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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
    nsv7064011inversion1nstd229human GRCh38 chr12: 11,255,910-17,864,916 , GRCh37.p13 chr12: 11,408,826-18,017,850 MGP, MIR3974, 108 more genes
    nsv6928982copy number variation1nstd229human GRCh38 chr12: 14,778,501-14,782,700 , GRCh37.p13 chr12: 14,931,435-14,935,634 WBP11, C12orf60, 1 more genes
    nsv6928560copy number variation1nstd229human GRCh38 chr12: 14,801,426-14,802,139 , GRCh37.p13 chr12: 14,954,360-14,955,073 C12orf60, WBP11
    nsv6927487copy number variation1nstd229human GRCh38 chr12: 14,792,455-14,792,574 , GRCh37.p13 chr12: 14,945,389-14,945,508 C12orf60, WBP11
    nsv6927380copy number variation1nstd229human GRCh38 chr12: 14,349,276-14,787,271 , GRCh37.p13 chr12: 14,502,210-14,940,205 PLBD1, C12orf60, 10 more genes
    nsv6922706copy number variation1nstd229human GRCh38 chr12: 14,784,401-14,801,800 , GRCh37.p13 chr12: 14,937,335-14,954,734 WBP11, C12orf60
    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
    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
    nsv6309308copy number variation1nstd102humanUncertain significance GRCh37 chr12: 14,849,146-15,669,910 , GRCh38.p12 chr12: 14,696,212-15,516,976 PTPRO, RERG, 17 more genes
    nsv6240695mobile element insertion1nstd215human GRCh38 chr12: 14,787,589-14,787,589 , GRCh37.p13 chr12: 14,940,523-14,940,523 WBP11, C12orf60
    nsv6205164copy number variation1nstd214human GRCh38 chr12: 14,792,452-14,792,573 , GRCh37.p13 chr12: 14,945,386-14,945,507 C12orf60, WBP11
    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
    nsv6132422copy number variation1nstd213human GRCh37 chr12: 190,000-30,830,001 , GRCh38.p12 chr12: 80,834-30,677,067 , A2M, 622 more genes
    nsv6132418copy number variation1nstd213human GRCh37 chr12: 14,930,000-15,180,001 , GRCh38.p12 chr12: 14,777,066-15,027,067 ARHGDIB, ART4, 8 more genes
    nsv6132416copy number variation1nstd213human GRCh37 chr12: 13,780,000-20,840,001 , GRCh38.p12 chr12: 13,627,066-20,687,067 ARHGDIB, ART4, 87 more genes
    nsv6132215copy number variation1nstd213human GRCh37 chr12: 11,360,000-16,150,001 , GRCh38.p12 chr12: 11,207,094-15,997,067 ARHGDIB, ART4, 93 more genes
    nsv6132138copy number variation1nstd213human GRCh37 chr12: 11,250,000-19,950,001 , GRCh38.p12 chr12: 11,097,401-19,797,067 ARHGDIB, ART4, 139 more genes
    nsv6081147insertion1nstd212human GRCh38 chr12: 14,787,585-14,787,585 , GRCh37.p13 chr12: 14,940,519-14,940,519 WBP11, C12orf60
    nsv6022109copy number variation1nstd212human GRCh38 chr12: 14,792,452-14,792,574 , GRCh37.p13 chr12: 14,945,386-14,945,508 C12orf60, WBP11
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