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 247

    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
    nsv7077542inversion1nstd229human GRCh38 chr12: 7,565,102-9,354,075 , GRCh37.p13 chr12: 7,717,698-9,506,671 ALG1L10P, RPL15P17, 69 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
    nsv7072108inversion1nstd229human GRCh38 chr12: 9,111,990-9,112,090 , GRCh37.p13 chr12: 9,264,586-9,264,686 KLRG1, A2M
    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
    nsv7059773inversion1nstd229human GRCh38 chr12: 8,963,554-9,585,969 , GRCh37.p13 chr12: 9,116,150-9,738,565 DDX12P, LOC105369647, 20 more genes
    nsv6935262copy number variation1nstd229human GRCh38 chr12: 9,069,701-9,079,900 , GRCh37.p13 chr12: 9,222,297-9,232,496 KLRG1, A2M
    nsv6931578copy number variation1nstd229human GRCh38 chr12: 9,096,177-9,096,423 , GRCh37.p13 chr12: 9,248,773-9,249,019 KLRG1, A2M
    nsv6930898copy number variation1nstd229human GRCh38 chr12: 9,074,786-9,076,755 , GRCh37.p13 chr12: 9,227,382-9,229,351 A2M, KLRG1
    nsv6926772copy number variation1nstd229human GRCh38 chr12: 9,084,418-9,098,728 , GRCh37.p13 chr12: 9,237,014-9,251,324 A2M, KLRG1
    nsv6637627copy number variation1nstd102humanUncertain significance GRCh37 chr12: 8,781,515-9,605,163 , GRCh38.p12 chr12: 8,628,919-9,452,567 A2MP1, LOC101928030, 26 more genes
    nsv6466072copy number variation1nstd223human GRCh38 chr12: 9,093,601-9,098,900 , GRCh37.p13 chr12: 9,246,197-9,251,496 A2M, KLRG1
    nsv6463326copy number variation1nstd223human GRCh38 chr12: 9,086,295-9,086,757 , GRCh37.p13 chr12: 9,238,891-9,239,353 KLRG1, A2M
    nsv6461865copy number variation1nstd223human GRCh38 chr12: 9,084,601-9,085,900 , GRCh37.p13 chr12: 9,237,197-9,238,496 A2M, KLRG1
    nsv6461241copy number variation1nstd223human GRCh38 chr12: 9,103,431-9,103,966 , GRCh37.p13 chr12: 9,256,027-9,256,562 A2M, KLRG1
    nsv6461183copy number variation1nstd223human GRCh38 chr12: 9,114,301-9,115,000 , GRCh37.p13 chr12: 9,266,897-9,267,596 A2M, KLRG1
    nsv6459518copy number variation1nstd223human GRCh38 chr12: 9,112,275-9,112,924 , GRCh37.p13 chr12: 9,264,871-9,265,520 KLRG1, A2M
    nsv6240645mobile element insertion1nstd215human GRCh38 chr12: 9,114,660-9,114,660 , GRCh37.p13 chr12: 9,267,256-9,267,256 KLRG1, A2M
    nsv6132720copy number variation1nstd213human GRCh37 chr12: 9,040,000-17,930,001 , GRCh38.p12 chr12: 8,887,404-17,777,067 A2M, A2MP1, 215 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