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 4897

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6137802copy number variation1nstd102humanLikely pathogenic GRCh37 chrX: 32,827,600-32,841,514 , GRCh38.p12 chrX: 32,809,483-32,823,397 DMD
    nsv6137801copy number variation1nstd102humanLikely pathogenic GRCh37 chrX: 32,591,637-32,867,962 , GRCh38.p12 chrX: 32,573,520-32,849,845 DMD, MIR548F5, 1 more genes
    nsv6137800copy number variation1nstd102humanPathogenic GRCh37 chrX: 31,986,446-31,986,641 , GRCh38.p12 chrX: 31,968,329-31,968,524 DMD
    nsv6137797copy number variation1nstd102humanLikely pathogenic GRCh37 chrX: 32,717,411-33,229,674 , GRCh38.p12 chrX: 32,699,294-33,211,557 DMD, TBCAP1
    nsv6137777copy number variation1nstd102humanPathogenic GRCh37 chrX: 32,827,600-32,867,962 , GRCh38.p12 chrX: 32,809,483-32,849,845 DMD
    nsv6137776copy number variation1nstd102humanPathogenic GRCh37 chrX: 31,893,295-31,950,354 , GRCh38.p12 chrX: 31,875,178-31,932,237 DMD
    nsv6137774copy number variation1nstd102humanPathogenic GRCh37 chrX: 31,697,704-31,947,712 , GRCh38.p12 chrX: 31,679,587-31,929,595 DMD
    nsv6137766copy number variation1nstd102humanPathogenic GRCh37 chrX: 31,947,703-31,950,354 , GRCh38.p12 chrX: 31,929,586-31,932,237 DMD
    nsv6137765copy number variation1nstd102humanPathogenic GRCh37 chrX: 31,838,082-31,986,641 , GRCh38.p12 chrX: 31,819,965-31,968,524 DMD
    nsv6137764copy number variation1nstd102humanPathogenic GRCh37 chrX: 31,645,780-31,986,641 , GRCh38.p12 chrX: 31,627,663-31,968,524 DMD
    nsv6137763copy number variation1nstd102humanPathogenic GRCh37 chrX: 31,645,780-31,950,354 , GRCh38.p12 chrX: 31,627,663-31,932,237 DMD
    nsv6137762copy number variation1nstd102humanPathogenic GRCh37 chrX: 31,462,588-31,525,580 , GRCh38.p12 chrX: 31,444,471-31,507,463 DMD
    nsv6137738copy number variation1nstd102humanPathogenic GRCh37 chrX: 31,747,738-31,893,500 , GRCh38.p12 chrX: 31,729,621-31,875,383 DMD
    nsv6137737copy number variation1nstd102humanPathogenic GRCh37 chrX: 31,747,738-31,854,946 , GRCh38.p12 chrX: 31,729,621-31,836,829 DMD
    nsv6137665copy number variation1nstd102humanLikely pathogenic GRCh37 chrX: 31,496,492-31,893,304 , GRCh38.p12 chrX: 31,478,375-31,875,187 DMD
    nsv6137660copy number variation1nstd102humanPathogenic GRCh37 chrX: 32,509,636-32,827,609 , GRCh38.p12 chrX: 32,491,519-32,809,492 DMD, MIR548F5, 1 more genes
    nsv6130025mobile element insertion1nstd186human GRCh37 chrX: 32,379,301-32,379,352 , GRCh38.p12 chrX: 32,361,184-32,361,235 DMD
    nsv6127935insertion1nstd186human GRCh37 chrX: 32,103,669-32,103,719 , GRCh38.p12 chrX: 32,085,552-32,085,602 DMD
    nsv6127769insertion1nstd186human GRCh37 chrX: 31,470,360-31,470,397 , GRCh38.p12 chrX: 31,452,243-31,452,280 DMD
    nsv6127418insertion1nstd186human GRCh37 chrX: 32,722,409-32,722,409 , GRCh38.p12 chrX: 32,704,292-32,704,292 DMD
    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