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 381

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5718259mobile element insertion1nstd211human GRCh38 chr1: 113,131,935-113,131,935 , GRCh37.p13 chr1: 113,674,557-113,674,557 LRIG2
    nsv5717251mobile element insertion1nstd211human GRCh38 chr1: 113,078,348-113,078,348 , GRCh37.p13 chr1: 113,620,970-113,620,970 LRIG2
    nsv5717181mobile element insertion2nstd211human GRCh38 chr1: 113,077,539-113,077,539 , GRCh37.p13 chr1: 113,620,161-113,620,161 LRIG2
    nsv5680397mobile element insertion1nstd211human GRCh38 chr1: 113,084,629-113,084,629 , GRCh37.p13 chr1: 113,627,251-113,627,251 LRIG2
    nsv5673149copy number variation1nstd102humanPathogenic GRCh37 chr1: 113,636,961-113,653,184 , GRCh38.p12 chr1: 113,094,339-113,110,562 LRIG2
    nsv5613056insertion1nstd207human GRCh38 chr1: 113,077,521-113,077,521 , GRCh37.p13 chr1: 113,620,143-113,620,143 LRIG2
    nsv5554787mobile element insertion1nstd206human GRCh38 chr1: 113,131,935-113,131,986 , GRCh37.p13 chr1: 113,674,557-113,674,608 LRIG2
    nsv5431006copy number variation1nstd206human GRCh38 chr1: 113,097,541-113,098,774 , GRCh37.p13 chr1: 113,640,163-113,641,396 LRIG2
    nsv5429360copy number variation1nstd206human GRCh38 chr1: 111,687,835-115,150,000 , GRCh37.p13 chr1: 112,230,457-115,692,621 , ST7L, 77 more genes
    nsv5428108copy number variation1nstd206human GRCh38 chr1: 113,068,697-113,071,175 , GRCh37.p13 chr1: 113,611,319-113,613,797 LRIG2, LRIG2-DT
    nsv5427216copy number variation1nstd206human GRCh38 chr1: 113,076,177-113,078,401 , GRCh37.p13 chr1: 113,618,799-113,621,023 LRIG2
    nsv5426029copy number variation1nstd206human GRCh38 chr1: 113,079,930-113,080,991 , GRCh37.p13 chr1: 113,622,552-113,623,613 LRIG2
    nsv5415158copy number variation1nstd206human GRCh38 chr1: 113,095,019-113,097,844 , GRCh37.p13 chr1: 113,637,641-113,640,466 LRIG2
    nsv5414972copy number variation1nstd206human GRCh38 chr1: 113,121,651-113,123,311 , GRCh37.p13 chr1: 113,664,273-113,665,933 LRIG2
    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
    nsv5284378copy number variation1nstd204human GRCh38.p13 chr1: 113,086,253-113,087,533 , GRCh37.p13 chr1: 113,628,875-113,630,155 LRIG2
    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
    nsv4894419copy number variation1nstd200human GRCh38 chr1: 112,670,692-113,135,319 , GRCh37.p13 chr1: 113,213,314-113,677,941 CAPZA1, SLC16A1-AS1, 17 more genes
    nsv4894418copy number variation1nstd200human GRCh38 chr1: 112,549,341-113,353,065 , GRCh37.p13 chr1: 113,091,963-113,895,687 LOC105378911, RNU7-70P, 23 more genes
    nsv4890846copy number variation1nstd200human GRCh38 chr1: 113,121,476-113,121,596 , GRCh37.p13 chr1: 113,664,098-113,664,218 LRIG2
    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