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 103

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    nsv5973212inversion1nstd209human GRCh38 chr3: 121,858,185-122,522,926 , GRCh37.p13 chr3: 121,577,032-122,241,773 CASR, CD86, 12 more genes
    nsv5618923insertion1nstd207human GRCh38 chr3: 122,414,100-122,414,100 , GRCh37.p13 chr3: 122,132,947-122,132,947 WDR5B
    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
    nsv4919856copy number variation1nstd200human GRCh38 chr3: 122,415,246-122,416,922 , GRCh37.p13 chr3: 122,134,093-122,135,769 WDR5B-DT, WDR5B
    nsv4806982copy number variation1nstd200human GRCh37 chr3: 122,134,093-122,135,769 , GRCh38.p12 chr3: 122,415,246-122,416,922 WDR5B-DT, WDR5B
    nsv4794327copy number variation1nstd200human GRCh37 chr3: 122,128,252-122,128,800 , GRCh38.p12 chr3: 122,409,405-122,409,953 FAM162A, WDR5B
    nsv4555288insertion1nstd166human GRCh37.p13 chr3: 122,132,947-122,132,947 , GRCh38.p12 chr3: 122,414,100-122,414,100 WDR5B
    nsv4552608insertion1nstd166human GRCh37.p13 chr3: 122,132,903-122,132,903 , GRCh38.p12 chr3: 122,414,056-122,414,056 WDR5B
    nsv4548079insertion1nstd166human GRCh37.p13 chr3: 122,132,950-122,132,950 , GRCh38.p12 chr3: 122,414,103-122,414,103 WDR5B
    nsv4453697copy number variation1nstd102humanUncertain significance GRCh37 chr3: 121,384,741-123,672,180 , GRCh38.p12 chr3: 121,665,894-123,953,333 LOC101927010, IQCB1, 35 more genes
    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
    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