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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137135copy number variation1nstd102humanPathogenic GRCh37 chr14: 88,401,076-94,725,706 , GRCh38.p12 chr14: 87,934,732-94,140,555 LOC100128939, FAM181A-AS1, 104 more genes
    nsv7094351copy number variation1nstd102humanUncertain significance GRCh37 chr14: 90,429,459-97,347,545 , GRCh38.p12 chr14: 89,963,115-96,881,208 FBLN5, CYB5AP3, 135 more genes
    nsv7094350copy number variation1nstd102humanUncertain significance GRCh37 chr14: 90,429,459-94,856,914 , GRCh38.p12 chr14: 89,963,115-94,390,577 LOC105370619, SLC24A4, 78 more genes
    nsv6976102copy number variation1nstd229human GRCh38 chr14: 93,916,065-93,921,872 , GRCh37.p13 chr14: 94,382,411-94,388,218 FAM181A-AS1, FAM181A
    nsv6974818copy number variation1nstd229human GRCh38 chr14: 93,689,101-94,054,300 , GRCh37.p13 chr14: 94,155,447-94,520,646 CCDC197, DDX24, 9 more genes
    nsv6973421copy number variation1nstd229human GRCh38 chr14: 93,903,395-93,911,887 , GRCh37.p13 chr14: 94,369,741-94,378,233 FAM181A-AS1
    nsv6965036copy number variation1nstd229human GRCh38 chr14: 93,895,685-93,932,073 , GRCh37.p13 chr14: 94,362,031-94,398,419 FAM181A, FAM181A-AS1
    nsv6962820copy number variation1nstd229human GRCh38 chr14: 93,916,837-93,921,661 , GRCh37.p13 chr14: 94,383,183-94,388,007 FAM181A, FAM181A-AS1
    nsv6637825copy number variation1nstd102humanPathogenic GRCh37 chr14: 84,537,502-107,285,437 , GRCh38.p12 chr14: 84,071,158-106,877,229 CHGA, SNORD114-26, 676 more genes
    nsv6637462copy number variation1nstd102humanLikely pathogenic GRCh37 chr14: 81,593,708-97,059,276 , GRCh38.p12 chr14: 81,127,364-96,592,939 SERPINA3, BDKRB1, 210 more genes
    nsv6592963inversion1nstd223human GRCh38 chr14: 86,486,184-95,139,000 , GRCh37.p13 chr14: 86,952,528-95,605,337 CCDC88C-DT, RPSAP4, 134 more genes
    nsv6497636copy number variation1nstd223human GRCh38 chr14: 93,916,065-93,921,868 , GRCh37.p13 chr14: 94,382,411-94,388,214 FAM181A, FAM181A-AS1
    nsv6496125copy number variation1nstd223human GRCh38 chr14: 93,907,811-93,909,155 , GRCh37.p13 chr14: 94,374,157-94,375,501 FAM181A-AS1
    nsv6315524copy number variation1nstd102humanPathogenic GRCh37 chr14: 37,671,058-106,985,955 , GRCh38.p12 chr14: 37,201,853-106,530,013 PAPOLA-DT, LOC105378180, 1338 more genes
    nsv6314190copy number variation1nstd102humanPathogenic GRCh37 chr14: 88,345,625-94,773,741 , GRCh38.p12 chr14: 87,879,281-94,140,555 EML5, LOC105370612, 104 more genes
    nsv6309604copy number variation1nstd102humanLikely pathogenic GRCh37 chr14: 93,687,728-95,560,403 , GRCh38.p12 chr14: 93,638,887-95,094,066 , GRCh38.p12 chr14|NT_187601.1: 335,944-1,475,710 SERPINA3, SERPINA6, 43 more genes
    nsv6132940copy number variation1nstd213human GRCh37 chr14: 93,690,000-95,350,001 , GRCh38.p12 chr14: 93,638,887-94,883,664 , GRCh38.p12 chr14|NT_187601.1: 338,216-1,475,710 SERPINA3, ASB2, 40 more genes
    nsv5939964copy number variation1nstd209human GRCh38 chr14: 93,904,932-93,905,019 , GRCh37.p13 chr14: 94,371,278-94,371,365 FAM181A-AS1
    nsv5928455copy number variation1nstd209human GRCh38 chr14: 93,911,209-93,911,574 , GRCh37.p13 chr14: 94,377,555-94,377,920 FAM181A-AS1
    nsv5508625copy number variation1nstd206human GRCh38 chr14: 93,903,373-93,911,905 , GRCh37.p13 chr14: 94,369,719-94,378,251 FAM181A-AS1
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