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 211

    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
    nsv7074628inversion1nstd229human GRCh38 chr12: 5,173,229-8,663,348 , GRCh37.p13 chr12: 5,282,395-8,815,944 P3H3, LOC105369621, 141 more genes
    nsv7074109inversion1nstd229human GRCh38 chr12: 6,892,196-6,930,768 , GRCh37.p13 chr12|NW_003871083.2: 93,780-132,351 , GRCh37.p13 chr12: 7,001,360-7,039,931 ENO2, LRRC23, 1 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
    nsv7064008inversion1nstd229human GRCh38 chr12: 6,716,253-10,225,825 , GRCh37.p13 chr12: 6,825,419-10,378,424 PTMAP4, COPS7A, 153 more genes
    nsv6932613copy number variation1nstd229human GRCh38 chr12: 6,918,162-6,919,563 , GRCh37.p13 chr12: 7,027,326-7,028,727 , GRCh37.p13 chr12|NW_003871083.2: 119,746-121,147 ENO2
    nsv6926955copy number variation1nstd229human GRCh38 chr12: 6,920,498-6,924,861 , GRCh37.p13 chr12: 7,029,661-7,034,024 , GRCh37.p13 chr12|NW_003871083.2: 122,081-126,444 ENO2, ATN1
    nsv6926326copy number variation1nstd229human GRCh38 chr12: 6,904,787-6,915,750 , GRCh37.p13 chr12|NW_003871083.2: 106,371-117,334 , GRCh37.p13 chr12: 7,013,951-7,024,914 ENO2, LRRC23
    nsv6922064copy number variation1nstd229human GRCh38 chr12: 6,908,322-6,912,600 , GRCh37.p13 chr12|NW_003871083.2: 109,906-114,184 , GRCh37.p13 chr12: 7,017,486-7,021,764 LRRC23, ENO2
    nsv6637376copy number variation1nstd102humanPathogenic GRCh37 chr12: 173,787-8,320,544 , GRCh38.p12 chr12: 64,621-8,167,948 GCSHP4, RNU7-1, 220 more genes
    nsv6475282copy number variation1nstd223human GRCh38 chr12: 6,874,498-6,920,071 , GRCh37.p13 chr12: 6,983,662-7,028,982 , GRCh37.p13 chr12|NW_003871083.2: 76,082-121,654 LOC105369632, LRRC23, 3 more genes
    nsv6472373copy number variation1nstd223human GRCh38 chr12: 6,012,501-7,083,600 , GRCh37.p13 chr12: 6,121,667-7,189,876 GPR162, CD27, 71 more genes
    nsv6472196copy number variation1nstd223human GRCh38 chr12: 6,013,501-7,083,700 , GRCh37.p13 chr12: 6,122,667-7,189,876 SCARNA10, ATP5MFP5, 71 more genes
    nsv6314186copy number variation1nstd102humanUncertain significance GRCh37 chr12: 6,872,634-7,244,086 , GRCh38.p12 chr12: 6,763,468-7,091,490 DSTNP2, ENO2, 30 more genes
    nsv6313934copy number variation1nstd102humanUncertain significance GRCh37 chr12: 6,530,146-7,376,398 , GRCh38.p12 chr12: 6,420,980-7,223,802 VAMP1, CD27-AS1, 60 more genes
    nsv6309483copy number variation1nstd102humanUncertain significance GRCh37 chr12: 6,438,478-8,756,953 , GRCh38.p12 chr12: 6,329,312-8,604,357 ENPP7P5, GPR162, 122 more genes
    nsv6309328copy number variation1nstd102humanUncertain significance GRCh37 chr12: 6,978,008-9,010,204 , GRCh38.p12 chr12: 6,868,844-8,857,608 LOC101927966, SNRPCP7, 87 more genes
    nsv6309326copy number variation2nstd102humanUncertain significance GRCh37 chr12: 6,438,478-8,248,686 , GRCh38.p12 chr12: 6,329,312-8,096,090 NANOGNB, SCNN1A, 94 more genes
    nsv6290254copy number variation1nstd102humanPathogenic GRCh37 chr12: 146,240-8,330,229 , GRCh38.p12 chr12: 45,740-8,177,633 CLEC4A, FBXL14, 220 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