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 243

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7095852copy number variation1nstd102humanUncertain significance GRCh37 chr2: 113,875,596-113,890,448 , GRCh38.p12 chr2: 113,118,019-113,132,871 IL1RN
    nsv7044064inversion1nstd229human GRCh38 chr2: 112,019,946-120,004,832 , GRCh37.p13 chr2: 112,777,523-120,762,408 LOC105373563, IL1A, 112 more genes
    nsv7042586inversion1nstd229human GRCh38 chr2: 111,572,275-118,829,502 , GRCh37.p13 chr2: 112,329,852-119,587,078 LOC105373579, NT5DC4, 103 more genes
    nsv7039561inversion1nstd229human GRCh38 chr2: 112,945,161-113,099,965 , GRCh37.p13 chr2: 113,702,738-113,857,542 IL36G, POLR2DP1, 7 more genes
    nsv6696371copy number variation1nstd229human GRCh38 chr2: 113,114,305-113,116,877 , GRCh37.p13 chr2: 113,871,882-113,874,454 IL1RN
    nsv6695149copy number variation1nstd229human GRCh38 chr2: 113,089,438-113,101,324 , GRCh37.p13 chr2: 113,847,015-113,858,901 IL1RN
    nsv6692839copy number variation1nstd229human GRCh38 chr2: 113,090,343-113,100,132 , GRCh37.p13 chr2: 113,847,920-113,857,709 IL1RN
    nsv6690747copy number variation1nstd229human GRCh38 chr2: 112,960,556-113,135,779 , GRCh37.p13 chr2: 113,718,133-113,893,356 IL36G, POLR2DP1, 7 more genes
    nsv6679673copy number variation1nstd229human GRCh38 chr2: 113,114,986-113,115,209 , GRCh37.p13 chr2: 113,872,563-113,872,786 IL1RN
    nsv6679384copy number variation1nstd229human GRCh38 chr2: 113,064,901-113,421,800 , GRCh37.p13 chr2: 113,822,478-114,179,377 LOC107985936, PAX8-AS1, 8 more genes
    nsv6347631copy number variation1nstd223human GRCh38 chr2: 113,100,001-113,102,100 , GRCh37.p13 chr2: 113,857,578-113,859,677 IL1RN
    nsv6344150copy number variation1nstd223human GRCh38 chr2: 113,010,465-113,106,661 , GRCh37.p13 chr2: 113,768,042-113,864,238 IL1RN, IL36RN, 4 more genes
    nsv6343530copy number variation1nstd223human GRCh38 chr2: 112,960,556-113,135,775 , GRCh37.p13 chr2: 113,718,133-113,893,352 IL1RN, IL36RN, 7 more genes
    nsv6337104copy number variation1nstd223human GRCh38 chr2: 113,064,901-113,421,800 , GRCh37.p13 chr2: 113,822,478-114,179,377 LINC02966, IL1RN, 8 more genes
    nsv6315390copy number variation1nstd102humanPathogenic GRCh37 chr2: 1-243,199,373 , GRCh38.p12 chr2: 10,001-242,157,305 LOC112268439, RNA5SP116, 3737 more genes
    nsv6314748copy number variation1nstd102humanPathogenic GRCh37 chr2: 112,475,655-145,691,999 , GRCh38.p12 chr2: 111,718,078-144,934,432 MED15P9, TMEM37, 474 more genes
    nsv6314726copy number variation1nstd102humanLikely pathogenic GRCh37 chr2: 40,607,042-146,902,764 , GRCh38.p12 chr2: 40,379,902-146,145,196 ACTG2, ACYP2, 1713 more genes
    nsv6313770copy number variation1nstd102humanPathogenic GRCh37 chr2: 113,188,197-128,144,700 , GRCh38.p12 chr2: 112,430,620-127,387,124 LOC105373575, RPS20P11, 174 more genes
    nsv6311288copy number variation2nstd102humanPathogenic GRCh37 chr2: 113,817,016-113,890,448 , GRCh38.p12 chr2: 113,059,439-113,132,871 IL1F10, RNU6-1180P, 2 more genes
    nsv6291353copy number variation1nstd102humanPathogenic GRCh37 chr2: 111,484,468-146,333,604 , GRCh38.p12 chr2: 110,726,891-145,576,036 LINC01120, LOC105373585, 490 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