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    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
    nsv7072221inversion1nstd229human GRCh38 chr12: 4,055,290-11,695,188 , GRCh37.p13 chr12: 4,164,456-11,848,122 RN7SL69P, KLRA1P, 285 more genes
    nsv7064789inversion1nstd229human GRCh38 chr12: 10,249,571-12,880,432 , GRCh37.p13 chr12: 10,402,170-13,033,366 DDX47, TAS2R64P, 89 more genes
    nsv7064629inversion1nstd229human GRCh38 chr12: 10,296,462-11,054,955 , GRCh37.p13 chr12: 10,449,061-11,207,554 TAS2R31, EIF2S3B, 39 more genes
    nsv6933855copy number variation1nstd229human GRCh38 chr12: 10,394,101-10,615,900 , GRCh37.p13 chr12: 10,546,700-10,768,499 LOC105376675, SLC25A39P2, 12 more genes
    nsv6926383copy number variation1nstd229human GRCh38 chr12: 10,011,885-10,447,510 , GRCh37.p13 chr12: 10,164,484-10,600,109 KLRC1, LOC102724020, 20 more genes
    nsv6593007inversion1nstd223human GRCh38 chr12: 10,345,792-10,519,384 , GRCh37.p13 chr12: 10,498,391-10,671,983 KLRC1, KLRC2, 7 more genes
    nsv6473103copy number variation1nstd223human GRCh38 chr12: 10,427,919-10,443,397 , GRCh37.p13 chr12: 10,580,518-10,595,996 KLRC1, KLRC2
    nsv6472839copy number variation1nstd223human GRCh38 chr12: 10,447,801-10,449,700 , GRCh37.p13 chr12: 10,600,400-10,602,299 KLRC1
    nsv6472783copy number variation1nstd223human GRCh38 chr12: 10,423,301-10,449,100 , GRCh37.p13 chr12: 10,575,900-10,601,699 KLRC1, KLRC2
    nsv6470957copy number variation1nstd223human GRCh38 chr12: 10,448,125-10,448,552 , GRCh37.p13 chr12: 10,600,724-10,601,151 KLRC1
    nsv6470172copy number variation1nstd223human GRCh38 chr12: 10,388,401-10,458,200 , GRCh37.p13 chr12: 10,541,000-10,610,799 KLRC1, KLRC2, 5 more genes
    nsv6469828copy number variation1nstd223human GRCh38 chr12: 10,428,901-10,445,500 , GRCh37.p13 chr12: 10,581,500-10,598,099 KLRC2, KLRC1
    nsv6462653copy number variation1nstd223human GRCh38 chr12: 10,429,001-10,452,900 , GRCh37.p13 chr12: 10,581,600-10,605,499 KLRC2, KLRC1
    nsv6305289copy number variation1nstd186human GRCh37 chr12: 10,587,249-10,592,599 , GRCh38.p12 chr12: 10,434,650-10,440,000 KLRC1, KLRC2
    nsv6144138copy number variation1nstd206human GRCh38 chr12: 10,418,650-10,440,650 , GRCh37.p13 chr12: 10,571,249-10,593,249 KLRC1, KLRC2, 1 more genes
    nsv6143465copy number variation1nstd206human GRCh38 chr12: 10,434,650-10,440,000 , GRCh37.p13 chr12: 10,587,249-10,592,599 KLRC2, KLRC1
    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
    nsv6132616copy number variation1nstd213human GRCh37 chr12: 8,100,000-12,900,001 , GRCh38.p12 chr12: 7,947,404-12,747,067 A2M, A2MP1, 178 more genes
    nsv6132445copy number variation1nstd213human GRCh37 chr12: 9,040,000-11,190,001 , GRCh38.p12 chr12: 8,887,404-11,037,402 A2M, A2MP1, 95 more genes
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