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 529

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6711352copy number variation1nstd229human GRCh38 chr3: 38,170,212-38,173,860 , GRCh37.p13 chr3: 38,211,703-38,215,351 OXSR1
    nsv6703556copy number variation1nstd229human GRCh38 chr3: 38,226,966-38,229,102 , GRCh37.p13 chr3: 38,268,457-38,270,593 OXSR1
    nsv6674203copy number variation1nstd229human GRCh38 chr2: 19,349,168-19,350,311 , GRCh37.p13 chr2: 19,548,929-19,550,072 OSR1
    nsv7018844copy number variation1nstd229human GRCh38 chr20: 44,205,601-44,206,696 , GRCh37.p13 chr20: 42,834,241-42,835,336 OSER1
    nsv7030266copy number variation1nstd229human GRCh38 chr20: 44,203,186-44,203,234 , GRCh37.p13 chr20: 42,831,826-42,831,874 OSER1
    nsv6368877copy number variation1nstd223human GRCh38 chr3: 38,231,978-38,234,896 , GRCh37.p13 chr3: 38,273,469-38,276,387 OXSR1
    nsv6365125copy number variation1nstd223human GRCh38 chr3: 38,224,401-38,227,100 , GRCh37.p13 chr3: 38,265,892-38,268,591 OXSR1
    nsv6375343copy number variation1nstd223human GRCh38 chr3: 38,225,158-38,225,798 , GRCh37.p13 chr3: 38,266,649-38,267,289 OXSR1
    nsv6370483copy number variation1nstd223human GRCh38 chr3: 38,220,470-38,221,103 , GRCh37.p13 chr3: 38,261,961-38,262,594 OXSR1
    nsv6369896copy number variation1nstd223human GRCh38 chr3: 38,190,269-38,190,795 , GRCh37.p13 chr3: 38,231,760-38,232,286 OXSR1
    nsv6371781copy number variation1nstd223human GRCh38 chr3: 38,229,793-38,230,202 , GRCh37.p13 chr3: 38,271,284-38,271,693 OXSR1
    nsv6373584copy number variation1nstd223human GRCh38 chr3: 38,247,916-38,248,184 , GRCh37.p13 chr3: 38,289,407-38,289,675 OXSR1
    nsv5445221copy number variation1nstd206human GRCh38 chr3: 38,247,919-38,248,184 , GRCh37.p13 chr3: 38,289,410-38,289,675 OXSR1
    nsv5993829copy number variation1nstd212human GRCh38 chr3: 38,207,889-38,207,953 , GRCh37.p13 chr3: 38,249,380-38,249,444 OXSR1
    nsv4910842copy number variation1nstd200human GRCh38 chr3: 38,247,919-38,248,184 , GRCh37.p13 chr3: 38,289,410-38,289,675 OXSR1
    nsv4806617copy number variation1nstd200human GRCh37 chr3: 38,289,410-38,289,675 , GRCh38.p12 chr3: 38,247,919-38,248,184 OXSR1
    nsv4071695copy number variation1nstd166human GRCh37.p13 chr2: 19,548,928-19,550,071 , GRCh38.p12 chr2: 19,349,167-19,350,310 OSR1
    nsv4076549copy number variation1nstd166human GRCh37.p13 chr3: 38,275,460-38,276,522 , GRCh38.p12 chr3: 38,233,969-38,235,031 OXSR1
    esv3568700copy number variation1estd212human GRCh37 chr3: 38,242,356-38,281,995 , GRCh38.p12 chr3: 38,200,865-38,240,504 OXSR1
    esv3010151copy number variation1estd209human GRCh37 chr2: 19,554,150-19,554,158 , GRCh38.p12 chr2: 19,354,389-19,354,397 OSR1
    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