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 582

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6114838copy number variation1nstd186human GRCh37 chr20: 60,632,737-60,633,947 , GRCh38.p12 chr20: 62,057,681-62,058,891 TAF4
    nsv6112778copy number variation1nstd102humanPathogenic GRCh37 chr20: 51,799,648-62,916,626 , GRCh38.p12 chr20: 53,183,109-64,285,273 LINC01742, MTCO2P1, 253 more genes
    nsv5963191copy number variation1nstd209human GRCh38 chr20: 61,989,512-61,989,721 , GRCh37.p13 chr20: 60,564,568-60,564,777 TAF4
    nsv5959660copy number variation1nstd209human GRCh38 chr20: 62,049,837-62,049,889 , GRCh37.p13 chr20: 60,624,893-60,624,945 TAF4
    nsv5957782copy number variation1nstd209human GRCh38 chr20: 61,988,023-61,988,105 , GRCh37.p13 chr20: 60,563,079-60,563,161 TAF4
    nsv5957189copy number variation1nstd209human GRCh38 chr20: 61,995,568-61,995,886 , GRCh37.p13 chr20: 60,570,624-60,570,942 TAF4
    nsv5953932copy number variation1nstd209human GRCh38 chr20: 62,057,603-62,058,852 , GRCh37.p13 chr20: 60,632,659-60,633,908 TAF4
    nsv5951389copy number variation1nstd209human GRCh38 chr20: 61,984,538-61,984,676 , GRCh37.p13 chr20: 60,559,594-60,559,732 TAF4
    nsv5672213insertion1nstd207human GRCh38 chr20: 62,058,987-62,058,987 , GRCh37.p13 chr20: 60,634,043-60,634,043 TAF4
    nsv5672020insertion1nstd207human GRCh38 chr20: 61,982,202-61,982,202 , GRCh37.p13 chr20: 60,557,258-60,557,258 TAF4
    nsv5671759insertion1nstd207human GRCh38 chr20: 62,057,716-62,057,716 , GRCh37.p13 chr20: 60,632,772-60,632,772 TAF4
    nsv5671313insertion1nstd207human GRCh38 chr20: 62,057,634-62,057,634 , GRCh37.p13 chr20: 60,632,690-60,632,690 TAF4
    nsv5670280insertion1nstd207human GRCh38 chr20: 62,058,327-62,058,327 , GRCh37.p13 chr20: 60,633,383-60,633,383 TAF4
    nsv5670006insertion1nstd207human GRCh38 chr20: 62,055,262-62,055,262 , GRCh37.p13 chr20: 60,630,318-60,630,318 TAF4
    nsv5669795insertion2nstd207human GRCh38 chr20: 61,982,644-61,982,644 , GRCh37.p13 chr20: 60,557,700-60,557,700 TAF4
    nsv5669458insertion1nstd207human GRCh38 chr20: 61,981,794-61,981,794 , GRCh37.p13 chr20: 60,556,850-60,556,850 TAF4
    nsv5669455insertion1nstd207human GRCh38 chr20: 61,978,413-61,978,413 , GRCh37.p13 chr20: 60,553,469-60,553,469 TAF4
    nsv5668759insertion1nstd207human GRCh38 chr20: 61,985,959-61,985,959 , GRCh37.p13 chr20: 60,561,015-60,561,015 TAF4
    nsv5667673insertion1nstd207human GRCh38 chr20: 62,058,768-62,058,768 , GRCh37.p13 chr20: 60,633,824-60,633,824 TAF4
    nsv5666326insertion1nstd207human GRCh38 chr20: 61,982,097-61,982,097 , GRCh37.p13 chr20: 60,557,153-60,557,153 TAF4
    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