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 877

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7051089inversion1nstd229human GRCh38 chr3: 23,497,025-23,499,416 , GRCh37.p13 chr3: 23,538,516-23,540,907 UBE2E2
    nsv7050177inversion1nstd229human GRCh38 chr3: 23,300,554-23,360,336 , GRCh37.p13 chr3: 23,342,045-23,401,827 UBE2E2
    nsv7048943inversion1nstd229human GRCh38 chr3: 23,378,911-23,382,680 , GRCh37.p13 chr3: 23,420,402-23,424,171 UBE2E2
    nsv7048921inversion1nstd229human GRCh38 chr3: 23,493,374-23,497,259 , GRCh37.p13 chr3: 23,534,865-23,538,750 UBE2E2
    nsv7042410inversion1nstd229human GRCh38 chr3: 23,211,515-23,214,522 , GRCh37.p13 chr3: 23,253,006-23,256,013 UBE2E2
    nsv7041966inversion1nstd229human GRCh38 chr3: 22,554,268-23,302,616 , GRCh37.p13 chr3: 22,595,759-23,344,107 RANP7, SALL4P5, 4 more genes
    nsv7040947inversion1nstd229human GRCh38 chr3: 23,392,779-23,392,794 , GRCh37.p13 chr3: 23,434,270-23,434,285 UBE2E2
    nsv6717342copy number variation1nstd229human GRCh38 chr3: 23,407,509-23,427,828 , GRCh37.p13 chr3: 23,449,000-23,469,319 UBE2E2
    nsv6717223copy number variation1nstd229human GRCh38 chr3: 23,211,764-23,212,255 , GRCh37.p13 chr3: 23,253,255-23,253,746 UBE2E2
    nsv6717103copy number variation1nstd229human GRCh38 chr3: 23,290,438-23,295,013 , GRCh37.p13 chr3: 23,331,929-23,336,504 UBE2E2
    nsv6716799copy number variation1nstd229human GRCh38 chr3: 23,318,601-23,322,300 , GRCh37.p13 chr3: 23,360,092-23,363,791 UBE2E2
    nsv6715888copy number variation1nstd229human GRCh38 chr3: 23,348,365-23,601,903 , GRCh37.p13 chr3: 23,389,856-23,643,394 UBE2E2
    nsv6715833copy number variation1nstd229human GRCh38 chr3: 23,278,892-23,281,810 , GRCh37.p13 chr3: 23,320,383-23,323,301 UBE2E2
    nsv6715549copy number variation1nstd229human GRCh38 chr3: 23,270,080-23,272,617 , GRCh37.p13 chr3: 23,311,571-23,314,108 UBE2E2
    nsv6715331copy number variation1nstd229human GRCh38 chr3: 23,413,351-23,418,729 , GRCh37.p13 chr3: 23,454,842-23,460,220 UBE2E2
    nsv6713789copy number variation1nstd229human GRCh38 chr3: 23,249,811-23,255,020 , GRCh37.p13 chr3: 23,291,302-23,296,511 UBE2E2
    nsv6713405copy number variation1nstd229human GRCh38 chr3: 23,226,477-23,235,757 , GRCh37.p13 chr3: 23,267,968-23,277,248 UBE2E2
    nsv6713114copy number variation1nstd229human GRCh38 chr3: 23,506,059-23,506,087 , GRCh37.p13 chr3: 23,547,550-23,547,578 UBE2E2
    nsv6713002copy number variation1nstd229human GRCh38 chr3: 23,455,036-23,455,058 , GRCh37.p13 chr3: 23,496,527-23,496,549 UBE2E2
    nsv6712654copy number variation1nstd229human GRCh38 chr3: 23,256,030-23,259,012 , GRCh37.p13 chr3: 23,297,521-23,300,503 UBE2E2
    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