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 694

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5959252copy number variation1nstd209human GRCh38 chr22: 22,031,472-22,168,098 , GRCh37.p13 chr22: 22,385,870-22,522,491 IGLVI-68, IGLV4-69, 15 more genes
    nsv5959042copy number variation1nstd209human GRCh38 chr22: 22,026,551-22,904,986 , GRCh37.p13 chr22: 22,380,949-23,247,166 , IGLV1-44, 113 more genes
    nsv5957865copy number variation1nstd209human GRCh38 chr22: 22,031,459-22,893,783 , GRCh37.p13 chr22: 22,385,857-23,235,963 , IGLV7-46, 108 more genes
    nsv5953877copy number variation1nstd209human GRCh38 chr22: 22,031,467-22,899,623 , GRCh37.p13 chr22: 22,385,865-23,241,803 , LOC100419915, 110 more genes
    nsv5952603copy number variation1nstd209human GRCh38 chr22: 22,026,550-22,899,617 , GRCh37.p13 chr22: 22,380,948-23,241,797 , VPREB1, 111 more genes
    nsv5949766copy number variation1nstd209human GRCh38 chr22: 22,026,550-22,893,779 , GRCh37.p13 chr22: 22,380,948-23,235,959 , IGLV2-5, 109 more genes
    nsv5947607copy number variation1nstd209human GRCh38 chr22: 22,031,465-22,904,986 , GRCh37.p13 chr22: 22,385,863-23,247,166 , IGLV3-15, 112 more genes
    nsv5882065copy number variation2nstd209human GRCh38 chr22: 22,056,761-22,063,826 , GRCh37.p13 chr22: 22,411,174-22,418,241 IGL, IGLVIV-66-1, 1 more genes
    nsv5878629copy number variation2nstd209human GRCh38 chr22: 22,051,731-22,062,526 , GRCh37.p13 chr22: 22,406,129-22,416,941 IGLVV-66, IGL, 1 more genes
    nsv5871399copy number variation2nstd209human GRCh38 chr22: 22,050,578-22,058,660 , GRCh37.p13 chr22: 22,404,976-22,413,072 IGLVIV-66-1, IGL
    nsv5546749copy number variation1nstd206human GRCh38 chr22: 21,955,564-22,271,564 , GRCh37.p13 chr22: 22,309,936-22,625,947 IGLVI-68, IGLV11-55, 29 more genes
    nsv5299274copy number variation1nstd204human GRCh38.p13 chr22: 21,958,001-22,115,000 , GRCh37.p13 chr22: 22,312,373-22,469,392 IGLVIV-64, IGLVIV-66-1, 14 more genes
    nsv5200375copy number variation1nstd102humanLikely pathogenic GRCh37 chr22: 22,313,128-22,556,733 , GRCh38.p12 chr22: 21,958,756-22,202,339 IGL, TOP3B, 24 more genes
    nsv5038987copy number variation1nstd200human GRCh38 chr22: 22,031,471-22,918,164 , GRCh37.p13 chr22: 22,385,869-23,260,336 , IGLV1-44, 119 more genes
    nsv5030354copy number variation1nstd200human GRCh38 chr22: 22,026,546-22,893,790 , GRCh37.p13 chr22: 22,380,944-23,235,970 , IGLV3-27, 109 more genes
    nsv4869101copy number variation1nstd200human GRCh37 chr22: 22,385,869-23,260,336 , GRCh38.p12 chr22: 22,031,471-22,918,164 , ZNF280A, 119 more genes
    nsv4869100copy number variation1nstd200human GRCh37 chr22: 22,385,866-23,235,964 , GRCh38.p12 chr22: 22,031,468-22,893,784 , IGLVV-58, 108 more genes
    nsv4869099copy number variation1nstd200human GRCh37 chr22: 22,380,950-23,247,167 , GRCh38.p12 chr22: 22,026,552-22,904,987 , BCRP4, 113 more genes
    nsv4869098copy number variation1nstd200human GRCh37 chr22: 22,380,944-23,235,970 , GRCh38.p12 chr22: 22,026,546-22,893,790 , LOC102724638, 109 more genes
    nsv4768383copy number variation1nstd102humanPathogenic GRCh37 chr22: 16,888,899-26,483,608 , GRCh38.p12 chr22: 16,408,173-26,087,642 KRT18P62, LOC101060852, 437 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