U.S. flag

An official website of the United States government

Format
Items per page

Send to:

Choose Destination

Search results

Items: 1 to 20 of 173

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7098523copy number variation1nstd102humanPathogenic GRCh37 chrX: 38,132,619-38,164,063 , GRCh38.p12 chrX: 38,273,366-38,304,810 RPGR
    nsv4348351copy number variation1nstd102humanPathogenic GRCh37 chrX: 38,144,822-38,164,037 , GRCh38.p12 chrX: 38,285,569-38,304,784 RPGR
    nsv7148197copy number variation1nstd102humanPathogenic GRCh38 chrX: 38,269,073-38,287,133 , GRCh37.p13 chrX: 38,128,326-38,146,386 RPGR
    nsv7148193copy number variation1nstd102humanPathogenic GRCh38 chrX: 38,297,187-38,299,239 , GRCh37.p13 chrX: 38,156,440-38,158,492 RPGR
    nsv4685694copy number variation1nstd102humanPathogenic GRCh38 chrX: 38,315,735-38,317,538 , GRCh37 chrX: 38,174,988-38,176,791 RPGR
    nsv7098527copy number variation1nstd102humanPathogenic GRCh37 chrX: 38,182,086-38,182,797 , GRCh38.p12 chrX: 38,322,833-38,323,544 RPGR
    nsv7098412copy number variation1nstd102humanPathogenic GRCh37 chrX: 38,160,137-38,160,644 , GRCh38.p12 chrX: 38,300,884-38,301,391 RPGR
    nsv7148183copy number variation1nstd102humanPathogenic GRCh38 chrX: 38,301,150-38,301,469 , GRCh37.p13 chrX: 38,160,403-38,160,722 RPGR
    nsv7098525copy number variation1nstd102humanPathogenic GRCh37 chrX: 38,150,626-38,150,757 , GRCh38.p12 chrX: 38,291,373-38,291,504 RPGR
    nsv6315329copy number variation1nstd102humanPathogenic GRCh38 chrX: 38,317,307-38,317,363 , GRCh37 chrX: 38,176,560-38,176,616 RPGR
    nsv6636082copy number variation1nstd102humanPathogenic GRCh37 chrX: 38,146,038-38,146,039 , GRCh38 chrX: 38,286,785-38,286,786 RPGR
    nsv6137732copy number variation1nstd102humanPathogenic GRCh37 chrX: 38,146,103-38,146,104 , GRCh38 chrX: 38,286,850-38,286,851 RPGR
    nsv7093571insertion1nstd102humanPathogenic GRCh37 chrX: 38,145,378-38,145,378 , GRCh38 chrX: 38,286,125-38,286,125 RPGR
    nsv7098524copy number variation1nstd102humanUncertain significance GRCh37 chrX: 38,146,328-38,150,297 , GRCh38.p12 chrX: 38,287,075-38,291,044 RPGR
    nsv7093093copy number variation1nstd102humanUncertain significance GRCh37 chrX: 38,145,346-38,145,447 , GRCh38 chrX: 38,286,093-38,286,194 RPGR
    nsv4683215copy number variation1nstd102humanUncertain significance GRCh37 chrX: 38,128,859-38,170,046 , GRCh38.p12 chrX: 38,269,606-38,310,793 RPGR
    nsv7098526copy number variation1nstd102humanUncertain significance GRCh37 chrX: 38,169,848-38,182,797 , GRCh38.p12 chrX: 38,310,595-38,323,544 RPGR
    nsv4682224copy number variation1nstd102humanUncertain significance GRCh37 chrX: 38,128,859-38,129,105 , GRCh38.p12 chrX: 38,269,606-38,269,852 RPGR
    nsv7098976copy number variation1nstd102humanUncertain significance GRCh38 chrX: 38,286,519-38,286,520 , GRCh37 chrX: 38,145,772-38,145,773 RPGR
    nsv7093312copy number variation1nstd102humanUncertain significance GRCh38 chrX: 38,286,179-38,286,180 , GRCh37 chrX: 38,145,432-38,145,433 RPGR
    Format
    Items per page

    Send to:

    Choose Destination

    Supplemental Content

    Filters: Manage Filters

    Find related data

    Search details

    See more...

    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