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 344

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7096705copy number variation1nstd102humanUncertain significance GRCh37 chr3: 183,368,145-184,094,097 , GRCh38.p12 chr3: 183,650,357-184,376,309 VWA5B2, MIR1224, 35 more genes
    nsv7096553copy number variation2nstd102humanPathogenic, Uncertain significance GRCh37 chr3: 182,733,226-184,094,097 , GRCh38.p12 chr3: 183,015,438-184,376,309 DVL3, LOC105374247, 51 more genes
    nsv7053971inversion1nstd229human GRCh38 chr3: 183,609,736-184,280,209 , GRCh37.p13 chr3: 183,327,524-183,997,997 HTR3C2P, YEATS2-AS1, 31 more genes
    nsv6735553copy number variation1nstd229human GRCh38 chr3: 183,683,501-183,694,000 , GRCh37.p13 chr3: 183,401,289-183,411,788 KLHL24
    nsv6732157copy number variation1nstd229human GRCh38 chr3: 183,634,501-183,636,800 , GRCh37.p13 chr3: 183,352,289-183,354,588 KLHL24, LOC107986162
    nsv6731350copy number variation1nstd229human GRCh38 chr3: 183,681,897-183,681,926 , GRCh37.p13 chr3: 183,399,685-183,399,714 KLHL24
    nsv6731049copy number variation1nstd229human GRCh38 chr3: 183,641,701-183,644,700 , GRCh37.p13 chr3: 183,359,489-183,362,488 KLHL24
    nsv6723338copy number variation1nstd229human GRCh38 chr3: 183,439,501-183,733,400 , GRCh37.p13 chr3: 183,157,289-183,451,188 LOC105374248, YEATS2, 8 more genes
    nsv6722991copy number variation1nstd229human GRCh38 chr3: 183,636,716-183,640,218 , GRCh37.p13 chr3: 183,354,504-183,358,006 KLHL24, LOC107986162
    nsv6719234copy number variation1nstd229human GRCh38 chr3: 183,670,001-183,690,500 , GRCh37.p13 chr3: 183,387,789-183,408,288 KLHL24
    nsv6634384copy number variation1nstd102humanPathogenic GRCh37 chr3: 181,062,175-185,474,509 , GRCh38.p12 chr3: 181,344,387-185,756,721 PRICKLE1P1, KLHL24, 99 more genes
    nsv6634371copy number variation1nstd102humanLikely pathogenic GRCh37 chr3: 171,549,421-198,022,430 , GRCh38.p12 chr3: 171,831,631-198,235,559 ACTL6A, AHSG, 466 more genes
    nsv6573478inversion1nstd223human GRCh38 chr3: 183,640,611-183,641,210 , GRCh37.p13 chr3: 183,358,399-183,358,998 KLHL24
    nsv6565814inversion1nstd223human GRCh38 chr3: 183,647,032-183,647,224 , GRCh37.p13 chr3: 183,364,820-183,365,012 KLHL24
    nsv6560083inversion1nstd223human GRCh38 chr3: 183,639,510-183,640,594 , GRCh37.p13 chr3: 183,357,298-183,358,382 KLHL24
    nsv6375075copy number variation1nstd223human GRCh38 chr3: 183,676,701-183,677,500 , GRCh37.p13 chr3: 183,394,489-183,395,288 KLHL24
    nsv6370950copy number variation1nstd223human GRCh38 chr3: 183,680,805-183,681,430 , GRCh37.p13 chr3: 183,398,593-183,399,218 KLHL24
    nsv6368749copy number variation1nstd223human GRCh38 chr3: 183,665,696-183,669,250 , GRCh37.p13 chr3: 183,383,484-183,387,038 KLHL24
    nsv6362224copy number variation1nstd223human GRCh38 chr3: 183,678,278-183,678,646 , GRCh37.p13 chr3: 183,396,066-183,396,434 KLHL24
    nsv6313539copy number variation1nstd102humanPathogenic GRCh37 chr3: 182,189,525-187,212,935 , GRCh38.p12 chr3: 182,471,737-187,495,147 ALG3, MIR4448, 133 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