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 268

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5715039mobile element insertion1nstd211human GRCh38 chr1: 112,912,379-112,912,379 , GRCh37.p13 chr1: 113,455,001-113,455,001 SLC16A1
    nsv5694193mobile element insertion2nstd211human GRCh38 chr1: 112,951,358-112,951,358 , GRCh37.p13 chr1: 113,493,980-113,493,980 SLC16A1
    nsv5679210mobile element insertion2nstd211human GRCh38 chr1: 112,934,687-112,934,687 , GRCh37.p13 chr1: 113,477,309-113,477,309 SLC16A1
    nsv5555507mobile element insertion1nstd206human GRCh38 chr1: 112,912,379-112,912,430 , GRCh37.p13 chr1: 113,455,001-113,455,052 SLC16A1
    nsv5429360copy number variation1nstd206human GRCh38 chr1: 111,687,835-115,150,000 , GRCh37.p13 chr1: 112,230,457-115,692,621 , ST7L, 77 more genes
    nsv5424028copy number variation1nstd206human GRCh38 chr1: 112,912,860-112,913,402 , GRCh37.p13 chr1: 113,455,482-113,456,024 SLC16A1
    nsv5410373mobile element insertion1nstd206human GRCh38 chr1: 112,934,687-112,934,738 , GRCh37.p13 chr1: 113,477,309-113,477,360 SLC16A1
    nsv5402397mobile element insertion1nstd206human GRCh38 chr1: 112,951,346-112,951,346 , GRCh37.p13 chr1: 113,493,968-113,493,968 SLC16A1
    nsv5381058copy number variation1nstd102humanPathogenic GRCh37 chr1: 102,021,465-119,737,478 , GRCh38.p12 chr1: 101,555,909-119,194,855 AMYP1, MIR4256, 320 more genes
    nsv5363323translocation1nstd200human GRCh38 chr1: 112,933,607-112,933,607 , GRCh38 chr1: 112,916,825-112,916,825 , GRCh37.p13 chr1: 113,459,447-113,459,447 , GRCh37.p13 chr1: 113,476,229-113,476,229 SLC16A1
    nsv5353794translocation1nstd200human GRCh38 chr1: 112,910,838-112,910,838 , GRCh38 chr1: 112,910,922-112,910,922 , GRCh37.p13 chr1: 113,453,544-113,453,544 , GRCh37.p13 chr1: 113,453,460-113,453,460 SLC16A1
    nsv5353793translocation1nstd200human GRCh38 chr1: 112,908,653-112,908,653 , GRCh38 chr1: 112,911,778-112,911,778 , GRCh37.p13 chr1: 113,451,275-113,451,275 , GRCh37.p13 chr1: 113,454,400-113,454,400 SLC16A1
    nsv5338439translocation1nstd200human GRCh37 chr1: 113,459,447-113,459,447 , GRCh37 chr1: 113,476,229-113,476,229 , GRCh38.p12 chr1: 112,933,607-112,933,607 , GRCh38.p12 chr1|NW_009646196.1: 7,404-7,404 , GRCh38.p12 chr1: 112,916,825-112,916,825 , GRCh38.p12 chr1|NW_009646196.1: 24,186-24,186 SLC16A1
    nsv5286762copy number variation1nstd204human GRCh37.p13 chr1: 113,412,224-113,526,937 , GRCh38.p13 chr1: 112,869,602-112,984,315 SLC16A1, AKR7A2P1, 6 more genes
    nsv5212924copy number variation1nstd204human GRCh38.p13 chr1: 112,945,408-112,984,072 , GRCh37.p13 chr1: 113,488,030-113,526,694 SLC16A1, LOC107985189, 1 more genes
    nsv5208846copy number variation1nstd204human GRCh37.p13 chr1: 113,414,923-113,526,922 , GRCh38.p13 chr1: 112,872,301-112,984,300 SLC16A1, AKR7A2P1, 6 more genes
    nsv5190549mobile element insertion1nstd203human GRCh38 chr1: 112,930,865-112,930,879 , GRCh37.p13 chr1: 113,473,487-113,473,501 SLC16A1
    nsv5079318mobile element insertion1nstd203human GRCh38 chr1: 112,951,346-112,951,358 , GRCh37.p13 chr1: 113,493,968-113,493,980 SLC16A1
    nsv5063147mobile element insertion1nstd203human GRCh38 chr1: 112,934,672-112,934,687 , GRCh37.p13 chr1: 113,477,294-113,477,309 SLC16A1
    nsv4894420copy number variation1nstd200human GRCh38 chr1: 112,702,675-113,232,556 , GRCh37.p13 chr1: 113,245,297-113,775,178 RHOC, RPS19P2, 19 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