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 356

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6126420insertion1nstd186human GRCh37 chr3: 13,723,589-13,723,625 , GRCh38.p12 chr3: 13,682,090-13,682,126 LINC00620
    nsv5964570insertion1nstd209human GRCh38 chr3: 13,727,404-13,727,404 , GRCh37.p13 chr3: 13,768,902-13,768,902 LINC00620
    nsv5955103insertion1nstd209human GRCh38 chr3: 13,682,078-13,682,078 , GRCh37.p13 chr3: 13,723,577-13,723,577 LINC00620
    nsv5902980copy number variation1nstd209human GRCh38 chr3: 13,714,478-13,714,536 , GRCh37.p13 chr3: 13,755,977-13,756,035 LINC00620
    nsv5897122copy number variation1nstd209human GRCh38 chr3: 13,711,748-13,711,809 , GRCh37.p13 chr3: 13,753,247-13,753,308 LINC00620
    nsv5693787mobile element insertion2nstd211human GRCh38 chr3: 13,727,417-13,727,417 , GRCh37.p13 chr3: 13,768,915-13,768,915 LINC00620
    nsv5622521insertion1nstd207human GRCh38 chr3: 13,682,077-13,682,077 , GRCh37.p13 chr3: 13,723,576-13,723,576 LINC00620
    nsv5619317insertion1nstd207human GRCh38 chr3: 13,711,750-13,711,750 , GRCh37.p13 chr3: 13,753,249-13,753,249 LINC00620
    nsv5606722insertion1nstd207human GRCh38 chr3: 13,679,601-13,679,601 , GRCh37.p13 chr3: 13,721,100-13,721,100 LINC00620
    nsv5581095copy number variation1nstd207human GRCh38 chr3: 13,714,478-13,714,536 , GRCh37.p13 chr3: 13,755,977-13,756,035 LINC00620
    nsv5576202copy number variation1nstd207human GRCh38 chr3: 13,664,776-13,668,893 , GRCh37.p13 chr3: 13,706,276-13,710,393 LINC00620
    nsv5544502insertion1nstd206human GRCh38 chr3: 13,682,090-13,682,126 , GRCh37.p13 chr3: 13,723,589-13,723,625 LINC00620
    nsv5538315insertion1nstd206human GRCh38 chr3: 13,708,614-13,708,618 , GRCh37.p13 chr3: 13,750,113-13,750,117 LINC00620
    nsv5447245copy number variation1nstd206human GRCh38 chr3: 13,577,068-13,677,602 , GRCh37.p13 chr3: 13,618,568-13,719,101 FBLN2, LINC00620, 2 more genes
    nsv5447056copy number variation1nstd206human GRCh38 chr3: 13,708,551-13,708,823 , GRCh37.p13 chr3: 13,750,050-13,750,322 LINC00620
    nsv5442547copy number variation1nstd206human GRCh38 chr3: 13,682,046-13,682,136 , GRCh37.p13 chr3: 13,723,545-13,723,635 LINC00620
    nsv5436601copy number variation1nstd206human GRCh38 chr3: 13,664,779-13,668,894 , GRCh37.p13 chr3: 13,706,279-13,710,394 LINC00620
    nsv5434775copy number variation1nstd206human GRCh38 chr3: 13,718,589-13,718,647 , GRCh37.p13 chr3: 13,760,088-13,760,146 LINC00620
    nsv5351459translocation1nstd200human GRCh38 chr3: 13,668,894-13,668,894 , GRCh38 chr3: 13,664,779-13,664,779 , GRCh37.p13 chr3: 13,706,279-13,706,279 , GRCh37.p13 chr3: 13,710,394-13,710,394 LINC00620
    nsv5339140translocation1nstd200human GRCh37 chr3: 13,710,394-13,710,394 , GRCh37 chr3: 13,706,279-13,706,279 , GRCh38.p12 chr3: 13,664,779-13,664,779 , GRCh38.p12 chr3: 13,668,894-13,668,894 LINC00620
    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