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 376

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7144457insertion1nstd232human GRCh37.p13 chr3: 145,797,043-145,797,043 , GRCh38.p12 chr3: 146,079,256-146,079,256 PLOD2
    nsv7143652insertion1nstd232human GRCh37.p13 chr3: 145,806,497-145,806,497 , GRCh38.p12 chr3: 146,088,710-146,088,710 PLOD2
    nsv7142704insertion1nstd232human GRCh37.p13 chr3: 145,806,500-145,806,500 , GRCh38.p12 chr3: 146,088,713-146,088,713 PLOD2
    nsv7138239insertion1nstd232human GRCh37.p13 chr3: 145,797,044-145,797,044 , GRCh38.p12 chr3: 146,079,257-146,079,257 PLOD2
    nsv7096541copy number variation1nstd102humanUncertain significance GRCh37 chr3: 145,788,504-145,878,776 , GRCh38.p12 chr3: 146,070,717-146,160,989 PLOD2
    nsv7045074inversion1nstd229human GRCh38 chr3: 146,126,804-146,130,301 , GRCh37.p13 chr3: 145,844,591-145,848,088 PLOD2
    nsv7042992inversion1nstd229human GRCh38 chr3: 145,930,119-146,730,530 , GRCh37.p13 chr3: 145,647,906-146,448,317 PLSCR2, LNCSRLR, 8 more genes
    nsv6738033copy number variation1nstd229human GRCh38 chr3: 146,138,900-146,141,475 , GRCh37.p13 chr3: 145,856,687-145,859,262 PLOD2
    nsv6731575copy number variation1nstd229human GRCh38 chr3: 146,146,701-146,156,600 , GRCh37.p13 chr3: 145,864,488-145,874,387 PLOD2
    nsv6730938copy number variation1nstd229human GRCh38 chr3: 146,072,181-146,073,126 , GRCh37.p13 chr3: 145,789,968-145,790,913 PLOD2
    nsv6730887copy number variation1nstd229human GRCh38 chr3: 146,148,038-146,148,093 , GRCh37.p13 chr3: 145,865,825-145,865,880 PLOD2
    nsv6729269copy number variation1nstd229human GRCh38 chr3: 146,128,715-146,128,776 , GRCh37.p13 chr3: 145,846,502-145,846,563 PLOD2
    nsv6727008copy number variation1nstd229human GRCh38 chr3: 142,255,714-146,323,295 , GRCh37.p13 chr3: 141,974,556-146,041,082 LOC105374142, XRN1, 44 more genes
    nsv6725590copy number variation1nstd229human GRCh38 chr3: 146,153,708-146,157,801 , GRCh37.p13 chr3: 145,871,495-145,875,588 PLOD2
    nsv6724755copy number variation1nstd229human GRCh38 chr3: 146,033,784-146,176,040 , GRCh37.p13 chr3: 145,751,571-145,893,827 LOC105374145, PLOD2, 1 more genes
    nsv6723621copy number variation1nstd229human GRCh38 chr3: 146,141,494-146,147,577 , GRCh37.p13 chr3: 145,859,281-145,865,364 PLOD2
    nsv6722370copy number variation1nstd229human GRCh38 chr3: 146,102,166-146,103,771 , GRCh37.p13 chr3: 145,819,953-145,821,558 PLOD2
    nsv6719663copy number variation1nstd229human GRCh38 chr3: 146,137,762-146,193,593 , GRCh37.p13 chr3: 145,855,549-145,911,380 LOC105374145, PLOD2, 1 more genes
    nsv6637156copy number variation1nstd102humanPathogenic GRCh37 chr3: 116,620,308-172,042,292 , GRCh38.p12 chr3: 116,901,461-172,324,502 H1-10, AADACL2-AS1, 846 more genes
    nsv6636825copy number variation1nstd102humanUncertain significance GRCh37 chr3: 145,694,358-146,217,695 , GRCh38.p12 chr3: 145,976,571-146,499,908 PLSCR4, PLOD2, 4 more genes
    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