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 228

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112709copy number variation1nstd102humanPathogenic GRCh37 chr3: 123,000,000-129,700,000 , GRCh38.p12 chr3: 123,281,153-129,981,157 OR7E97P, MARK3P3, 160 more genes
    nsv6112688copy number variation1nstd102humanPathogenic GRCh37 chr3: 120,154,188-128,324,987 , GRCh38.p12 chr3: 120,435,341-128,606,144 RNU4-62P, MTCO1P29, 169 more genes
    nsv5957657insertion1nstd209human GRCh38 chr3: 126,637,932-126,637,932 , GRCh37.p13 chr3: 126,356,775-126,356,775 TXNRD3
    nsv5907435copy number variation1nstd209human GRCh38 chr3: 126,640,079-126,640,405 , GRCh37.p13 chr3: 126,358,922-126,359,248 TXNRD3
    nsv5888743copy number variation1nstd209human GRCh38 chr3: 126,642,244-126,645,744 , GRCh37.p13 chr3: 126,361,087-126,364,587 TXNRD3
    nsv5834638copy number variation1nstd209human GRCh38 chr3: 126,641,926-126,645,925 , GRCh37.p13 chr3: 126,360,769-126,364,768 TXNRD3
    nsv5690210mobile element insertion1nstd211human GRCh38 chr3: 126,617,849-126,617,849 , GRCh37.p13 chr3: 126,336,692-126,336,692 TXNRD3
    nsv5682048mobile element insertion1nstd211human GRCh38 chr3: 126,623,870-126,623,870 , GRCh37.p13 chr3: 126,342,713-126,342,713 METTL5P2, TXNRD3
    nsv5675945mobile element insertion1nstd211human GRCh38 chr3: 126,625,116-126,625,116 , GRCh37.p13 chr3: 126,343,959-126,343,959 TXNRD3, METTL5P2
    nsv5582877copy number variation1nstd207human GRCh38 chr3: 126,640,079-126,640,405 , GRCh37.p13 chr3: 126,358,922-126,359,248 TXNRD3
    nsv5435748copy number variation1nstd206human GRCh38 chr3: 126,640,095-126,640,406 , GRCh37.p13 chr3: 126,358,938-126,359,249 TXNRD3
    nsv5413798mobile element insertion1nstd206human GRCh38 chr3: 126,625,116-126,625,167 , GRCh37.p13 chr3: 126,343,959-126,344,010 METTL5P2, TXNRD3
    nsv5395574mobile element insertion1nstd206human GRCh38 chr3: 126,617,849-126,617,900 , GRCh37.p13 chr3: 126,336,692-126,336,743 TXNRD3
    nsv5383380mobile element deletion2nstd186human GRCh37 chr3: 126,358,938-126,359,249 , GRCh38.p12 chr3: 126,640,095-126,640,406 TXNRD3
    nsv5216162mobile element deletion1nstd204human GRCh38.p13 chr3: 126,640,095-126,640,406 , GRCh37.p13 chr3: 126,358,938-126,359,249 TXNRD3
    nsv5080195mobile element insertion1nstd203human GRCh38 chr3: 126,612,388-126,612,402 , GRCh37.p13 chr3: 126,331,231-126,331,245 TXNRD3
    nsv5036857inversion1nstd200human GRCh38 chr3: 97,392,267-146,717,859 , GRCh37.p13 chr3: 97,111,111-146,435,646 , FBRSL1P1, 801 more genes
    nsv4919964copy number variation1nstd200human GRCh38 chr3: 126,643,341-126,644,259 , GRCh37.p13 chr3: 126,362,184-126,363,102 TXNRD3
    nsv4919963copy number variation1nstd200human GRCh38 chr3: 126,610,711-126,615,081 , GRCh37.p13 chr3: 126,329,554-126,333,924 TXNRD3
    nsv4919962copy number variation1nstd200human GRCh38 chr3: 126,606,304-126,613,642 , GRCh37.p13 chr3: 126,325,147-126,332,485 TXNRD3
    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