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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112778copy number variation1nstd102humanPathogenic GRCh37 chr20: 51,799,648-62,916,626 , GRCh38.p12 chr20: 53,183,109-64,285,273 LINC01742, MTCO2P1, 253 more genes
    nsv5673415copy number variation1nstd102humanLikely benign GRCh38 chr20: 63,685,601-63,685,678 , GRCh37 chr20: 62,316,954-62,317,031 RTEL1-TNFRSF6B, RTEL1
    nsv5673331copy number variation2nstd102humanPathogenic, Likely pathogenic GRCh37 chr20: 62,298,812-62,298,916 , GRCh38.p12 chr20: 63,667,459-63,667,563 RTEL1-TNFRSF6B, RTEL1
    nsv5673330copy number variation1nstd102humanPathogenic GRCh37 chr20: 62,290,746-62,290,867 , GRCh38.p12 chr20: 63,659,393-63,659,514 RTEL1, RTEL1-TNFRSF6B
    nsv5673258copy number variation2nstd102humanLikely pathogenic GRCh37 chr20: 62,316,913-62,316,990 , GRCh38 chr20: 63,685,560-63,685,637 RTEL1, RTEL1-TNFRSF6B
    nsv5673183copy number variation1nstd102humanLikely pathogenic GRCh37 chr20: 62,292,641-62,327,221 , GRCh38.p12 chr20: 63,661,288-63,695,868 TNFRSF6B, RTEL1, 1 more genes
    nsv5673182copy number variation1nstd102humanPathogenic GRCh37 chr20: 62,290,746-62,312,082 , GRCh38.p12 chr20: 63,659,393-63,680,729 RTEL1-TNFRSF6B, RTEL1
    nsv5673181copy number variation1nstd102humanPathogenic GRCh37 chr20: 62,076,002-62,324,646 , GRCh38.p12 chr20: 63,444,649-63,693,293 PPDPF, LOC105372725, 13 more genes
    nsv5671614insertion1nstd207human GRCh38 chr20: 63,682,229-63,682,229 , GRCh37.p13 chr20: 62,313,582-62,313,582 RTEL1-TNFRSF6B, RTEL1
    nsv5669765insertion1nstd207human GRCh38 chr20: 63,669,874-63,669,874 , GRCh37.p13 chr20: 62,301,227-62,301,227 RTEL1-TNFRSF6B, RTEL1
    nsv5668996insertion1nstd207human GRCh38 chr20: 63,677,697-63,677,697 , GRCh37.p13 chr20: 62,309,050-62,309,050 RTEL1-TNFRSF6B, RTEL1
    nsv5668816insertion1nstd207human GRCh38 chr20: 63,669,630-63,669,630 , GRCh37.p13 chr20: 62,300,983-62,300,983 RTEL1-TNFRSF6B, RTEL1
    nsv5668615insertion1nstd207human GRCh38 chr20: 63,674,129-63,674,129 , GRCh37.p13 chr20: 62,305,482-62,305,482 RTEL1, RTEL1-TNFRSF6B
    nsv5668277insertion1nstd207human GRCh38 chr20: 63,693,681-63,693,681 , GRCh37.p13 chr20: 62,325,034-62,325,034 RTEL1-TNFRSF6B, RTEL1
    nsv5667686insertion1nstd207human GRCh38 chr20: 63,669,644-63,669,644 , GRCh37.p13 chr20: 62,300,997-62,300,997 RTEL1-TNFRSF6B, RTEL1
    nsv5666247insertion1nstd207human GRCh38 chr20: 63,693,462-63,693,462 , GRCh37.p13 chr20: 62,324,815-62,324,815 RTEL1-TNFRSF6B, RTEL1
    nsv5665159insertion1nstd207human GRCh38 chr20: 63,693,732-63,693,732 , GRCh37.p13 chr20: 62,325,085-62,325,085 RTEL1-TNFRSF6B, RTEL1
    nsv5599963copy number variation1nstd207human GRCh38 chr20: 63,677,697-63,677,843 , GRCh37.p13 chr20: 62,309,050-62,309,196 RTEL1-TNFRSF6B, RTEL1
    nsv5599421copy number variation1nstd207human GRCh38 chr20: 63,669,644-63,669,814 , GRCh37.p13 chr20: 62,300,997-62,301,167 RTEL1, RTEL1-TNFRSF6B
    nsv5594187copy number variation1nstd207human GRCh38 chr20: 63,669,644-63,670,042 , GRCh37.p13 chr20: 62,300,997-62,301,395 RTEL1-TNFRSF6B, RTEL1
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