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 149

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148084copy number variation1nstd102humanPathogenic GRCh37 chr3: 3,669,542-9,937,745 , GRCh38.p12 chr3: 3,627,858-9,896,061 LOC105376943, GRM7-AS2, 71 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
    nsv6717492copy number variation1nstd229human GRCh38 chr3: 9,728,301-10,020,500 , GRCh37.p13 chr3: 9,769,985-10,062,184 CPNE9, OGG1, 22 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
    nsv6714485copy number variation1nstd229human GRCh38 chr3: 9,761,673-9,761,849 , GRCh37.p13 chr3: 9,803,357-9,803,533 CAMK1, OGG1
    nsv6711500copy number variation1nstd229human GRCh38 chr3: 9,761,512-9,764,835 , GRCh37.p13 chr3: 9,803,196-9,806,519 CAMK1, OGG1
    nsv6708056copy number variation1nstd229human GRCh38 chr3: 9,670,964-9,796,009 , GRCh37.p13 chr3: 9,712,648-9,837,693 OGG1, BRPF1, 6 more genes
    nsv6707180copy number variation1nstd229human GRCh38 chr3: 9,756,144-9,760,025 , GRCh37.p13 chr3: 9,797,828-9,801,709 OGG1, CAMK1
    nsv6702711copy number variation1nstd229human GRCh38 chr3: 9,506,401-9,914,700 , GRCh37.p13 chr3: 9,548,085-9,956,384 CAMK1, MARK2P1, 15 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
    nsv6636296copy number variation1nstd102humanPathogenic GRCh37 chr3: 61,892-9,899,605 , GRCh38.p12 chr3: 20,214-9,857,921 GRM7-AS1, LOC105376938, 101 more genes
    nsv6636289copy number variation1nstd102humanUncertain significance GRCh37 chr3: 9,754,612-10,295,828 , GRCh38.p12 chr3: 9,712,928-10,254,144 FANCD2P1, RNU6-882P, 30 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
    nsv6362532copy number variation1nstd223human GRCh38 chr3: 9,495,638-9,874,055 , GRCh37.p13 chr3: 9,537,322-9,915,739 LOC105376949, CPNE9, 13 more genes
    nsv6313626copy number variation1nstd102humanUncertain significance GRCh37 chr3: 9,754,611-10,295,828 , GRCh38.p12 chr3: 9,712,927-10,254,144 MARK2P1, CIDEC, 30 more genes
    nsv6313525copy number variation1nstd102humanPathogenic GRCh37 chr3: 61,891-9,797,094 , GRCh38.p12 chr3: 20,213-9,755,410 EGOT, LOC107986040, 95 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
    nsv6311805copy number variation1nstd102humanUncertain significance GRCh37 chr3: 8,775,563-9,986,075 , GRCh38.p12 chr3: 8,733,877-9,944,391 SRGAP3, MARK2P1, 33 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