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 124

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148081copy number variation1nstd102humanPathogenic GRCh37 chr3: 10,167,260-12,533,766 , GRCh38.p12 chr3: 10,125,576-12,492,267 SLC6A1-AS1, LOC101927467, 37 more genes
    nsv7096528copy number variation1nstd102humanPathogenic GRCh37 chr3: 10,094,051-11,078,652 , GRCh38.p12 chr3: 10,052,367-11,036,966 LINC00606, MIR378B, 19 more genes
    nsv7055847inversion1nstd229human GRCh38 chr3: 5,111,802-11,290,661 , GRCh37.p13 chr3: 5,153,487-11,332,347 GHRLOS, LHFPL4, 96 more genes
    nsv7042755inversion1nstd229human GRCh38 chr3: 8,982,205-12,221,239 , GRCh37.p13 chr3: 9,023,889-12,262,739 SYN2, MTCO1P5, 74 more genes
    nsv6715869copy number variation1nstd229human GRCh38 chr3: 9,686,801-10,627,600 , GRCh37.p13 chr3: 9,728,485-10,669,285 FANCD2OS, CRELD1, 40 more genes
    nsv6698744copy number variation1nstd229human GRCh38 chr3: 10,083,301-10,510,500 , GRCh37.p13 chr3: 10,124,985-10,552,184 MIR885, IRAK2, 12 more genes
    nsv6637145copy number variation1nstd102humanPathogenic GRCh37 chr3: 60,931-10,687,964 , GRCh38.p12 chr3: 19,253-10,646,279 RN7SL120P, LOC105376940, 132 more genes
    nsv6637039copy number variation1nstd102humanPathogenic GRCh37 chr3: 10,024,917-11,917,048 , GRCh38.p12 chr3: 9,983,233-11,875,574 ATG7, GHRL, 35 more genes
    nsv6636276copy number variation1nstd102humanPathogenic GRCh37 chr3: 61,892-11,679,509 , GRCh38.p12 chr3: 20,214-11,638,035 RPL23AP39, LOC107986059, 144 more genes
    nsv6540919inversion1nstd223human GRCh38 chr3: 9,115,607-13,898,149 , GRCh37.p13 chr3: 9,157,291-13,939,646 MKRN2OS, RAF1, 106 more genes
    nsv6311883copy number variation1nstd102humanUncertain significance GRCh37 chr3: 7,782,024-11,078,652 , GRCh38.p12 chr3: 7,740,337-11,036,966 CIDECP1, LMCD1, 71 more genes
    nsv6135258copy number variation1nstd213human GRCh37 chr3: 9,900,000-10,780,001 , GRCh38.p12 chr3: 9,858,316-10,738,316 ATP2B2, FANCD2, 29 more genes
    nsv5995049copy number variation1nstd212human GRCh38 chr3: 9,995,584-11,870,473 , GRCh37.p13 chr3: 10,037,268-11,911,947 , VHL, 35 more genes
    nsv5990783copy number variation1nstd212human GRCh38 chr3: 10,050,341-11,870,472 , GRCh37.p13 chr3: 10,092,025-11,911,946 , SLC6A1, 29 more genes
    nsv5904127copy number variation1nstd209human GRCh38 chr3: 9,996,659-11,875,087 , GRCh37.p13 chr3: 10,038,343-11,916,561 , EMC3, 35 more genes
    nsv5901270copy number variation1nstd209human GRCh38 chr3: 10,048,544-11,870,471 , GRCh37.p13 chr3: 10,090,228-11,911,945 , SLC6A11, 29 more genes
    nsv5891525copy number variation1nstd209human GRCh38 chr3: 9,996,478-11,874,953 , GRCh37.p13 chr3: 10,038,162-11,916,427 , TATDN2, 35 more genes
    nsv5037434inversion1nstd200human GRCh38 chr3: 5,031,119-56,902,223 , GRCh37.p13 chr3: 5,072,804-56,936,251 , IRAK2, 925 more genes
    nsv5030280inversion1nstd200human GRCh38 chr3: 3,432,416-77,775,308 , GRCh37.p13 chr3: 3,474,100-77,824,459 , BHLHE40, 1198 more genes
    nsv4888770inversion1nstd200human GRCh37 chr3: 3,474,100-77,824,459 , GRCh38.p12 chr3: 3,432,416-77,775,308 , ATRIP, 1198 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