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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6121750copy number variation1nstd186human GRCh37 chr16: 16,329,757-16,363,857 , GRCh38.p12 chr16|NT_187607.1: 1,893,898-1,928,003 , GRCh38.p12 chr16: 16,235,900-16,270,000 NOMO3
    nsv6120739copy number variation1nstd186human GRCh37 chr16: 16,329,857-16,339,857 , GRCh38.p12 chr16|NT_187607.1: 1,893,998-1,903,998 , GRCh38.p12 chr16: 16,236,000-16,246,000 NOMO3
    nsv5967951inversion1nstd209human GRCh38 chr16: 13,469,401-22,726,308 , GRCh37.p13 chr16: 13,563,258-22,737,629 , ABCC6, 214 more genes
    nsv5936799copy number variation1nstd209human GRCh38 chr16: 16,237,730-16,243,714 , GRCh37.p13 chr16: 16,331,587-16,337,571 NOMO3
    nsv5928138copy number variation1nstd209human GRCh38 chr16: 15,180,124-18,091,718 , GRCh37.p13 chr16: 15,273,981-18,185,575 , LOC102723692, 42 more genes
    nsv5885821copy number variation2nstd209human GRCh38 chr16: 16,235,510-16,237,513 , GRCh37.p13 chr16: 16,329,367-16,331,370 NOMO3
    nsv5868221copy number variation2nstd209human GRCh38 chr16: 16,236,452-16,239,299 , GRCh37.p13 chr16: 16,330,309-16,333,156 NOMO3
    nsv5662015insertion1nstd207human GRCh38 chr16: 16,235,497-16,235,497 , GRCh37.p13 chr16: 16,329,354-16,329,354 NOMO3
    nsv5649808insertion1nstd207human GRCh38 chr16: 16,235,503-16,235,503 , GRCh37.p13 chr16: 16,329,360-16,329,360 NOMO3
    nsv5602458copy number variation1nstd207human GRCh38 chr16: 16,272,605-16,272,742 , GRCh37.p13 chr16: 16,366,462-16,366,599 NOMO3
    nsv5531850copy number variation1nstd206human GRCh38 chr16: 16,235,900-16,270,000 , GRCh37.p13 chr16: 16,329,757-16,363,857 NOMO3
    nsv5528524copy number variation1nstd206human GRCh38 chr16: 16,236,000-16,246,000 , GRCh37.p13 chr16: 16,329,857-16,339,857 NOMO3
    nsv5380983copy number variation1nstd102humanPathogenic GRCh37 chr16: 14,968,859-16,363,239 , GRCh38.p12 chr16: 14,875,002-16,269,382 , GRCh38.p12 chr16|NT_187607.1: 531,831-1,927,385 LOC102724984, LOC728138, 50 more genes
    nsv5279943copy number variation1nstd204human GRCh38.p13 chr16: 16,234,501-16,271,300 , GRCh37.p13 chr16: 16,328,358-16,365,157 NOMO3
    nsv5279461copy number variation1nstd204human GRCh38.p13 chr16: 16,243,449-16,244,525 , GRCh37.p13 chr16: 16,337,306-16,338,382 NOMO3
    nsv5278571copy number variation1nstd204human GRCh38.p13 chr16: 16,265,329-16,266,767 , GRCh37.p13 chr16: 16,359,186-16,360,624 NOMO3
    nsv5277829copy number variation1nstd204human GRCh38.p13 chr16: 16,254,428-16,255,723 , GRCh37.p13 chr16: 16,348,285-16,349,580 NOMO3
    nsv5277719copy number variation1nstd204human GRCh38.p13 chr16: 16,231,101-16,248,600 , GRCh37.p13 chr16: 16,324,958-16,342,457 NOMO3
    nsv5277147copy number variation1nstd204human GRCh38.p13 chr16: 16,248,301-16,255,500 , GRCh37.p13 chr16: 16,342,158-16,349,357 NOMO3
    nsv5274699copy number variation1nstd204human GRCh38.p13 chr16: 16,230,401-16,271,200 , GRCh37.p13 chr16: 16,324,258-16,365,057 NOMO3
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