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 140

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5447805copy number variation1nstd206human GRCh38 chr3: 158,831,574-159,228,000 , GRCh37.p13 chr3: 158,549,363-158,945,789 GPR79, IQCJ, 2 more genes
    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
    nsv5033132inversion1nstd200human GRCh38 chr3: 147,205,794-180,217,342 , GRCh37.p13 chr3: 146,923,581-179,935,130 , LOC105374154, 433 more genes
    nsv4920241copy number variation1nstd200human GRCh38 chr3: 158,754,716-158,907,395 , GRCh37.p13 chr3: 158,472,505-158,625,184 GPR79, MFSD1, 3 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
    nsv4684148copy number variation1nstd102humanUncertain significance GRCh37 chr3: 156,812,581-160,154,747 , GRCh38.p12 chr3: 157,094,792-160,436,959 RSRC1, SMC4, 48 more genes
    nsv4680693copy number variation1nstd189human GRCh37.p13 chr3: 158,341,623-159,202,634 , GRCh38.p12 chr3: 158,623,834-159,484,845 , RARRES1, 12 more genes
    nsv4585010copy number variation1nstd183human GRCh37 chr3: 158,070,463-158,780,214 , GRCh38.p12 chr3: 158,352,674-159,062,425 , MLF1, 13 more genes
    nsv4450004copy number variation1nstd102humanUncertain significance GRCh37 chr3: 158,149,940-158,802,473 , GRCh38.p12 chr3: 158,432,151-159,084,684 GPR79, RSRC1, 14 more genes
    nsv4409492copy number variation1nstd174human GRCh37 chr3: 158,549,548-158,811,068 , GRCh38.p12 chr3: 158,831,759-159,093,279 IQCJ-SCHIP1, LOC105374181, 2 more genes
    nsv4404621copy number variation1nstd174human GRCh37 chr3: 158,475,824-158,646,449 , GRCh38.p12 chr3: 158,758,035-158,928,660 GPR79, MFSD1, 3 more genes
    nsv4386351copy number variation1nstd173human GRCh37 chr3: 158,541,198-158,719,366 , GRCh38.p12 chr3: 158,823,409-159,001,577 LOC105374181, MFSD1, 1 more genes
    nsv4372862copy number variation2nstd173human GRCh37 chr3: 158,377,404-158,776,705 , GRCh38.p12 chr3: 158,659,615-159,058,916 , RARRES1, 7 more genes
    nsv4327395inversion1nstd166human GRCh37.p13 chr3: 126,265,569-194,265,571 , GRCh38.p12 chr3: 126,546,726-194,544,842 , ACTG1P1, 1039 more genes
    nsv4327115inversion1nstd166human GRCh37.p13 chr3: 131,882,701-162,233,318 , GRCh38.p12 chr3: 132,163,857-162,515,530 , ATP1B3, 446 more genes
    nsv3924842copy number variation1nstd102humanconflicting data from submitters NCBI36 chr3: 159,908,348-160,147,919 , GRCh37 chr3: 158,425,654-158,665,225 , GRCh38 chr3: 158,707,865-158,947,436 GPR79, MFSD1, 4 more genes
    nsv3924414copy number variation1nstd102humanUncertain significance GRCh38 chr3: 158,614,801-159,429,760 , GRCh37 chr3: 158,332,590-159,147,549 , NCBI36 chr3: 159,815,284-160,630,243 GPR79, MFSD1, 11 more genes
    nsv3922763copy number variation1nstd102humanUncertain significance NCBI36 chr3: 159,852,707-160,236,939 , GRCh37 chr3: 158,370,013-158,754,245 , GRCh38 chr3: 158,652,224-159,036,456 LXN, RPL35AP9, 6 more genes
    nsv3919833copy number variation1nstd102humanPathogenic GRCh38 chr3: 158,141,556-172,788,324 , NCBI36 chr3: 159,342,039-173,988,808 , GRCh37 chr3: 157,859,345-172,506,114 NMD3, TRV-AAC1-1, 173 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
    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