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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112661copy number variation1nstd102humanPathogenic GRCh37 chr1: 231,407,943-237,289,859 , GRCh38.p12 chr1: 231,272,197-237,126,559 LOC105373207, LOC105373210, 113 more genes
    nsv5950724insertion1nstd209human GRCh38 chr1: 236,239,807-236,239,807 , GRCh37.p13 chr1: 236,403,107-236,403,107 ERO1B
    nsv5870168copy number variation1nstd209human GRCh38 chr1: 236,263,075-236,265,328 , GRCh37.p13 chr1: 236,426,375-236,428,628 ERO1B
    nsv5869773copy number variation1nstd209human GRCh38 chr1: 236,267,333-236,267,457 , GRCh37.p13 chr1: 236,430,633-236,430,757 RNU2-70P, ERO1B
    nsv5868952copy number variation1nstd209human GRCh38 chr1: 236,271,688-236,272,653 , GRCh37.p13 chr1: 236,434,988-236,435,953 ERO1B
    nsv5829556copy number variation2nstd209human GRCh38 chr1: 236,263,034-236,265,960 , GRCh37.p13 chr1: 236,426,334-236,429,260 RNU2-70P, ERO1B
    nsv5829495copy number variation1nstd209human GRCh38 chr1: 236,248,994-236,263,383 , GRCh37.p13 chr1: 236,412,294-236,426,683 ERO1B
    nsv5693090mobile element insertion1nstd211human GRCh38 chr1: 236,263,806-236,263,806 , GRCh37.p13 chr1: 236,427,106-236,427,106 ERO1B
    nsv5692787mobile element insertion1nstd211human GRCh38 chr1: 236,255,741-236,255,741 , GRCh37.p13 chr1: 236,419,041-236,419,041 ERO1B
    nsv5686550mobile element insertion1nstd211human GRCh38 chr1: 236,265,293-236,265,293 , GRCh37.p13 chr1: 236,428,593-236,428,593 ERO1B
    nsv5684631mobile element insertion1nstd211human GRCh38 chr1: 236,261,963-236,261,963 , GRCh37.p13 chr1: 236,425,263-236,425,263 ERO1B
    nsv5683048mobile element insertion1nstd211human GRCh38 chr1: 236,261,941-236,261,941 , GRCh37.p13 chr1: 236,425,241-236,425,241 ERO1B
    nsv5678669mobile element insertion1nstd211human GRCh38 chr1: 236,238,209-236,238,209 , GRCh37.p13 chr1: 236,401,509-236,401,509 ERO1B
    nsv5620266insertion1nstd207human GRCh38 chr1: 236,245,314-236,245,314 , GRCh37.p13 chr1: 236,408,614-236,408,614 ERO1B
    nsv5615365insertion1nstd207human GRCh38 chr1: 236,245,498-236,245,498 , GRCh37.p13 chr1: 236,408,798-236,408,798 ERO1B
    nsv5608983insertion1nstd207human GRCh38 chr1: 236,239,861-236,239,861 , GRCh37.p13 chr1: 236,403,161-236,403,161 ERO1B
    nsv5583580copy number variation1nstd207human GRCh38 chr1: 236,245,296-236,245,523 , GRCh37.p13 chr1: 236,408,596-236,408,823 ERO1B
    nsv5579595copy number variation1nstd207human GRCh38 chr1: 236,245,472-236,245,525 , GRCh37.p13 chr1: 236,408,772-236,408,825 ERO1B
    nsv5573328copy number variation1nstd207human GRCh38 chr1: 236,245,416-236,245,525 , GRCh37.p13 chr1: 236,408,716-236,408,825 ERO1B
    nsv5446793copy number variation1nstd206human GRCh38 chr1: 236,271,657-236,272,654 , GRCh37.p13 chr1: 236,434,957-236,435,954 ERO1B
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