRTM3, 1 more genes
    nsv6893631copy number variation1nstd229human GRCh38 chr10: 66,977,032-67,006,335 , GRCh37.p13 chr10: 68,736,790-68,766,093 LOC101928961, CTNNA3, 1 more genes
    nsv6893584copy number variation1nstd229human GRCh38 chr10: 66,899,701-66,905,500 , GRCh37.p13 chr10: 68,659,459-68,665,258 CTNNA3, LOC101928961
    nsv6891618copy number variation1nstd229human GRCh38 chr10: 65,875,534-67,248,522 , GRCh37.p13 chr10: 67,635,292-69,008,280 CTNNA3, LRRTM3, 3 more genes
    nsv6891336copy number variation1nstd229human GRCh38 chr10: 66,964,901-66,972,900 , GRCh37.p13 chr10: 68,724,659-68,732,658 LRRTM3, LOC101928961, 1 more genes
    nsv6890046copy number variation1nstd229human GRCh38 chr10: 66,903,901-66,909,581 , GRCh37.p13 chr10: 68,663,659-68,669,339 CTNNA3, LOC101928961
    nsv6889982copy number variation1nstd229human GRCh38 chr10: 66,940,748-66,979,332 , GRCh37.p13 chr10: 68,700,506-68,739,090 LRRTM3, CTNNA3, 1 more genes
    nsv6889879copy number variation1nstd229human GRCh38 chr10: 66,957,764-67,028,495 , GRCh37.p13 chr10: 68,717,522-68,788,253 LOC101928961, CTNNA3, 1 more genes
    nsv6888139copy number variation1nstd229human GRCh38 chr10: 66,628,808-66,920,077 , GRCh37.p13 chr10: 68,388,566-68,679,835 CTNNA3, LOC101928961
    nsv6887970copy number variation1nstd229human GRCh38 chr10: 66,961,792-66,973,395 , GRCh37.p13 chr10: 68,721,550-68,733,153 LOC101928961, LRRTM3, 1 more genes
    nsv6887153copy number variation1nstd229human GRCh38 chr10: 66,986,240-66,989,401 , GRCh37.p13 chr10: 68,745,998-68,749,159 LOC101928961, LRRTM3, 1 more genes
    nsv6887138copy number variation1nstd229human GRCh38 chr10: 66,966,101-66,972,900 , GRCh37.p13 chr10: 68,725,859-68,732,658 LRRTM3, CTNNA3, 1 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