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 699

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7073193inversion1nstd229human GRCh38 chr12: 85,088,396-85,098,268 , GRCh37.p13 chr12: 85,482,174-85,492,046 LRRIQ1
    nsv7068058inversion1nstd229human GRCh38 chr12: 83,660,778-85,331,040 , GRCh37.p13 chr12: 84,054,557-85,724,818 TSPAN19, LINC02820, 7 more genes
    nsv7065990inversion1nstd229human GRCh38 chr12: 85,163,188-85,163,234 , GRCh37.p13 chr12: 85,556,966-85,557,012 LRRIQ1
    nsv7060577inversion1nstd229human GRCh38 chr12: 85,273,261-85,409,719 , GRCh37.p13 chr12: 85,667,039-85,803,497 ALX1, LRRIQ1, 1 more genes
    nsv6937991copy number variation1nstd229human GRCh38 chr12: 85,127,647-85,238,687 , GRCh37.p13 chr12: 85,521,425-85,632,465 LRRIQ1
    nsv6937864copy number variation1nstd229human GRCh38 chr12: 85,065,995-85,067,174 , GRCh37.p13 chr12: 85,459,773-85,460,952 LRRIQ1
    nsv6937133copy number variation1nstd229human GRCh38 chr12: 85,162,113-85,206,717 , GRCh37.p13 chr12: 85,555,891-85,600,495 LRRIQ1
    nsv6937014copy number variation1nstd229human GRCh38 chr12: 85,067,528-85,067,957 , GRCh37.p13 chr12: 85,461,306-85,461,735 LRRIQ1
    nsv6936892copy number variation1nstd229human GRCh38 chr12: 85,164,637-85,171,254 , GRCh37.p13 chr12: 85,558,415-85,565,032 LRRIQ1
    nsv6935711copy number variation1nstd229human GRCh38 chr12: 85,220,555-85,228,476 , GRCh37.p13 chr12: 85,614,333-85,622,254 LRRIQ1
    nsv6935704copy number variation1nstd229human GRCh38 chr12: 85,218,501-85,224,807 , GRCh37.p13 chr12: 85,612,279-85,618,585 LRRIQ1
    nsv6934324copy number variation1nstd229human GRCh38 chr12: 85,189,601-85,191,000 , GRCh37.p13 chr12: 85,583,379-85,584,778 LRRIQ1
    nsv6933897copy number variation1nstd229human GRCh38 chr12: 85,154,639-85,322,708 , GRCh37.p13 chr12: 85,548,417-85,716,486 ALX1, LINC02820, 1 more genes
    nsv6932746copy number variation1nstd229human GRCh38 chr12: 85,247,201-85,250,400 , GRCh37.p13 chr12: 85,640,979-85,644,178 LRRIQ1
    nsv6931766copy number variation1nstd229human GRCh38 chr12: 85,265,332-85,279,028 , GRCh37.p13 chr12: 85,659,110-85,672,806 ALX1, LRRIQ1
    nsv6931628copy number variation1nstd229human GRCh38 chr12: 85,057,373-85,057,481 , GRCh37.p13 chr12: 85,451,151-85,451,259 LRRIQ1
    nsv6931383copy number variation1nstd229human GRCh38 chr12: 85,080,468-85,303,526 , GRCh37.p13 chr12: 85,474,246-85,697,304 ALX1, LRRIQ1
    nsv6931036copy number variation1nstd229human GRCh38 chr12: 85,109,795-85,121,054 , GRCh37.p13 chr12: 85,503,573-85,514,832 LRRIQ1
    nsv6930146copy number variation1nstd229human GRCh38 chr12: 85,244,609-85,293,157 , GRCh37.p13 chr12: 85,638,387-85,686,935 ALX1, LRRIQ1
    nsv6929794copy number variation1nstd229human GRCh38 chr12: 85,079,672-85,082,906 , GRCh37.p13 chr12: 85,473,450-85,476,684 LRRIQ1
    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