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 207

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7052230inversion1nstd229human GRCh38 chr2: 113,516,629-113,603,263 , GRCh37.p13 chr2: 114,274,206-114,360,840 DDX11L2, FAM138B, 4 more genes
    nsv7047201inversion1nstd229human GRCh38 chr2: 113,135,467-114,194,806 , GRCh37.p13 chr2: 113,893,044-114,952,383 SLC35F5, ACRP1, 26 more genes
    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
    nsv6553311inversion1nstd223human GRCh38 chr2: 113,382,126-121,687,299 , GRCh37.p13 chr2: 114,139,703-122,444,875 RPSAP23, CCDC93, 98 more genes
    nsv6552659inversion1nstd223human GRCh38 chr2: 113,602,835-113,603,198 , GRCh37.p13 chr2: 114,360,412-114,360,775 DDX11L2
    nsv6552069inversion1nstd223human GRCh38 chr2: 113,602,703-113,603,235 , GRCh37.p13 chr2: 114,360,280-114,360,812 DDX11L2
    nsv6540096inversion1nstd223human GRCh38 chr2: 113,602,734-113,603,295 , GRCh37.p13 chr2: 114,360,311-114,360,872 DDX11L2
    nsv6344490copy number variation1nstd223human GRCh38 chr2: 113,468,001-113,722,400 , GRCh37.p13 chr2: 114,225,578-114,479,977 ZNG1B, RPL23AP7, 15 more genes
    nsv6337775copy number variation1nstd223human GRCh38 chr2: 113,469,601-113,720,200 , GRCh37.p13 chr2: 114,227,178-114,477,777 FOXD4L1, ZNG1B, 15 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
    nsv6296225copy number variation1nstd186human GRCh37 chr2: 113,990,735-114,562,290 , GRCh38.p12 chr2: 113,233,158-113,804,713 , PAX8-AS1, 22 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
    nsv6291014copy number variation1nstd102humanUncertain significance GRCh37 chr2: 113,609,489-115,817,535 , GRCh38.p12 chr2: 112,851,912-115,059,958 PSD4, PGM5P4, 43 more genes
    nsv6277510insertion1nstd214human GRCh38 chr2: 113,603,732-113,603,732 , GRCh37.p13 chr2: 114,361,309-114,361,309 DDX11L2
    nsv6057654insertion1nstd212human GRCh38 chr2: 113,603,790-113,603,790 , GRCh37.p13 chr2: 114,361,367-114,361,367 DDX11L2
    nsv6049251insertion1nstd212human GRCh38 chr2: 113,602,891-113,602,891 , GRCh37.p13 chr2: 114,360,468-114,360,468 DDX11L2
    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