U.S. flag

An official website of the United States government

Format
Items per page

Send to:

Choose Destination

Links from OMIM

Items: 9

    loading data ...

    Number of Variants: 9

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5564523delins1nstd102humanPathogenic GRCh38 chr9: 34,648,944-34,651,238 , GRCh37 chr9: 34,648,941-34,651,235 GALT, IL11RA
    nsv4684120copy number variation1nstd102humanPathogenic GRCh37 chr9: 34,645,661-34,648,822 , GRCh38 chr9: 34,645,664-34,648,825 GALT
    nsv4681850copy number variation1nstd102humanPathogenic GRCh37 chr9: 34,645,556-34,649,571 , GRCh38.p12 chr9: 34,645,559-34,649,574 GALT
    nsv4681838copy number variation1nstd102humanPathogenic GRCh37 chr9: 34,645,556-34,648,911 , GRCh38.p12 chr9: 34,645,559-34,648,914 GALT
    nsv4578507copy number variation1nstd102humanPathogenic GRCh37 chr9: 34,647,752-34,649,645 , GRCh38 chr9: 34,647,755-34,649,648 GALT
    nsv4452581copy number variation1nstd102humanPathogenic GRCh37 chr9: 34,646,606-34,650,456 , GRCh38 chr9: 34,646,609-34,650,459 IL11RA, GALT
    nsv3876480copy number variation1nstd102humanPathogenic GRCh38 chr9: 34,646,586-34,651,238 , GRCh37 chr9: 34,646,583-34,651,235 IL11RA, GALT
    nsv3872341copy number variation1nstd102humanPathogenic GRCh37 chr9: 34,645,556-34,651,235 , GRCh38 chr9: 34,645,559-34,651,238 IL11RA, GALT
    nsv1398540copy number variation1nstd102humanPathogenic GRCh38 chr9: 34,644,530-34,653,250 , GRCh37 chr9: 34,644,527-34,653,247 GALT, IL11RA
    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