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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112765copy number variation1nstd102humanPathogenic GRCh37 chr10: 118,247,181-135,435,319 , GRCh38.p12 chr10: 116,487,669-133,621,815 STK32C, LOC105378542, 266 more genes
    nsv5974601insertion1nstd209human GRCh38 chr10: 119,665,093-119,665,093 , GRCh37.p13 chr10: 121,424,605-121,424,605 BAG3
    nsv5907810copy number variation1nstd209human GRCh38 chr10: 119,651,226-119,651,298 , GRCh37.p13 chr10: 121,410,738-121,410,810 BAG3
    nsv5672606copy number variation1nstd102humanPathogenic GRCh37 chr10: 121,411,178-121,437,012 , GRCh38.p12 chr10: 119,651,666-119,677,500 BAG3
    nsv5672603copy number variation1nstd102humanLikely pathogenic GRCh37 chr10: 119,302,758-124,813,305 , GRCh38.p12 chr10: 117,543,247-123,053,789 ACADSB, DMBT1, 84 more genes
    nsv5632772insertion1nstd207human GRCh38 chr10: 119,675,902-119,675,902 , GRCh37.p13 chr10: 121,435,414-121,435,414 BAG3
    nsv5629610insertion1nstd207human GRCh38 chr10: 119,675,872-119,675,872 , GRCh37.p13 chr10: 121,435,384-121,435,384 BAG3
    nsv5564284copy number variation1nstd102humanUncertain significance GRCh37 chr10: 121,429,353-121,429,699 , GRCh38.p12 chr10: 119,669,841-119,670,187 BAG3
    nsv5513190copy number variation1nstd206human GRCh38 chr10: 119,652,300-119,655,538 , GRCh37.p13 chr10: 121,411,812-121,415,050 BAG3
    nsv5504357copy number variation1nstd206human GRCh38 chr10: 119,652,317-119,659,534 , GRCh37.p13 chr10: 121,411,829-121,419,046 BAG3
    nsv5503299copy number variation1nstd206human GRCh38 chr10: 119,652,195-119,652,258 , GRCh37.p13 chr10: 121,411,707-121,411,770 BAG3
    nsv5501306copy number variation1nstd206human GRCh38 chr10: 119,675,848-119,675,904 , GRCh37.p13 chr10: 121,435,360-121,435,416 BAG3
    nsv5380787copy number variation1nstd102humanUncertain significance GRCh37 chr10: 121,429,353-121,437,012 , GRCh38.p12 chr10: 119,669,841-119,677,500 BAG3
    nsv5380710copy number variation1nstd102humanUncertain significance GRCh37 chr10: 121,411,168-121,429,709 , GRCh38.p12 chr10: 119,651,656-119,670,197 BAG3
    nsv4762553insertion1nstd199human GRCh37 chr10: 121,435,391-121,435,391 , GRCh38.p12 chr10: 119,675,879-119,675,879 BAG3
    nsv4675991copy number variation1nstd102humanPathogenic GRCh37 chr10: 119,996,339-135,427,143 , GRCh38.p12 chr10: 118,236,827-133,613,639 STK32C, LOC105378542, 237 more genes
    nsv4547746insertion1nstd166human GRCh37.p13 chr10: 121,435,331-121,435,331 , GRCh38.p12 chr10: 119,675,819-119,675,819 BAG3
    nsv4546841insertion1nstd166human GRCh37.p13 chr10: 121,435,293-121,435,293 , GRCh38.p12 chr10: 119,675,781-119,675,781 BAG3
    nsv4456626copy number variation1nstd102humanPathogenic GRCh37 chr10: 114,544,537-135,427,143 , GRCh38.p12 chr10: 112,784,778-133,613,639 LOC105378521, ZRANB1, 317 more genes
    nsv4454453copy number variation1nstd102humanPathogenic GRCh38 chr10: 119,676,454-119,677,500 , GRCh37 chr10: 121,435,966-121,437,012 BAG3
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