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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148186copy number variation1nstd102humanUncertain significance GRCh37 chr20: 52,773,668-62,965,020 , GRCh38.p12 chr20: 54,157,129-64,333,667 LOC105372717, CTCFL, 245 more genes
    nsv7148178copy number variation1nstd102humanPathogenic GRCh38 chr20: 62,632,017-63,794,804 , GRCh37.p13 chr20: 61,267,734-62,426,157 GID8, TCFL5, 60 more genes
    nsv7096264copy number variation2nstd102humanUncertain significance GRCh37 chr20: 60,831,241-62,680,869 , GRCh38.p12 chr20: 62,256,185-64,049,516 RPS21, MIR1-1HG, 102 more genes
    nsv7095910copy number variation1nstd102humanPathogenic GRCh37 chr20: 61,471,874-62,078,210 , GRCh38.p12 chr20: 62,840,522-63,446,857 LINC01749, HAR1A, 32 more genes
    nsv7061289inversion1nstd229human GRCh38 chr20: 63,026,492-64,008,482 , GRCh37.p13 chr20: 61,657,844-62,639,835 TNFRSF6B, MIR941-5, 60 more genes
    nsv7059476inversion1nstd229human GRCh38 chr20: 63,024,183-64,005,567 , GRCh37.p13 chr20: 61,655,535-62,636,920 RTEL1-TNFRSF6B, LOC105372721, 60 more genes
    nsv7037913copy number variation1nstd229human GRCh38 chr20: 63,331,860-63,338,081 , GRCh37.p13 chr20: 61,963,212-61,969,433 COL20A1, RNU6-994P
    nsv7037078copy number variation1nstd229human GRCh38 chr20: 54,988,450-63,850,628 , GRCh37.p13 chr20: 53,604,989-62,481,981 , RPL39P, 209 more genes
    nsv7036284copy number variation1nstd229human GRCh38 chr20: 63,311,982-63,349,320 , GRCh37.p13 chr20: 61,943,334-61,980,672 COL20A1, CHRNA4, 1 more genes
    nsv7034875copy number variation1nstd229human GRCh38 chr20: 63,325,597-63,328,648 , GRCh37.p13 chr20: 61,956,949-61,960,000 COL20A1
    nsv7032296copy number variation1nstd229human GRCh38 chr20: 63,319,667-63,333,129 , GRCh37.p13 chr20: 61,951,019-61,964,481 COL20A1
    nsv7031457copy number variation1nstd229human GRCh38 chr20: 63,307,491-63,324,904 , GRCh37.p13 chr20: 61,938,843-61,956,256 COL20A1
    nsv7031003copy number variation1nstd229human GRCh38 chr20: 63,305,401-63,492,900 , GRCh37.p13 chr20: 61,936,753-62,124,253 RNU6-994P, LOC105372724, 7 more genes
    nsv7030984copy number variation1nstd229human GRCh38 chr20: 63,320,300-63,326,999 , GRCh37.p13 chr20: 61,951,652-61,958,351 COL20A1
    nsv7030082copy number variation1nstd229human GRCh38 chr20: 63,291,998-63,297,416 , GRCh37.p13 chr20: 61,923,350-61,928,768 COL20A1
    nsv7028159copy number variation1nstd229human GRCh38 chr20: 63,311,795-63,314,677 , GRCh37.p13 chr20: 61,943,147-61,946,029 COL20A1
    nsv7027403copy number variation1nstd229human GRCh38 chr20: 63,322,804-63,400,606 , GRCh37.p13 chr20: 61,954,156-62,031,959 CHRNA4, KCNQ2, 3 more genes
    nsv7026108copy number variation1nstd229human GRCh38 chr20: 63,313,301-63,487,200 , GRCh37.p13 chr20: 61,944,653-62,118,553 EEF1A2, LOC105372724, 7 more genes
    nsv7025717copy number variation1nstd229human GRCh38 chr20: 63,317,501-63,319,500 , GRCh37.p13 chr20: 61,948,853-61,950,852 COL20A1
    nsv7022098copy number variation1nstd229human GRCh38 chr20: 63,311,562-63,317,781 , GRCh37.p13 chr20: 61,942,914-61,949,133 COL20A1
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