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 300

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7098813copy number variation1nstd102humanPathogenic GRCh37 chr12: 176,047-34,179,852 , GRCh38.p12 chr12: 66,881-34,026,917 TDGP1, RPS4XP14, 680 more genes
    nsv7094047copy number variation1nstd102humanUncertain significance GRCh37 chr12: 4,368,352-9,027,607 , GRCh38.p12 chr12: 4,259,186-8,875,011 ACRBP, OR7E148P, 165 more genes
    nsv7077542inversion1nstd229human GRCh38 chr12: 7,565,102-9,354,075 , GRCh37.p13 chr12: 7,717,698-9,506,671 ALG1L10P, RPL15P17, 69 more genes
    nsv7074628inversion1nstd229human GRCh38 chr12: 5,173,229-8,663,348 , GRCh37.p13 chr12: 5,282,395-8,815,944 P3H3, LOC105369621, 141 more genes
    nsv7072221inversion1nstd229human GRCh38 chr12: 4,055,290-11,695,188 , GRCh37.p13 chr12: 4,164,456-11,848,122 RN7SL69P, KLRA1P, 285 more genes
    nsv7068010inversion1nstd229human GRCh38 chr12: 7,025,778-10,225,656 , GRCh37.p13 chr12: 7,178,850-10,378,255 GOT2P3, CLEC2B, 123 more genes
    nsv7064008inversion1nstd229human GRCh38 chr12: 6,716,253-10,225,825 , GRCh37.p13 chr12: 6,825,419-10,378,424 PTMAP4, COPS7A, 153 more genes
    nsv6937927copy number variation1nstd229human GRCh38 chr12: 7,720,289-7,838,364 , GRCh37.p13 chr12: 7,872,885-7,990,960 CLEC4C, NANOG, 2 more genes
    nsv6931262copy number variation1nstd229human GRCh38 chr12: 7,782,698-7,944,328 , GRCh37.p13 chr12: 7,935,294-8,096,924 SLC2A3, SLC2A14, 4 more genes
    nsv6920730copy number variation1nstd229human GRCh38 chr12: 7,768,101-7,791,400 , GRCh37.p13 chr12: 7,920,697-7,943,996 NANOG, NANOGNB
    nsv6637376copy number variation1nstd102humanPathogenic GRCh37 chr12: 173,787-8,320,544 , GRCh38.p12 chr12: 64,621-8,167,948 GCSHP4, RNU7-1, 220 more genes
    nsv6634782copy number variation1nstd227human GRCh38.p12 chr12: 7,782,498-7,969,996 , GRCh37 chr12: 7,935,094-8,122,592 SLC2A3, NANOG, 4 more genes
    nsv6621877copy number variation1nstd224human GRCh37 chr12: 7,832,447-8,374,746 , GRCh38.p12 chr12: 7,679,851-8,222,150 GDF3, NECAP1, 21 more genes
    nsv6621743copy number variation1nstd224human GRCh37 chr12: 7,945,559-8,123,306 , GRCh38.p12 chr12: 7,792,963-7,970,710 SLC2A3, NANOG, 4 more genes
    nsv6585629inversion1nstd223human GRCh38 chr12: 7,791,994-7,792,461 , GRCh37.p13 chr12: 7,944,590-7,945,057 NANOG
    nsv6473551copy number variation1nstd223human GRCh38 chr12: 7,770,716-7,793,845 , GRCh37.p13 chr12: 7,923,312-7,946,441 NANOG, NANOGNB
    nsv6473414copy number variation1nstd223human GRCh38 chr12: 7,798,959-7,905,888 , GRCh37.p13 chr12: 7,951,555-8,058,484 SLC2A14, NANOGP1, 3 more genes
    nsv6472073copy number variation1nstd223human GRCh38 chr12: 7,768,134-7,791,427 , GRCh37.p13 chr12: 7,920,730-7,944,023 NANOGNB, NANOG
    nsv6467885copy number variation1nstd223human GRCh38 chr12: 7,763,859-7,870,109 , GRCh37.p13 chr12: 7,916,455-8,022,705 NANOGNB, SLC2A14, 3 more genes
    nsv6462423copy number variation1nstd223human GRCh38 chr12: 7,674,221-7,829,881 , GRCh37.p13 chr12: 7,826,817-7,982,477 GDF3, SLC2A14, 4 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