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Items: 1 to 20 of 199

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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
    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
    nsv6937270copy number variation1nstd229human GRCh38 chr12: 12,321,031-12,327,082 , GRCh37.p13 chr12: 12,473,965-12,480,016 MANSC1
    nsv6933412copy number variation1nstd229human GRCh38 chr12: 12,331,601-12,343,500 , GRCh37.p13 chr12: 12,484,535-12,496,434 MANSC1, RPL23AP66
    nsv6932408copy number variation1nstd229human GRCh38 chr12: 12,346,183-12,346,203 , GRCh37.p13 chr12: 12,499,117-12,499,137 MANSC1
    nsv6929466copy number variation1nstd229human GRCh38 chr12: 12,316,664-12,329,023 , GRCh37.p13 chr12: 12,469,598-12,481,957 MANSC1
    nsv6928462copy number variation1nstd229human GRCh38 chr12: 12,164,118-12,372,992 , GRCh37.p13 chr12: 12,317,052-12,525,926 RNU6-545P, LRP6, 7 more genes
    nsv6923875copy number variation1nstd229human GRCh38 chr12: 12,318,191-12,328,034 , GRCh37.p13 chr12: 12,471,125-12,480,968 MANSC1
    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
    nsv6594538inversion1nstd223human GRCh38 chr12: 12,336,624-12,337,162 , GRCh37.p13 chr12: 12,489,558-12,490,096 RPL23AP66, MANSC1
    nsv6576406inversion1nstd223human GRCh38 chr12: 12,328,440-12,328,862 , GRCh37.p13 chr12: 12,481,374-12,481,796 MANSC1
    nsv6474999copy number variation1nstd223human GRCh38 chr12: 12,348,801-12,352,900 , GRCh37.p13 chr12: 12,501,735-12,505,834 MANSC1
    nsv6470418copy number variation1nstd223human GRCh38 chr12: 12,318,191-12,328,029 , GRCh37.p13 chr12: 12,471,125-12,480,963 MANSC1
    nsv6309465copy number variation2nstd102humanUncertain significance GRCh37 chr12: 11,803,062-15,835,885 , GRCh38.p12 chr12: 11,650,128-15,682,951 LRP6, APOLD1, 78 more genes
    nsv6290802copy number variation1nstd102humanUncertain significance GRCh37 chr12: 12,315,219-12,520,934 , GRCh38.p12 chr12: 12,162,285-12,368,000 , GRCh38.p12 chr12|NW_011332696.1: 131,283-337,002 LRP6, RNU6-318P, 7 more genes
    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
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