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 181

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5943623copy number variation1nstd209human GRCh38 chr15: 40,725,866-40,726,792 , GRCh37.p13 chr15: 41,018,064-41,018,990 RAD51
    nsv5934517copy number variation1nstd209human GRCh38 chr15: 40,707,243-40,707,552 , GRCh37.p13 chr15: 40,999,441-40,999,750 RAD51
    nsv5702979mobile element insertion1nstd211human GRCh38 chr15: 40,714,012-40,714,012 , GRCh37.p13 chr15: 41,006,210-41,006,210 RAD51
    nsv5507012copy number variation1nstd206human GRCh38 chr15: 40,725,899-40,726,786 , GRCh37.p13 chr15: 41,018,097-41,018,984 RAD51
    nsv5506349copy number variation1nstd206human GRCh38 chr15: 40,719,335-40,727,575 , GRCh37.p13 chr15: 41,011,533-41,019,773 RAD51
    nsv5380758copy number variation2nstd102humanUncertain significance GRCh37 chr15: 32,964,879-91,358,519 , GRCh38.p12 chr15: 32,672,678-90,815,289 LOC105370794, HNRNPA1P45, 1173 more genes
    nsv5038422inversion1nstd200human GRCh38 chr15: 40,121,948-64,050,807 , GRCh37.p13 chr15: 40,414,149-64,343,006 , EIF4EBP2P2, 475 more genes
    nsv5001382copy number variation1nstd200human GRCh38 chr15: 40,713,903-40,716,612 , GRCh37.p13 chr15: 41,006,101-41,008,810 RAD51
    nsv5001381copy number variation1nstd200human GRCh38 chr15: 40,710,790-40,713,963 , GRCh37.p13 chr15: 41,002,988-41,006,161 RAD51
    nsv4872280inversion1nstd200human GRCh37 chr15: 40,414,149-64,343,008 , GRCh38.p12 chr15: 40,121,948-64,050,809 , DNAAF4-CCPG1, 475 more genes
    nsv4855953copy number variation1nstd200human GRCh37 chr15: 41,018,076-41,018,961 , GRCh38.p12 chr15: 40,725,878-40,726,763 RAD51
    nsv4855952copy number variation1nstd200human GRCh37 chr15: 41,006,101-41,008,810 , GRCh38.p12 chr15: 40,713,903-40,716,612 RAD51
    nsv4855951copy number variation1nstd200human GRCh37 chr15: 41,002,989-41,006,161 , GRCh38.p12 chr15: 40,710,791-40,713,963 RAD51
    nsv4855949copy number variation1nstd200human GRCh37 chr15: 40,970,855-40,985,713 , GRCh38.p12 chr15: 40,678,657-40,693,515 RAD51, RAD51-AS1
    nsv4729095copy number variation1nstd102humanUncertain significance GRCh37 chr15: 40,464,942-41,196,807 , GRCh38.p12 chr15: 40,172,741-40,904,609 SPINT1-AS1, KNSTRN, 37 more genes
    nsv4619588copy number variation1nstd183human GRCh37 chr15: 40,978,726-40,991,153 , GRCh38.p12 chr15: 40,686,528-40,698,955 RAD51, RAD51-AS1
    nsv4576625mobile element insertion1nstd166human GRCh37.p13 chr15: 41,001,520-41,001,520 , GRCh38.p12 chr15: 40,709,322-40,709,322 RAD51
    nsv4457236copy number variation1nstd102humanUncertain significance GRCh37 chr15: 40,944,610-41,001,292 , GRCh38.p12 chr15: 40,652,412-40,709,094 RAD51, RAD51-AS1, 1 more genes
    nsv4436396complex substitution1nstd102humanPathogenic GRCh38.p12 chr15: 34,346,036-41,764,885 , GRCh37 chr15: 34,638,237-42,057,083 ACTC1, BUB1B, 150 more genes
    nsv4248630copy number variation1nstd166human GRCh37.p13 chr15: 41,018,097-41,018,984 , GRCh38.p12 chr15: 40,725,899-40,726,786 RAD51
    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