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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5890350copy number variation1nstd209human GRCh38 chr6: 35,786,783-35,799,007 , GRCh37.p13 chr6: 35,754,560-35,766,784 CLPS, CLPSL1
    nsv5844883copy number variation2nstd209human GRCh38 chr6: 35,786,777-35,797,346 , GRCh37.p13 chr6: 35,754,554-35,765,123 CLPSL1, CLPS
    nsv5633439insertion1nstd207human GRCh38 chr6: 35,794,698-35,794,698 , GRCh37.p13 chr6: 35,762,475-35,762,475 CLPS
    nsv5630578insertion1nstd207human GRCh38 chr6: 35,795,935-35,795,935 , GRCh37.p13 chr6: 35,763,712-35,763,712 CLPS
    nsv5627581insertion1nstd207human GRCh38 chr6: 35,797,677-35,797,677 , GRCh37.p13 chr6: 35,765,454-35,765,454 CLPS
    nsv5473010copy number variation1nstd206human GRCh38 chr6: 35,664,023-35,837,660 , GRCh37.p13 chr6: 35,631,800-35,805,437 CMPK1P1, CLPSL2, 8 more genes
    nsv5466563copy number variation1nstd206human GRCh38 chr6: 35,786,763-35,799,031 , GRCh37.p13 chr6: 35,754,540-35,766,808 CLPS, CLPSL1
    nsv5388979copy number variation2nstd186human GRCh37 chr6: 35,754,560-35,766,788 , GRCh38.p12 chr6: 35,786,783-35,799,011 CLPS, CLPSL1
    nsv5308174copy number variation1nstd204human GRCh38.p13 chr6: 35,786,783-35,799,011 , GRCh37.p13 chr6: 35,754,560-35,766,788 CLPS, CLPSL1
    nsv5237413copy number variation1nstd204human GRCh38.p13 chr6: 35,790,101-35,799,000 , GRCh37.p13 chr6: 35,757,878-35,766,777 CLPS, CLPSL1
    nsv5234898copy number variation1nstd204human GRCh38.p13 chr6: 35,786,477-35,798,758 , GRCh37.p13 chr6: 35,754,254-35,766,535 CLPS, CLPSL1
    nsv5230443copy number variation1nstd204human GRCh38.p13 chr6: 35,791,701-35,794,100 , GRCh37.p13 chr6: 35,759,478-35,761,877 CLPSL1, CLPS
    nsv5228700copy number variation1nstd204human GRCh38.p13 chr6: 35,786,377-35,793,507 , GRCh37.p13 chr6: 35,754,154-35,761,284 CLPSL1, CLPS
    nsv5228677copy number variation1nstd204human GRCh38.p13 chr6: 35,785,401-35,799,000 , GRCh37.p13 chr6: 35,753,178-35,766,777 CLPSL1, CLPS
    nsv5228509copy number variation1nstd204human GRCh38.p13 chr6: 35,786,801-35,802,700 , GRCh37.p13 chr6: 35,754,578-35,770,477 CLPS, CLPSL1
    nsv5223381copy number variation1nstd204human GRCh38.p13 chr6: 35,792,408-35,797,958 , GRCh37.p13 chr6: 35,760,185-35,765,735 CLPS, CLPSL1
    nsv5200371copy number variation1nstd102humanPathogenic GRCh37 chr6: 34,401,304-38,435,497 , GRCh38.p12 chr6: 34,433,527-38,467,721 RPS15AP19, FKBP5, 95 more genes
    nsv5031134inversion1nstd200human GRCh38 chr6: 35,178,266-40,407,996 , GRCh37.p13 chr6: 35,146,043-40,375,735 , LOC105375040, 114 more genes
    nsv4934626copy number variation1nstd200human GRCh38 chr6: 35,786,783-35,799,011 , GRCh37.p13 chr6: 35,754,560-35,766,788 CLPSL1, CLPS
    nsv4934622copy number variation1nstd200human GRCh38 chr6: 35,664,023-35,837,660 , GRCh37.p13 chr6: 35,631,800-35,805,437 CLPS, LOC285847, 8 more genes
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