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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5969474insertion1nstd209human GRCh38 chr20: 30,406,411-30,406,411 , GRCh37.p13 chr20: 29,641,087-29,641,087 FRG1BP
    nsv5966877copy number variation1nstd209human GRCh38 chr20: 29,125,619-30,424,446 , GRCh37.p13 chr20: 25,864,401-29,615,130 DUX4L33, LOC105379476, 27 more genes
    nsv5965062copy number variation1nstd209human GRCh38 chr20: 29,285,033-30,468,916 , GRCh37.p13 chr4: 190,198,664-190,843,361 , GRCh37.p13 chr20: 25,864,401-29,615,130 LOC110467538, RNA5SP532, 27 more genes
    nsv5960957copy number variation1nstd209human GRCh38 chr20: 30,412,861-30,413,025 , GRCh37.p13 chr20: 29,647,537-29,647,701 FRG1BP
    nsv5954916copy number variation1nstd209human GRCh38 chr20: 29,108,114-30,407,063 , GRCh37.p13 chr20: 25,864,401-29,615,130 , GRCh37.p13 chr9: 66,459,367-68,422,752 LOC110467522, LOC105379476, 27 more genes
    nsv5886964copy number variation2nstd209human GRCh38 chr20: 30,386,369-30,389,137 , GRCh37.p13 chr20: 29,621,045-29,623,813 FRG1BP
    nsv5884582copy number variation2nstd209human GRCh38 chr20: 30,381,988-30,384,131 , GRCh37.p13 chr20: 29,616,664-29,618,807 FRG1BP
    nsv5882459copy number variation2nstd209human GRCh38 chr20: 30,400,818-30,403,787 , GRCh37.p13 chr20: 29,635,494-29,638,463 FRG1BP, MLLT10P1
    nsv5880889copy number variation1nstd209human GRCh38 chr20: 30,377,639-30,383,222 , GRCh37.p13 chr20: 29,612,315-29,617,898 FRG1BP
    nsv5880471copy number variation1nstd209human GRCh38 chr20: 30,407,495-30,410,625 , GRCh37.p13 chr20: 29,642,171-29,645,301 FRG1BP
    nsv5877270copy number variation2nstd209human GRCh38 chr20: 30,393,941-30,396,294 , GRCh37.p13 chr20: 29,628,617-29,630,970 FRG1BP
    nsv5715338mobile element insertion1nstd211human GRCh38 chr20: 30,403,911-30,403,911 , GRCh37.p13 chr20: 29,638,587-29,638,587 FRG1BP, MLLT10P1
    nsv5526658copy number variation1nstd206human GRCh38 chr20: 30,400,701-30,402,442 , GRCh37.p13 chr20: 29,635,377-29,637,118 FRG1BP, MLLT10P1
    nsv5514026copy number variation1nstd206human GRCh38 chr20: 30,404,925-30,405,782 , GRCh37.p13 chr20: 29,639,601-29,640,458 FRG1BP
    nsv5366069translocation1nstd200human GRCh38 chr20: 30,377,207-30,377,207 , GRCh38 chr22: 36,160,825-36,160,825 , GRCh37.p13 chr20: 29,611,883-29,611,883 , GRCh37.p13 chr22: 36,556,873-36,556,873 APOL3, FRG1BP
    nsv5337377translocation1nstd200human GRCh37 chr20: 29,653,908-29,653,908 , GRCh37 chrUn|GL000219.1: 57,127-57,127 , GRCh38.p9 chrUn|GL000219.1: 57,127-57,127 , GRCh38.p9 chrUn|GL000219.1: 57,127-57,127 , GRCh38.p12 chr20: 30,419,232-30,419,232 FRG1BP
    nsv5333096translocation1nstd200human GRCh37 chr4: 190,200,698-190,200,698 , GRCh37 chr20: 29,653,908-29,653,908 , GRCh38.p12 chr20: 30,419,232-30,419,232 , GRCh38.p12 chr4: 189,279,544-189,279,544 FRG1BP
    nsv5300047copy number variation1nstd204human GRCh38.p13 chr20: 30,377,816-30,383,397 , GRCh37.p13 chr20: 29,612,492-29,618,073 FRG1BP
    nsv5299439copy number variation1nstd204human GRCh38.p13 chr20: 30,395,346-30,401,467 , GRCh37.p13 chr20: 29,630,022-29,636,143 MLLT10P1, FRG1BP
    nsv5299343copy number variation1nstd204human GRCh38.p13 chr20: 30,417,516-30,420,045 , GRCh37.p13 chr20: 29,652,192-29,653,908 FRG1BP
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