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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5939677copy number variation1nstd209human GRCh38 chr12: 102,156,231-102,236,309 , GRCh37.p13 chr12: 102,550,009-102,630,087 PMCH, PARPBP, 2 more genes
    nsv5866920copy number variation1nstd209human GRCh38 chr12: 102,185,631-102,197,330 , GRCh37.p13 chr12: 102,579,409-102,591,108 PARPBP, PMCH
    nsv5862897copy number variation2nstd209human GRCh38 chr12: 102,197,631-102,198,830 , GRCh37.p13 chr12: 102,591,409-102,592,608 PARPBP, PMCH
    nsv5862831copy number variation1nstd209human GRCh38 chr12: 102,194,731-102,198,030 , GRCh37.p13 chr12: 102,588,509-102,591,808 PARPBP, PMCH
    nsv5271616copy number variation1nstd204human GRCh38.p13 chr12: 102,193,901-102,202,000 , GRCh37.p13 chr12: 102,587,679-102,595,778 PARPBP, PMCH
    nsv5037136inversion1nstd200human GRCh38 chr12: 69,787,024-109,882,221 , GRCh37.p13 chr12: 70,180,804-110,320,026 , RPL23AP68, 540 more genes
    nsv4995329copy number variation1nstd200human GRCh38 chr12: 102,171,717-102,217,919 , GRCh37.p13 chr12: 102,565,495-102,611,697 RN7SL793P, PARPBP, 1 more genes
    nsv4886161inversion1nstd200human GRCh37 chr12: 70,180,810-110,320,027 , GRCh38.p12 chr12: 69,787,030-109,882,222 , LOC728739, 540 more genes
    nsv4835575copy number variation1nstd200human GRCh37 chr12: 102,565,495-102,611,697 , GRCh38.p12 chr12: 102,171,717-102,217,919 RN7SL793P, PARPBP, 1 more genes
    nsv4755205inversion1nstd199human GRCh37 chr12: 25,956,127-125,801,151 , GRCh38.p12 chr12: 25,803,193-125,316,605 , ACACB, 1787 more genes
    nsv4736781copy number variation1nstd199human GRCh37 chr12: 25,957,322-125,801,148 , GRCh38.p12 chr12: 25,804,388-125,316,602 , RNA5SP368, 1787 more genes
    nsv4728941copy number variation1nstd102humanUncertain significance GRCh37 chr12: 102,583,458-102,711,311 , GRCh38.p12 chr12: 102,189,680-102,317,533 LINC02456, PMCH, 3 more genes
    nsv4680088copy number variation1nstd189human GRCh37.p13 chr12: 102,055,253-102,714,201 , GRCh38.p12 chr12: 101,661,475-102,320,423 MYBPC1, PMCH, 21 more genes
    nsv4675271copy number variation1nstd102humanUncertain significance GRCh37 chr12: 101,953,283-102,683,945 , GRCh38.p12 chr12: 101,559,505-102,290,167 DRAM1, RNU6-172P, 23 more genes
    nsv4609339copy number variation1nstd183human GRCh37 chr12: 102,589,037-102,589,685 , GRCh38.p12 chr12: 102,195,259-102,195,907 PMCH, PARPBP
    nsv4456580copy number variation1nstd102humanUncertain significance GRCh37 chr12: 102,414,522-105,845,768 , GRCh38.p12 chr12: 102,020,744-105,451,990 HCFC2, MIR3652, 50 more genes
    nsv4456033copy number variation1nstd102humanUncertain significance GRCh37 chr12: 101,447,925-102,593,349 , GRCh38.p12 chr12: 101,054,147-102,199,571 RPS27P23, PMCH, 33 more genes
    nsv4456023copy number variation1nstd102humanUncertain significance GRCh37 chr12: 102,116,591-102,607,083 , GRCh38.p12 chr12: 101,722,813-102,213,305 RNU6-172P, PARPBP, 16 more genes
    nsv4382272copy number variation1nstd173human GRCh37 chr12: 102,573,001-102,689,637 , GRCh38.p12 chr12: 102,179,223-102,295,859 PMCH, RN7SL793P, 3 more genes
    nsv4325802inversion1nstd166human GRCh37.p13 chr12: 70,180,810-110,320,028 , GRCh38.p12 chr12: 69,787,030-109,882,223 , APAF1, 540 more genes
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