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 137

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7043003inversion1nstd229human GRCh38 chr3: 152,267,064-152,267,175 , GRCh37.p13 chr3: 151,984,853-151,984,964 MBNL1-AS1, MBNL1
    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
    nsv6313678copy number variation1nstd102humanPathogenic GRCh37 chr3: 145,486,960-160,504,834 , GRCh38.p12 chr3: 145,769,173-160,787,046 RNU6-901P, RPL32P8, 229 more genes
    nsv6313632copy number variation1nstd102humanUncertain significance GRCh37 chr3: 151,147,204-154,845,718 , GRCh38.p12 chr3: 151,429,416-155,127,929 LOC105374171, ARHGEF26-AS1, 42 more genes
    nsv6290273copy number variation1nstd102humanPathogenic GRCh37 chr3: 142,729,607-157,921,084 , GRCh38.p12 chr3: 143,010,765-158,203,295 LINC02066, TM4SF1-AS1, 206 more genes
    nsv6290244copy number variation1nstd102humanPathogenic GRCh37 chr3: 143,439,359-165,252,122 , GRCh38.p12 chr3: 143,720,517-165,534,334 LOC102724145, C3orf80, 273 more genes
    nsv6134674copy number variation1nstd213human GRCh37 chr3: 150,600,000-153,170,001 , GRCh38.p12 chr3: 150,882,213-153,452,212 CLRN1-AS1, MBNL1-AS1, 37 more genes
    nsv5835281copy number variation1nstd209human GRCh38 chr3: 152,269,933-152,270,955 , GRCh37.p13 chr3: 151,987,722-151,988,744 MBNL1-AS1, MBNL1
    nsv5381765copy number variation1nstd102humanPathogenic GRCh37 chr3: 138,173,683-162,494,699 , GRCh38.p12 chr3: 138,454,841-162,776,911 MBNL1-AS1, LOC107986138, 339 more genes
    nsv5089934mobile element insertion1nstd203human GRCh38 chr3: 152,263,248-152,263,262 , GRCh37.p13 chr3: 151,981,037-151,981,051 MBNL1, MBNL1-AS1
    nsv5033132inversion1nstd200human GRCh38 chr3: 147,205,794-180,217,342 , GRCh37.p13 chr3: 146,923,581-179,935,130 , LOC105374154, 433 more genes
    nsv4912390copy number variation1nstd200human GRCh38 chr3: 151,409,405-152,510,511 , GRCh37.p13 chr3: 151,127,193-152,228,300 , IGSF10, 17 more genes
    nsv4728455copy number variation1nstd102humanUncertain significance GRCh37 chr3: 151,702,938-152,648,714 , GRCh38.p12 chr3: 151,985,149-152,930,925 ATP5MGP5, TMEM14EP, 6 more genes
    nsv4684209copy number variation1nstd102humanPathogenic GRCh37 chr3: 138,145,289-162,275,610 , GRCh38.p12 chr3: 138,426,447-162,557,822 MTAPP1, PLS1, 339 more genes
    nsv4674301copy number variation1nstd102humanPathogenic GRCh37 chr3: 149,404,255-152,786,331 , GRCh38.p12 chr3: 149,686,468-153,068,542 EIF3JP2, IGSF10, 63 more genes
    nsv4587621copy number variation1nstd183human GRCh37 chr3: 151,897,062-152,174,158 , GRCh38.p12 chr3: 152,179,273-152,456,369 , MBNL1, 3 more genes
    nsv4585357copy number variation1nstd183human GRCh37 chr3: 151,908,402-152,049,366 , GRCh38.p12 chr3: 152,190,613-152,331,577 , MBNL1-AS1, 2 more genes
    nsv4468822mobile element insertion1nstd166human GRCh37.p13 chr3: 151,985,930-151,985,930 , GRCh38.p12 chr3: 152,268,141-152,268,141 MBNL1-AS1, MBNL1
    nsv4433911copy number variation1nstd172human GRCh37.p13 chr3: 151,958,001-152,043,000 , GRCh38.p12 chr3: 152,240,212-152,325,211 , MBNL1, 1 more genes
    nsv4387977copy number variation1nstd173human GRCh37 chr3: 151,924,042-152,070,136 , GRCh38.p12 chr3: 152,206,253-152,352,347 , TMEM14EP, 2 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