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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5926261copy number variation1nstd209human GRCh38 chr10: 87,863,716-87,863,973 , GRCh37.p13 chr10: 89,623,473-89,623,730 KLLN, PTEN
    nsv5911081copy number variation1nstd209human GRCh38 chr10: 87,893,066-87,893,964 , GRCh37.p13 chr10: 89,652,823-89,653,721 PTEN
    nsv5695076mobile element insertion2nstd211human GRCh38 chr10: 87,914,786-87,914,786 , GRCh37.p13 chr10: 89,674,543-89,674,543 PTEN
    nsv5674321insertion1nstd102humanPathogenic GRCh37 chr10: 89,711,944-89,711,944 , GRCh38 chr10: 87,952,187-87,952,187 PTEN
    nsv5672694copy number variation1nstd102humanPathogenic GRCh37 chr10: 89,621,800-89,693,018 , GRCh38.p12 chr10: 87,862,043-87,933,261 , GRCh38.p12 chr10|NW_013171807.1: 77,867-149,053 KLLN, PTEN
    nsv5672610copy number variation1nstd102humanPathogenic GRCh37 chr10: 88,683,123-89,725,321 , GRCh38.p12 chr10: 86,923,366-87,965,564 FAM245A, BMPR1A, 30 more genes
    nsv5672535copy number variation1nstd102humanPathogenic GRCh37 chr10: 89,690,793-89,693,018 , GRCh38.p12 chr10|NW_013171807.1: 146,828-149,053 , GRCh38.p12 chr10: 87,931,036-87,933,261 PTEN
    nsv5672534copy number variation1nstd102humanPathogenic GRCh37 chr10: 89,685,260-89,725,321 , GRCh38.p12 chr10: 87,925,503-87,965,564 , GRCh38.p12 chr10|NW_013171807.1: 141,295-181,353 PTEN, RPL11P3
    nsv5493048copy number variation1nstd206human GRCh38 chr10: 87,936,751-87,936,827 , GRCh37.p13 chr10: 89,696,508-89,696,584 PTEN
    nsv5476911copy number variation1nstd206human GRCh38 chr10: 87,893,068-87,893,965 , GRCh37.p13 chr10: 89,652,825-89,653,722 PTEN
    nsv5409192mobile element insertion1nstd206human GRCh38 chr10: 87,914,770-87,914,770 , GRCh37.p13 chr10: 89,674,527-89,674,527 PTEN
    nsv5380950copy number variation1nstd102humanUncertain significance GRCh37 chr10: 89,624,218-89,624,340 , GRCh38.p12 chr10: 87,864,461-87,864,583 , GRCh38.p12 chr10|NW_013171807.1: 80,284-80,406 PTEN
    nsv5380877copy number variation1nstd102humanUncertain significance GRCh37 chr10: 89,622,083-89,623,527 , GRCh38.p12 chr10: 87,862,326-87,863,770 , GRCh38.p12 chr10|NW_013171807.1: 78,150-79,594 KLLN, PTEN
    nsv5365020translocation1nstd200human GRCh38 chr10: 87,921,462-87,921,462 , GRCh38 chr10: 87,918,289-87,918,289 , GRCh37.p13 chr10: 89,681,219-89,681,219 , GRCh37.p13 chr10: 89,678,046-89,678,046 PTEN
    nsv5317057copy number variation1nstd204human GRCh38.p13 chr10: 87,918,278-87,921,482 , GRCh37.p13 chr10: 89,678,035-89,681,239 PTEN
    nsv5315933copy number variation1nstd204human GRCh38.p13 chr10: 87,893,068-87,893,965 , GRCh37.p13 chr10: 89,652,825-89,653,722 PTEN
    nsv5255439copy number variation1nstd204human GRCh38.p13 chr10: 87,892,852-87,893,985 , GRCh37.p13 chr10: 89,652,609-89,653,742 PTEN
    nsv5247289copy number variation1nstd204human GRCh38.p13 chr10: 87,918,301-87,921,440 , GRCh37.p13 chr10: 89,678,058-89,681,197 PTEN
    nsv5135845mobile element insertion1nstd203human GRCh38 chr10: 87,914,777-87,914,786 , GRCh37.p13 chr10: 89,674,534-89,674,543 PTEN
    nsv5134451mobile element insertion1nstd203human GRCh38 chr10: 87,959,810-87,959,825 , GRCh37.p13 chr10: 89,719,567-89,719,582 PTEN
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