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 605

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7145672copy number variation1nstd232human GRCh37.p13 chr1: 7,923,045-7,923,119 , GRCh38.p12 chr1: 7,862,985-7,863,059 UTS2
    nsv7142705copy number variation1nstd232human GRCh37.p13 chr1: 7,924,948-7,925,057 , GRCh38.p12 chr1: 7,864,888-7,864,997 UTS2
    nsv7139908insertion1nstd232human GRCh37.p13 chr1: 7,916,657-7,916,657 , GRCh38.p12 chr1: 7,856,597-7,856,597 UTS2
    nsv7099175copy number variation1nstd231human GRCh38.p12 chr1: 6,492,665-9,894,222 , GRCh37 chr1: 6,552,725-9,954,280 RERE, CA6, 70 more genes
    nsv7098827copy number variation1nstd102humanPathogenic GRCh37 chr1: 4,481,271-20,530,242 , GRCh38.p12 chr1: 4,421,211-20,203,749 LOC107985467, LINC01777, 386 more genes
    nsv7096005copy number variation1nstd102humanUncertain significance GRCh37 chr1: 7,700,440-8,601,397 , GRCh38.p12 chr1: 7,640,380-8,541,338 RNU1-7P, PER3, 18 more genes
    nsv7058041inversion1nstd229human GRCh38 chr1: 1,845,355-9,534,096 , GRCh37.p13 chr1: 1,776,794-9,594,155 RPL37P9, TMEM52, 152 more genes
    nsv7057525inversion1nstd229human GRCh38 chr1: 7,829,944-15,116,659 , GRCh37.p13 chr1: 7,890,004-15,443,155 PEX14, RNU6-304P, 187 more genes
    nsv7056633inversion1nstd229human GRCh38 chr1: 7,835,759-7,844,713 , GRCh37.p13 chr1: 7,895,819-7,904,773 UTS2, PER3
    nsv7054534inversion1nstd229human GRCh38 chr1: 2,972,403-10,562,308 , GRCh37.p13 chr1: 2,888,967-10,622,365 RN7SL731P, LOC105376682, 145 more genes
    nsv7050952inversion1nstd229human GRCh38 chr1: 7,187,356-8,831,900 , GRCh37.p13 chr1: 7,247,416-8,891,959 RPL7P7, LOC107984915, 26 more genes
    nsv7047983inversion1nstd229human GRCh38 chr1: 5,346,988-12,521,611 , GRCh37.p13 chr1: 5,407,048-12,581,655 THAP3, UBIAD1, 165 more genes
    nsv7046461inversion1nstd229human GRCh38 chr1: 5,352,168-12,521,473 , GRCh37.p13 chr1: 5,412,228-12,581,517 LINC02606, C1orf127, 165 more genes
    nsv7044144inversion1nstd229human GRCh38 chr1: 6,762,728-10,175,549 , GRCh37.p13 chr1: 6,822,788-10,235,607 RPL7P11, LOC105376691, 68 more genes
    nsv7038365inversion1nstd229human GRCh38 chr1: 7,829,831-7,844,685 , GRCh37.p13 chr1: 7,889,891-7,904,745 PER3, UTS2
    nsv6655427copy number variation1nstd229human GRCh38 chr1: 7,903,751-7,911,901 , GRCh37.p13 chr1: 7,963,811-7,971,961 UTS2
    nsv6655266copy number variation1nstd229human GRCh38 chr1: 7,897,997-7,942,481 , GRCh37.p13 chr1: 7,958,057-8,002,541 TNFRSF9, UTS2, 1 more genes
    nsv6655240copy number variation1nstd229human GRCh38 chr1: 7,855,567-7,861,241 , GRCh37.p13 chr1: 7,915,627-7,921,301 UTS2
    nsv6655169copy number variation1nstd229human GRCh38 chr1: 7,855,101-7,859,806 , GRCh37.p13 chr1: 7,915,161-7,919,866 UTS2
    nsv6655157copy number variation1nstd229human GRCh38 chr1: 7,840,382-7,854,021 , GRCh37.p13 chr1: 7,900,442-7,914,081 UTS2, PER3
    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