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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112661copy number variation1nstd102humanPathogenic GRCh37 chr1: 231,407,943-237,289,859 , GRCh38.p12 chr1: 231,272,197-237,126,559 LOC105373207, LOC105373210, 113 more genes
    nsv5886772copy number variation1nstd209human GRCh38 chr1: 236,437,271-236,623,756 , GRCh37.p13 chr1: 236,600,571-236,787,056 , ENO1P1, 4 more genes
    nsv5829559copy number variation1nstd209human GRCh38 chr1: 236,517,706-236,524,624 , GRCh37.p13 chr1: 236,681,006-236,687,924 LGALS8-AS1, LGALS8
    nsv5829410copy number variation1nstd209human GRCh38 chr1: 236,521,725-236,523,924 , GRCh37.p13 chr1: 236,685,025-236,687,224 LGALS8, LGALS8-AS1
    nsv5450897copy number variation1nstd206human GRCh38 chr1: 236,505,900-236,650,119 , GRCh37.p13 chr1: 236,669,200-236,813,419 , LGALS8-AS1, 2 more genes
    nsv5381285copy number variation2nstd102humanUncertain significance GRCh37 chr1: 130,980,840-248,900,000 , GRCh38.p12 chr1: 120,324,463-248,736,699 , DCST1, 2428 more genes
    nsv5298761copy number variation1nstd204human GRCh38.p13 chr1: 236,505,717-236,650,418 , GRCh37.p13 chr1: 236,669,017-236,813,718 , HEATR1, 2 more genes
    nsv5219882copy number variation1nstd204human GRCh38.p13 chr1: 236,505,901-236,649,300 , GRCh37.p13 chr1: 236,669,201-236,812,600 , HEATR1, 2 more genes
    nsv5216154copy number variation1nstd204human GRCh38.p13 chr1: 236,506,197-236,562,948 , GRCh37.p13 chr1: 236,669,497-236,726,248 , HEATR1, 2 more genes
    nsv4906947copy number variation1nstd200human GRCh38 chr1: 236,520,420-236,522,176 , GRCh37.p13 chr1: 236,683,720-236,685,476 LGALS8, LGALS8-AS1
    nsv4904496copy number variation1nstd200human GRCh38 chr1: 236,505,889-236,650,223 , GRCh37.p13 chr1: 236,669,189-236,813,523 , HEATR1, 2 more genes
    nsv4904495copy number variation1nstd200human GRCh38 chr1: 236,500,299-236,522,413 , GRCh37.p13 chr1: 236,663,599-236,685,713 LGALS8-AS1, LGALS8
    nsv4904494copy number variation1nstd200human GRCh38 chr1: 236,437,271-236,623,759 , GRCh37.p13 chr1: 236,600,571-236,787,059 , EDARADD, 4 more genes
    nsv4781525copy number variation1nstd200human GRCh37 chr1: 236,669,180-236,813,531 , GRCh38.p12 chr1: 236,505,880-236,650,231 , LGALS8-AS1, 2 more genes
    nsv4781524copy number variation1nstd200human GRCh37 chr1: 236,600,571-236,787,060 , GRCh38.p12 chr1: 236,437,271-236,623,760 , EDARADD, 4 more genes
    nsv4728561copy number variation1nstd102humanUncertain significance GRCh37 chr1: 235,931,559-236,766,584 , GRCh38.p12 chr1: 235,768,259-236,603,284 RNU5E-2P, ENO1P1, 15 more genes
    nsv4684187copy number variation1nstd102humanPathogenic GRCh37 chr1: 210,152,794-249,218,992 , GRCh38.p12 chr1: 209,979,449-248,924,793 HLX-AS1, OPN3, 740 more genes
    nsv4680590copy number variation1nstd189human GRCh37.p13 chr1: 236,599,474-236,785,876 , GRCh38.p12 chr1: 236,436,174-236,622,576 , ENO1P1, 4 more genes
    nsv4679543copy number variation1nstd189human GRCh37.p13 chr1: 236,610,155-236,778,423 , GRCh38.p12 chr1: 236,446,855-236,615,123 , ENO1P1, 4 more genes
    nsv4674785copy number variation1nstd102humanPathogenic GRCh37 chr1: 219,916,966-239,004,378 , GRCh38.p12 chr1: 219,743,624-238,841,078 RPL23AP23, LOC101927143, 414 more genes
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