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 6315

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6126027insertion1nstd186human GRCh37 chr8: 1,285,586-1,285,586 , GRCh38.p12 chr8|NT_187565.1: 56,636-56,636 , GRCh38.p12 chr8: 1,337,420-1,337,420 DLGAP2
    nsv6123093copy number variation1nstd186human GRCh37 chr8: 1,299,174-1,300,447 , GRCh38.p12 chr8: 1,351,008-1,352,281 , GRCh38.p12 chr8|NT_187565.1: 70,224-71,497 DLGAP2
    nsv6122957copy number variation1nstd186human GRCh37 chr8: 1,185,702-1,185,964 , GRCh38.p12 chr8: 1,235,702-1,235,964 DLGAP2
    nsv6122426copy number variation1nstd186human GRCh37 chr8: 973,585-973,643 , GRCh38.p12 chr8|NT_187568.1: 164,875-164,933 , GRCh38.p12 chr8: 1,023,585-1,023,643 DLGAP2
    nsv6121609copy number variation1nstd186human GRCh37 chr8: 1,333,472-1,333,844 , GRCh38.p12 chr8|NT_187565.1: 104,765-105,079 , GRCh38.p12 chr8: 1,385,306-1,385,678 DLGAP2
    nsv5967382insertion1nstd209human GRCh38 chr8: 1,344,128-1,344,128 , GRCh37.p13 chr8: 1,292,294-1,292,294 DLGAP2
    nsv5966625insertion1nstd209human GRCh38 chr8: 1,256,571-1,256,571 , GRCh37.p13 chr8: 1,206,571-1,206,571 DLGAP2
    nsv5966213insertion1nstd209human GRCh38 chr8: 1,267,570-1,267,570 , GRCh37.p13 chr8: 1,217,570-1,217,570 DLGAP2
    nsv5964613insertion1nstd209human GRCh38 chr8: 881,667-881,667 , GRCh37.p13 chr8: 831,667-831,667 , DLGAP2, 1 more genes
    nsv5963355insertion1nstd209human GRCh38 chr8: 1,491,053-1,491,053 , GRCh37.p13 chr8: 1,439,219-1,439,219 DLGAP2
    nsv5962808insertion1nstd209human GRCh38 chr8: 960,237-960,237 , GRCh37.p13 chr8: 910,237-910,237 DLGAP2
    nsv5962392insertion1nstd209human GRCh38 chr8: 1,227,155-1,227,155 , GRCh37.p13 chr8: 1,177,155-1,177,155 DLGAP2
    nsv5961411insertion1nstd209human GRCh38 chr8: 1,349,367-1,349,367 , GRCh37.p13 chr8: 1,297,533-1,297,533 DLGAP2
    nsv5959707insertion1nstd209human GRCh38 chr8: 1,337,418-1,337,418 , GRCh37.p13 chr8: 1,285,584-1,285,584 DLGAP2
    nsv5959587insertion1nstd209human GRCh38 chr8: 1,362,358-1,362,358 , GRCh37.p13 chr8: 1,310,524-1,310,524 DLGAP2
    nsv5956435insertion1nstd209human GRCh38 chr8: 1,417,689-1,417,689 , GRCh37.p13 chr8: 1,365,855-1,365,855 DLGAP2
    nsv5955713insertion1nstd209human GRCh38 chr8: 1,456,806-1,456,806 , GRCh37.p13 chr8: 1,404,972-1,404,972 DLGAP2
    nsv5955355insertion1nstd209human GRCh38 chr8: 1,417,151-1,417,151 , GRCh37.p13 chr8: 1,365,317-1,365,317 DLGAP2
    nsv5954893insertion1nstd209human GRCh38 chr8: 1,460,757-1,460,757 , GRCh37.p13 chr8: 1,408,923-1,408,923 DLGAP2
    nsv5952315insertion1nstd209human GRCh38 chr8: 1,491,397-1,491,397 , GRCh37.p13 chr8: 1,439,563-1,439,563 DLGAP2
    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