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Items: 1 to 20 of 547

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137099copy number variation1nstd102humanPathogenic GRCh37 chr12: 11,463,270-14,019,142 , GRCh38.p12 chr12: 11,310,336-13,866,208 HTR7P1, RPL37AP9, 55 more genes
    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
    nsv7066406inversion1nstd229human GRCh38 chr12: 10,925,081-12,847,121 , GRCh37.p13 chr12: 11,077,680-13,000,055 RPL19P17, TAS2R64P, 56 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
    nsv7064011inversion1nstd229human GRCh38 chr12: 11,255,910-17,864,916 , GRCh37.p13 chr12: 11,408,826-18,017,850 MGP, MIR3974, 108 more genes
    nsv6937644copy number variation1nstd229human GRCh38 chr12: 11,352,001-11,394,000 , GRCh37.p13 chr12: 11,504,935-11,546,934 PRB1, PRB2
    nsv6934551copy number variation1nstd229human GRCh38 chr12: 11,352,301-11,395,700 , GRCh37.p13 chr12: 11,505,235-11,548,634 PRB1, PRB2
    nsv6934504copy number variation1nstd229human GRCh38 chr12: 11,346,201-11,392,700 , GRCh37.p13 chr12: 11,499,135-11,545,634 PRB2, PRB1
    nsv6934316copy number variation1nstd229human GRCh38 chr12: 11,352,101-11,393,000 , GRCh37.p13 chr12: 11,505,035-11,545,934 PRB1, PRB2
    nsv6934103copy number variation1nstd229human GRCh38 chr12: 11,352,201-11,402,900 , GRCh37.p13 chr12: 11,505,135-11,555,834 PRB2, PRB1
    nsv6929994copy number variation1nstd229human GRCh38 chr12: 11,351,401-11,393,900 , GRCh37.p13 chr12: 11,504,335-11,546,834 PRB1, PRB2
    nsv6928904copy number variation1nstd229human GRCh38 chr12: 11,350,601-11,396,000 , GRCh37.p13 chr12: 11,503,535-11,548,934 PRB1, PRB2
    nsv6924022copy number variation1nstd229human GRCh38 chr12: 11,351,901-11,396,200 , GRCh37.p13 chr12: 11,504,835-11,549,134 PRB1, PRB2
    nsv6922376copy number variation1nstd229human GRCh38 chr12: 11,351,601-11,406,400 , GRCh37.p13 chr12: 11,504,535-11,559,334 PRB2, PRB1
    nsv6918561copy number variation1nstd229human GRCh38 chr12: 11,327,123-11,383,581 , GRCh37.p13 chr12: 11,480,057-11,536,515 PRB1
    nsv6634456copy number variation1nstd102humanPathogenic GRCh37 chr12: 10,853,887-24,103,810 , GRCh38.p12 chr12: 10,701,288-23,950,876 TAS2R15P, LOC105369673, 209 more genes
    nsv6621502copy number variation1nstd224human GRCh37 chr12: 11,495,064-11,585,360 , GRCh38.p12 chr12: 11,342,130-11,432,426 PRB1, LOC440084, 1 more genes
    nsv6621501copy number variation1nstd224human GRCh37 chr12: 11,463,322-11,547,532 , GRCh38.p12 chr12: 11,310,388-11,394,598 , GRCh38.p12 chr12|NT_187658.1: 505,351-572,349 PRB2, PRB1, 1 more genes
    nsv6621311copy number variation1nstd224human GRCh37 chr12: 11,495,064-11,600,552 , GRCh38.p12 chr12: 11,342,130-11,447,618 LOC440084, PRB2, 1 more genes
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