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 201

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5672604copy number variation1nstd102humanPathogenic GRCh37 chr10: 120,001-6,920,000 , GRCh38.p12 chr10: 74,061-6,878,038 PITRM1-AS1, TRV-TAC3-1, 133 more genes
    nsv5634755insertion1nstd207human GRCh38 chr10: 5,916,704-5,916,704 , GRCh37.p13 chr10: 5,958,667-5,958,667 FBH1
    nsv5311048copy number variation1nstd204human GRCh38.p13 chr10: 5,904,294-5,986,284 , GRCh37.p13 chr10: 5,946,257-6,028,247 FBH1, LOC107984200, 2 more genes
    nsv5258776copy number variation1nstd204human GRCh38.p13 chr10: 5,909,932-5,920,431 , GRCh37.p13 chr10: 5,951,895-5,962,394 FBH1
    nsv5258699copy number variation1nstd204human GRCh38.p13 chr10: 5,921,732-5,937,985 , GRCh37.p13 chr10: 5,963,695-5,979,948 FBH1, LOC105376384
    nsv5253087copy number variation1nstd204human GRCh38.p13 chr10: 5,904,301-5,986,300 , GRCh37.p13 chr10: 5,946,264-6,028,263 LOC107984200, IL15RA, 2 more genes
    nsv4969425copy number variation1nstd200human GRCh38 chr10: 5,921,665-5,921,729 , GRCh37.p13 chr10: 5,963,628-5,963,692 FBH1
    nsv4969424copy number variation1nstd200human GRCh38 chr10: 5,905,147-5,907,530 , GRCh37.p13 chr10: 5,947,110-5,949,493 FBH1
    nsv4969423copy number variation1nstd200human GRCh38 chr10: 5,898,588-5,901,677 , GRCh37.p13 chr10: 5,940,551-5,943,640 FBH1
    nsv4843667copy number variation1nstd200human GRCh37 chr10: 5,940,551-5,943,640 , GRCh38.p12 chr10: 5,898,588-5,901,677 FBH1
    nsv4829667copy number variation1nstd200human GRCh37 chr10: 5,963,628-5,963,692 , GRCh38.p12 chr10: 5,921,665-5,921,729 FBH1
    nsv4758794insertion1nstd199human GRCh37 chr10: 5,958,651-5,958,651 , GRCh38.p12 chr10: 5,916,688-5,916,688 FBH1
    nsv4615429copy number variation1nstd183human GRCh37 chr10: 5,965,229-5,977,543 , GRCh38.p12 chr10: 5,923,266-5,935,580 LOC105376384, FBH1
    nsv4565285mobile element insertion1nstd166human GRCh37.p13 chr10: 5,953,375-5,953,375 , GRCh38.p12 chr10: 5,911,412-5,911,412 FBH1
    nsv4480090mobile element insertion1nstd166human GRCh37.p13 chr10: 5,964,188-5,964,188 , GRCh38.p12 chr10: 5,922,225-5,922,225 FBH1
    nsv4456914copy number variation1nstd102humanUncertain significance GRCh37 chr10: 5,544,108-5,956,516 , GRCh38.p12 chr10: 5,502,145-5,914,553 RPL12P28, CALML3-AS1, 15 more genes
    nsv4455607copy number variation2nstd102humanPathogenic GRCh37 chr10: 100,026-15,273,144 , GRCh38.p12 chr10: 54,086-15,231,145 LOC105376357, LINC02649, 264 more genes
    nsv4189319copy number variation1nstd166human GRCh37.p13 chr10: 5,972,952-5,976,935 , GRCh38.p12 chr10: 5,930,989-5,934,972 LOC105376384, FBH1
    nsv3968780copy number variation1nstd168human GRCh38 chr10: 5,918,678-6,151,275 , GRCh37.p13 chr10: 5,960,641-6,193,238 MIR3155B, LOC107984200, 11 more genes
    nsv3936395insertion1nstd167human GRCh37 chr10: 5,958,667-5,958,667 , GRCh38.p12 chr10: 5,916,704-5,916,704 FBH1
    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