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 240

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7065187inversion1nstd229human GRCh38 chr18: 24,331,965-24,490,008 , GRCh37.p13 chr18: 21,911,929-22,069,972 HRH4, OSBPL1A, 1 more genes
    nsv7062236inversion1nstd229human GRCh38 chr18: 24,448,556-24,448,632 , GRCh37.p13 chr18: 22,028,520-22,028,596 IMPACT
    nsv7013482copy number variation1nstd229human GRCh38 chr18: 24,452,601-24,492,800 , GRCh37.p13 chr18: 22,032,565-22,072,764 IMPACT, HRH4
    nsv7010764copy number variation1nstd229human GRCh38 chr18: 24,425,301-24,444,100 , GRCh37.p13 chr18: 22,005,265-22,024,064 IMPACT
    nsv7002801copy number variation1nstd229human GRCh38 chr18: 24,425,386-24,441,267 , GRCh37.p13 chr18: 22,005,350-22,021,231 IMPACT
    nsv7001485copy number variation1nstd229human GRCh38 chr18: 23,020,759-30,428,209 , GRCh37.p13 chr18: 20,600,722-28,008,175 RN7SL97P, RIOK3, 76 more genes
    nsv7000010copy number variation1nstd229human GRCh38 chr18: 24,440,152-24,440,178 , GRCh37.p13 chr18: 22,020,116-22,020,142 IMPACT
    nsv6624375copy number variation1nstd224human GRCh37 chr18: 22,012,716-22,348,248 , GRCh38.p12 chr18: 24,432,752-24,768,284 LOC105372028, HRH4, 8 more genes
    nsv6583312inversion1nstd223human GRCh38 chr18: 24,434,823-24,434,980 , GRCh37.p13 chr18: 22,014,787-22,014,944 IMPACT
    nsv6534138copy number variation1nstd223human GRCh38 chr18: 24,447,399-24,448,057 , GRCh37.p13 chr18: 22,027,363-22,028,021 IMPACT
    nsv6521817copy number variation1nstd223human GRCh38 chr18: 24,429,989-24,431,542 , GRCh37.p13 chr18: 22,009,953-22,011,506 IMPACT
    nsv6315530copy number variation1nstd102humanPathogenic GRCh37 chr18: 1-78,077,248 , GRCh38.p12 chr18: 10,001-80,259,271 LOC105372145, LOC105372016, 947 more genes
    nsv6314722copy number variation1nstd102humanPathogenic GRCh37 chr18: 1,262,334-53,254,751 , GRCh38.p12 chr18: 1,262,333-55,587,520 LOC107985176, ZNF521, 632 more genes
    nsv6291786copy number variation1nstd102humanPathogenic GRCh37 chr18: 136,226-25,252,276 , GRCh38.p12 chr18: 136,226-27,672,312 LOC107985122, LOC100130487, 375 more genes
    nsv6291540copy number variation1nstd102humanUncertain significance GRCh37 chr18: 18,611,942-26,843,691 , GRCh38.p12 chr18: 21,031,981-29,263,726 MIR133A1HG, LOC105372040, 111 more genes
    nsv6259252mobile element insertion1nstd215human GRCh38 chr18: 24,435,887-24,435,887 , GRCh37.p13 chr18: 22,015,851-22,015,851 IMPACT
    nsv6133380copy number variation1nstd213human GRCh37 chr18: 21,980,000-24,910,001 , GRCh38.p12 chr18: 24,400,036-27,330,037 NPM1P2, SS18, 39 more genes
    nsv6114957mobile element insertion1nstd186human GRCh37 chr18: 22,015,835-22,015,835 , GRCh38.p12 chr18: 24,435,871-24,435,871 IMPACT
    nsv6105900insertion1nstd212human GRCh38 chr18: 24,435,871-24,435,871 , GRCh37.p13 chr18: 22,015,835-22,015,835 IMPACT
    nsv5973171insertion1nstd209human GRCh38 chr18: 24,435,871-24,435,871 , GRCh37.p13 chr18: 22,015,835-22,015,835 IMPACT
    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