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 211

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6116985mobile element insertion1nstd186human GRCh37 chr20: 30,032,135-30,032,186 , GRCh38.p12 chr20: 31,444,332-31,444,383 DEFB123
    nsv5972438insertion1nstd209human GRCh38 chr20: 31,446,859-31,446,859 , GRCh37.p13 chr20: 30,034,662-30,034,662 DEFB123
    nsv5881750copy number variation1nstd209human GRCh38 chr20: 31,387,349-31,446,696 , GRCh37.p13 chr20: 29,975,152-30,034,499 DEFB121, DEFB119, 2 more genes
    nsv5709174mobile element insertion2nstd211human GRCh38 chr20: 31,444,332-31,444,332 , GRCh37.p13 chr20: 30,032,135-30,032,135 DEFB123
    nsv5668341insertion1nstd207human GRCh38 chr20: 31,444,314-31,444,314 , GRCh37.p13 chr20: 30,032,117-30,032,117 DEFB123
    nsv5431102mobile element insertion1nstd206human GRCh38 chr20: 31,444,332-31,444,383 , GRCh37.p13 chr20: 30,032,135-30,032,186 DEFB123
    nsv5284258copy number variation1nstd204human GRCh38.p13 chr20: 31,442,585-31,445,084 , GRCh37.p13 chr20: 30,030,388-30,032,887 DEFB123
    nsv5283549copy number variation1nstd204human GRCh38.p13 chr20: 31,227,801-32,548,400 , GRCh37.p13 chr20: 29,815,604-31,136,202 , XKR7, 52 more genes
    nsv5164660mobile element insertion1nstd203human GRCh38 chr20: 31,444,314-31,444,332 , GRCh37.p13 chr20: 30,032,117-30,032,135 DEFB123
    nsv5164260mobile element insertion1nstd203human GRCh38 chr20: 31,446,859-31,446,869 , GRCh37.p13 chr20: 30,034,662-30,034,672 DEFB123
    nsv5025504copy number variation1nstd200human GRCh38 chr20: 31,340,765-31,485,512 , GRCh37.p13 chr20: 29,928,568-30,073,315 RNA5SP480, DEFB118, 9 more genes
    nsv5025501copy number variation1nstd200human GRCh38 chr20: 31,308,012-31,715,091 , GRCh37.p13 chr20: 29,895,815-30,302,894 CD24P3, COX4I2, 24 more genes
    nsv4865520copy number variation1nstd200human GRCh37 chr20: 29,928,568-30,073,315 , GRCh38.p12 chr20: 31,340,765-31,485,512 DEFB122, DEFB119, 9 more genes
    nsv4729837copy number variation1nstd102humanLikely benign GRCh37 chr20: 29,833,534-30,494,851 , GRCh38.p12 chr20: 31,245,731-31,907,048 DEFB117, LOC105372588, 34 more genes
    nsv4729757copy number variation1nstd102humanLikely pathogenic GRCh37 chr20: 19,750,804-30,479,077 , GRCh38.p12 chr20: 19,770,160-31,891,274 BCL2L1, CD24P3, 222 more genes
    nsv4717025mobile element insertion1nstd186human GRCh37 chr20: 30,032,117-30,032,117 , GRCh38.p12 chr20: 31,444,314-31,444,314 DEFB123
    nsv4687633mobile element insertion1nstd186human GRCh37 chr20: 30,032,135-30,032,135 , GRCh38.p12 chr20: 31,444,332-31,444,332 DEFB123
    nsv4676397copy number variation1nstd102humanLikely benign GRCh37 chr20: 29,651,839-30,195,919 , GRCh38.p12 chr20: 30,417,163-31,608,116 MTCO3P32, RNU6-384P, 44 more genes
    nsv4633388copy number variation1nstd183human GRCh37 chr20: 29,989,493-30,053,536 , GRCh38.p12 chr20: 31,401,690-31,465,733 DEFB123, DEFB121, 2 more genes
    nsv4632642copy number variation1nstd183human GRCh37 chr20: 29,835,049-30,626,430 , GRCh38.p12 chr20: 31,247,246-32,038,627 DEFB122, HAUS6P2, 38 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