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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5930047copy number variation1nstd209human GRCh38 chr14: 35,042,551-35,131,102 , GRCh37.p13 chr14: 35,511,757-35,600,308 PRORP, PPP2R3C, 2 more genes
    nsv5867071copy number variation1nstd209human GRCh38 chr14: 35,065,692-35,070,591 , GRCh37.p13 chr14: 35,534,898-35,539,797 FAM177A1
    nsv5863139copy number variation2nstd209human GRCh38 chr14: 35,081,589-35,083,817 , GRCh37.p13 chr14: 35,550,795-35,553,023 PPP2R3C, LOC101927178, 1 more genes
    nsv5860495copy number variation1nstd209human GRCh38 chr14: 35,045,008-35,062,496 , GRCh37.p13 chr14: 35,514,214-35,531,702 FAM177A1
    nsv5860447copy number variation2nstd209human GRCh38 chr14: 35,058,111-35,059,318 , GRCh37.p13 chr14: 35,527,317-35,528,524 FAM177A1
    nsv5855622copy number variation1nstd209human GRCh38 chr14: 35,050,846-35,052,545 , GRCh37.p13 chr14: 35,520,052-35,521,751 FAM177A1
    nsv5672809copy number variation1nstd102humanLikely pathogenic GRCh37 chr14: 35,513,595-35,521,682 , GRCh38 chr14: 35,044,389-35,052,476 FAM177A1
    nsv5498015copy number variation1nstd206human GRCh38 chr14: 34,191,713-38,057,713 , GRCh37.p13 chr14: 34,660,919-38,526,918 , RPL23AP71, 79 more genes
    nsv5495817copy number variation1nstd206human GRCh38 chr14: 35,046,628-35,050,029 , GRCh37.p13 chr14: 35,515,834-35,519,235 FAM177A1
    nsv5381757copy number variation1nstd102humanPathogenic GRCh37 chr14: 33,608,925-44,570,367 , GRCh38.p12 chr14: 33,139,719-44,101,164 RPLP0P3, KRT18P6, 131 more genes
    nsv5143475mobile element insertion1nstd203human GRCh38 chr14: 35,076,667-35,076,680 , GRCh37.p13 chr14: 35,545,873-35,545,886 FAM177A1
    nsv5059977copy number variation1nstd102humanLikely pathogenic GRCh37 chr14: 35,546,986-35,556,772 , GRCh38 chr14: 35,077,780-35,087,566 PPP2R3C, FAM177A1, 1 more genes
    nsv4998687copy number variation1nstd200human GRCh38 chr14: 35,083,528-35,084,674 , GRCh37.p13 chr14: 35,552,734-35,553,880 LOC101927178, FAM177A1, 1 more genes
    nsv4998686copy number variation1nstd200human GRCh38 chr14: 35,044,342-35,052,423 , GRCh37.p13 chr14: 35,513,548-35,521,629 FAM177A1
    nsv4994197copy number variation1nstd200human GRCh38 chr14: 35,058,752-35,256,240 , GRCh37.p13 chr14: 35,527,958-35,725,446 FAM177A1, SEPTIN7P1, 7 more genes
    nsv4994196copy number variation1nstd200human GRCh38 chr14: 35,048,948-35,290,352 , GRCh37.p13 chr14: 35,518,154-35,759,558 RPL9P3, FAM177A1, 9 more genes
    nsv4994195copy number variation1nstd200human GRCh38 chr14: 35,027,565-35,047,768 , GRCh37.p13 chr14: 35,496,771-35,516,974 SRP54, FAM177A1
    nsv4994194copy number variation1nstd200human GRCh38 chr14: 34,995,494-35,156,698 , GRCh37.p13 chr14: 35,464,700-35,625,904 PPP2R3C, FAM177A1, 5 more genes
    nsv4994192copy number variation1nstd200human GRCh38 chr14: 34,924,660-35,315,430 , GRCh37.p13 chr14: 35,393,866-35,784,636 DPRXP3, LOC101927178, 12 more genes
    nsv4994191copy number variation1nstd200human GRCh38 chr14: 34,912,831-35,077,153 , GRCh37.p13 chr14: 35,382,037-35,546,359 FAM177A1, IGBP1P1, 2 more genes
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