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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3882838copy number variation1nstd102humannot provided GRCh37 chr19: 35,587,635-35,600,510 , GRCh38 chr19: 35,096,731-35,109,606 HPN-AS1
    nsv3877116copy number variation1nstd102humannot provided GRCh37 chr19: 35,587,635-35,597,215 , GRCh38 chr19: 35,096,731-35,106,311 HPN-AS1
    nsv6519128copy number variation1nstd223human GRCh38 chr19: 35,052,292-35,053,473 , GRCh37.p13 chr19: 35,543,196-35,544,377 HPN
    nsv6529578copy number variation1nstd223human GRCh38 chr19: 35,056,253-35,056,696 , GRCh37.p13 chr19: 35,547,157-35,547,600 HPN
    nsv5520409copy number variation1nstd206human GRCh38 chr19: 35,056,258-35,056,696 , GRCh37.p13 chr19: 35,547,162-35,547,600 HPN
    nsv6208383copy number variation1nstd214human GRCh38 chr19: 35,105,964-35,106,050 , GRCh37.p13 chr19: 35,596,868-35,596,954 HPN-AS1
    nsv6282054copy number variation1nstd214human GRCh38 chr19: 35,105,958-35,106,042 , GRCh37.p13 chr19: 35,596,862-35,596,946 HPN-AS1
    nsv6221199copy number variation1nstd214human GRCh38 chr19: 35,045,650-35,045,718 , GRCh37.p13 chr19: 35,536,554-35,536,622 HPN
    nsv6219257copy number variation1nstd214human GRCh38 chr19: 35,045,739-35,045,807 , GRCh37.p13 chr19: 35,536,643-35,536,711 HPN
    nsv6212460copy number variation1nstd214human GRCh38 chr19: 35,045,700-35,045,768 , GRCh37.p13 chr19: 35,536,604-35,536,672 HPN
    nsv6055960copy number variation1nstd212human GRCh38 chr19: 35,095,599-35,095,860 , GRCh37.p13 chr19: 35,586,503-35,586,764 HPN-AS1
    nsv6053464copy number variation1nstd212human GRCh38 chr19: 35,055,561-35,055,782 , GRCh37.p13 chr19: 35,546,465-35,546,686 HPN
    nsv6056131copy number variation1nstd212human GRCh38 chr19: 35,105,439-35,105,601 , GRCh37.p13 chr19: 35,596,343-35,596,505 HPN-AS1
    nsv6041634copy number variation1nstd212human GRCh38 chr19: 35,045,673-35,045,741 , GRCh37.p13 chr19: 35,536,577-35,536,645 HPN
    nsv6059392copy number variation1nstd212human GRCh38 chr19: 35,105,988-35,106,046 , GRCh37.p13 chr19: 35,596,892-35,596,950 HPN-AS1
    nsv6041689copy number variation1nstd212human GRCh38 chr19: 35,105,958-35,106,016 , GRCh37.p13 chr19: 35,596,862-35,596,920 HPN-AS1
    nsv4749490copy number variation1nstd199human GRCh37 chr19: 35,536,583-35,536,651 , GRCh38.p12 chr19: 35,045,679-35,045,747 HPN
    nsv5597521copy number variation1nstd207human GRCh38 chr19: 35,045,650-35,045,718 , GRCh37.p13 chr19: 35,536,554-35,536,622 HPN
    nsv5020441copy number variation1nstd200human GRCh38 chr19: 35,102,442-35,112,980 , GRCh37.p13 chr19: 35,593,346-35,603,884 HPN-AS1
    nsv5027685copy number variation1nstd200human GRCh38 chr19: 35,052,292-35,053,473 , GRCh37.p13 chr19: 35,543,196-35,544,377 HPN
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