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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5898568copy number variation1nstd209human GRCh38 chr5: 134,209,464-134,209,690 , GRCh37.p13 chr5: 133,545,155-133,545,381 PPP2CA
    nsv5890413copy number variation1nstd209human GRCh38 chr5: 134,208,311-134,209,485 , GRCh37.p13 chr5: 133,544,002-133,545,176 PPP2CA
    nsv5682039mobile element insertion1nstd211human GRCh38 chr5: 134,212,454-134,212,454 , GRCh37.p13 chr5: 133,548,145-133,548,145 PPP2CA
    nsv5471810copy number variation1nstd206human GRCh38 chr5: 134,190,499-134,193,513 , GRCh37.p13 chr5: 133,526,190-133,529,204 PPP2CA
    nsv5096875mobile element insertion1nstd203human GRCh38 chr5: 134,212,443-134,212,454 , GRCh37.p13 chr5: 133,548,134-133,548,145 PPP2CA
    nsv5036421inversion1nstd200human GRCh38 chr5: 85,193,812-162,906,830 , GRCh37.p13 chr5: 84,489,630-162,333,836 , PRR16, 1116 more genes
    nsv5034346inversion1nstd200human GRCh38 chr5: 99,223,339-135,778,784 , GRCh37.p13 chr5: 98,559,043-135,114,473 , NUDT12, 438 more genes
    nsv4947215copy number variation1nstd200human GRCh38 chr5: 93,957,557-155,223,076 , GRCh37.p13 chr5: 93,293,262-154,602,636 , TGFBI, 937 more genes
    nsv4938666copy number variation1nstd200human GRCh38 chr5: 134,190,489-134,193,542 , GRCh37.p13 chr5: 133,526,180-133,529,233 PPP2CA
    nsv4885569inversion1nstd200human GRCh37 chr5: 84,489,636-162,333,841 , GRCh38.p12 chr5: 85,193,818-162,906,835 , UBE2B, 1116 more genes
    nsv4804031copy number variation1nstd200human GRCh37 chr5: 133,551,913-133,553,152 , GRCh38.p12 chr5: 134,216,222-134,217,461 PPP2CA
    nsv4804030copy number variation1nstd200human GRCh37 chr5: 133,545,157-133,545,382 , GRCh38.p12 chr5: 134,209,466-134,209,691 PPP2CA
    nsv4549179insertion1nstd166human GRCh37.p13 chr5: 133,548,134-133,548,134 , GRCh38.p12 chr5: 134,212,443-134,212,443 PPP2CA
    nsv4485386mobile element insertion1nstd166human GRCh37.p13 chr5: 133,548,870-133,548,870 , GRCh38.p12 chr5: 134,213,179-134,213,179 PPP2CA
    nsv4436202copy number variation1nstd102humanUncertain significance GRCh37 chr5: 14,685,137-149,511,942 , GRCh38.p12 chr5: 14,685,028-150,132,379 RNU1-150P, RNU6-727P, 1757 more genes
    nsv4320566inversion1nstd166human GRCh37.p13 chr5: 114,283,102-148,759,757 , GRCh38.p12 chr5: 114,947,405-149,380,194 , ACTBP4, 606 more genes
    nsv4129736copy number variation1nstd166human GRCh37.p13 chr5: 133,543,485-133,543,611 , GRCh38.p12 chr5: 134,207,794-134,207,920 PPP2CA
    nsv3971975copy number variation1nstd102humanLikely pathogenic GRCh37 chr5: 126,377,719-136,270,989 , GRCh38.p12 chr5: 127,042,027-136,935,300 ACTBP4, CAMLG, 157 more genes
    nsv3924484copy number variation1nstd102humanPathogenic NCBI36 chr5: 132,894,824-134,211,267 , GRCh38 chr5: 133,531,234-134,847,678 , GRCh37 chr5: 132,866,925-134,183,368 C5orf24, UBE2B, 28 more genes
    nsv3923830copy number variation1nstd102humanPathogenic GRCh37 chr5: 132,151,895-134,718,848 , GRCh38 chr5: 132,816,203-135,383,158 , NCBI36 chr5: 132,179,794-134,746,747 MTND5P11, TCF7, 60 more genes
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