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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5975122insertion1nstd209human GRCh38 chr12: 32,865,681-32,865,681 , GRCh37.p13 chr12: 33,018,615-33,018,615 PKP2
    nsv5970579insertion1nstd209human GRCh38 chr12: 32,846,745-32,846,745 , GRCh37.p13 chr12: 32,999,679-32,999,679 PKP2
    nsv5923369copy number variation1nstd209human GRCh38 chr12: 32,803,983-32,804,032 , GRCh37.p13 chr12: 32,956,917-32,956,966 PKP2
    nsv5919006copy number variation1nstd209human GRCh38 chr12: 32,810,665-32,810,979 , GRCh37.p13 chr12: 32,963,599-32,963,913 PKP2
    nsv5918712copy number variation1nstd209human GRCh38 chr12: 32,831,599-32,834,600 , GRCh37.p13 chr12: 32,984,533-32,987,534 PKP2
    nsv5908610copy number variation1nstd209human GRCh38 chr12: 32,787,129-32,790,635 , GRCh37.p13 chr12: 32,940,063-32,943,569 PKP2
    nsv5867011copy number variation1nstd209human GRCh38 chr12: 32,787,494-32,790,799 , GRCh37.p13 chr12: 32,940,428-32,943,733 PKP2
    nsv5859932copy number variation1nstd209human GRCh38 chr12: 32,807,795-32,810,544 , GRCh37.p13 chr12: 32,960,729-32,963,478 PKP2
    nsv5853300copy number variation1nstd209human GRCh38 chr12: 32,831,561-32,834,642 , GRCh37.p13 chr12: 32,984,495-32,987,576 PKP2
    nsv5719885mobile element insertion1nstd211human GRCh38 chr12: 32,871,173-32,871,173 , GRCh37.p13 chr12: 33,024,107-33,024,107 PKP2
    nsv5706917mobile element insertion2nstd211human GRCh38 chr12: 32,816,962-32,816,962 , GRCh37.p13 chr12: 32,969,896-32,969,896 PKP2
    nsv5697856mobile element insertion2nstd211human GRCh38 chr12: 32,864,052-32,864,052 , GRCh37.p13 chr12: 33,016,986-33,016,986 PKP2
    nsv5674295inversion1nstd102humanPathogenic GRCh38 chr12: 32,841,995-32,850,927 , GRCh37 chr12: 32,994,929-33,003,861 PKP2
    nsv5672792copy number variation1nstd102humanPathogenic GRCh37 chr12: 32,949,033-32,955,500 , GRCh38.p12 chr12: 32,796,099-32,802,566 PKP2
    nsv5672717copy number variation1nstd102humanLikely pathogenic GRCh37 chr12: 32,949,033-32,949,242 , GRCh38.p12 chr12: 32,796,099-32,796,308 PKP2
    nsv5672644copy number variation1nstd102humanPathogenic GRCh37 chr12: 33,021,851-33,031,976 , GRCh38.p12 chr12: 32,868,917-32,879,042 PKP2
    nsv5672561copy number variation1nstd102humanPathogenic GRCh37 chr12: 33,030,760-33,031,986 , GRCh38.p12 chr12: 32,877,826-32,879,052 PKP2
    nsv5595156copy number variation1nstd207human GRCh38 chr12: 32,810,665-32,810,979 , GRCh37.p13 chr12: 32,963,599-32,963,913 PKP2
    nsv5593752copy number variation1nstd207human GRCh38 chr12: 32,858,085-32,858,134 , GRCh37.p13 chr12: 33,011,019-33,011,068 PKP2
    nsv5564293copy number variation1nstd102humanUncertain significance GRCh37 chr12: 32,772,622-33,049,675 , GRCh38.p12 chr12: 32,619,688-32,896,741 PKP2, LOC100420981, 4 more genes
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