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 147

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5451525copy number variation1nstd206human GRCh38 chr3: 119,495,090-119,495,301 , GRCh37.p13 chr3: 119,213,937-119,214,148 POGLUT1
    nsv5450407copy number variation1nstd206human GRCh38 chr3: 119,490,648-119,492,251 , GRCh37.p13 chr3: 119,209,495-119,211,098 POGLUT1
    nsv5443560copy number variation1nstd206human GRCh38 chr3: 119,469,910-119,471,307 , GRCh37.p13 chr3: 119,188,757-119,190,154 POGLUT1
    nsv5089883mobile element insertion1nstd203human GRCh38 chr3: 119,467,607-119,467,625 , GRCh37.p13 chr3: 119,186,454-119,186,472 POGLUT1
    nsv5036857inversion1nstd200human GRCh38 chr3: 97,392,267-146,717,859 , GRCh37.p13 chr3: 97,111,111-146,435,646 , FBRSL1P1, 801 more genes
    nsv5031637inversion1nstd200human GRCh38 chr3: 112,181,184-125,673,487 , GRCh37.p13 chr3: 111,900,031-125,392,331 , ARHGAP31, 218 more genes
    nsv4683538copy number variation1nstd102humanLikely pathogenic GRCh37 chr3: 119,198,952-119,200,618 , GRCh38 chr3: 119,480,105-119,481,771 POGLUT1
    nsv4587181copy number variation1nstd183human GRCh37 chr3: 119,187,640-119,188,682 , GRCh38.p12 chr3: 119,468,793-119,469,835 POGLUT1
    nsv4560202mobile element insertion1nstd166human GRCh37.p13 chr3: 119,203,765-119,203,765 , GRCh38.p12 chr3: 119,484,918-119,484,918 POGLUT1
    nsv4468911mobile element insertion1nstd166human GRCh37.p13 chr3: 119,202,327-119,202,327 , GRCh38.p12 chr3: 119,483,480-119,483,480 POGLUT1
    nsv4317801inversion1nstd166human GRCh37.p13 chr3: 106,160,269-123,476,086 , GRCh38.p12 chr3: 106,441,422-123,757,239 , ADPRH, 270 more genes
    nsv3924082copy number variation1nstd102humanPathogenic NCBI36 chr3: 119,875,435-127,742,263 , GRCh38 chr3: 118,673,898-126,540,730 , GRCh37 chr3: 118,392,745-126,259,573 MYLK-AS2, RPL7AP11, 165 more genes
    nsv3923097copy number variation1nstd102humanPathogenic NCBI36 chr3: 120,318,703-127,122,267 , GRCh38 chr3: 119,117,166-125,920,734 , GRCh37 chr3: 118,836,013-125,639,577 POGLUT1, RN7SL397P, 141 more genes
    nsv3922717copy number variation1nstd102humanPathogenic NCBI36 chr3: 95,002,154-146,895,858 , GRCh38 chr3: 93,800,620-145,695,381 , GRCh37 chr3: 93,519,464-145,413,168 OR7E53P, HSPA8P9, 794 more genes
    nsv3919464copy number variation1nstd102humanPathogenic GRCh38 chr3: 114,122,562-124,532,374 , GRCh37 chr3: 113,841,409-124,251,221 , NCBI36 chr3: 115,324,099-125,733,911 B4GALT4-AS1, LSAMP, 144 more genes
    nsv3919094copy number variation1nstd102humanPathogenic GRCh37 chr3: 114,737,921-122,232,245 , GRCh38 chr3: 115,019,074-122,513,398 , NCBI36 chr3: 116,220,611-123,714,935 LOC105374054, CSTA, 106 more genes
    nsv3918981copy number variation1nstd102humanPathogenic GRCh37 chr3: 103,145,726-197,837,049 , GRCh38 chr3: 103,426,882-198,110,178 , NCBI36 chr3: 104,628,416-199,321,446 LINC02614, LINC02054, 1469 more genes
    nsv3918661copy number variation1nstd102humanPathogenic NCBI36 chr3: 95,088,205-124,418,220 , GRCh37 chr3: 93,605,515-122,935,530 , GRCh38 chr3: 93,886,671-123,216,683 MTCO2P29, GAP43, 401 more genes
    nsv3918094copy number variation1nstd102humanPathogenic NCBI36 chr3: 113,822,514-129,935,667 , GRCh38 chr3: 112,620,977-128,734,134 , GRCh37 chr3: 112,339,824-128,452,977 QTRT2, MIR544B, 284 more genes
    nsv3917839copy number variation1nstd102humanUncertain significance NCBI36 chr3: 119,046,495-122,028,158 , GRCh38 chr3: 117,844,958-120,826,621 , GRCh37 chr3: 117,563,805-120,545,468 ADPRH, HGD, 52 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