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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6137788copy number variation1nstd102humanPathogenic GRCh37 chr2: 24,601,818-43,466,284 , GRCh38.p12 chr2: 24,378,949-43,239,145 GTF3C2-AS1, MAPRE3-AS1, 316 more genes
    nsv6112680copy number variation1nstd102humanLikely pathogenic GRCh37 chr2: 24,881,528-43,460,021 , GRCh38.p12 chr2: 24,658,659-43,232,882 ADCY3, ALK, 314 more genes
    nsv5964242insertion1nstd209human GRCh38 chr2: 31,966,732-31,966,732 , GRCh37.p13 chr2: 32,191,801-32,191,801 MEMO1
    nsv5887228copy number variation1nstd209human GRCh38 chr2: 31,976,305-31,978,113 , GRCh37.p13 chr2: 32,201,374-32,203,182 MEMO1
    nsv5885884copy number variation1nstd209human GRCh38 chr2: 31,985,822-31,985,889 , GRCh37.p13 chr2: 32,210,891-32,210,958 MEMO1
    nsv5881576copy number variation1nstd209human GRCh38 chr2: 31,743,142-31,898,199 , GRCh37.p13 chr2: 31,968,211-32,123,268 MEMO1, AK2P2, 3 more genes
    nsv5875264copy number variation1nstd209human GRCh38 chr2: 31,982,023-31,982,315 , GRCh37.p13 chr2: 32,207,092-32,207,384 MEMO1
    nsv5872662copy number variation1nstd209human GRCh38 chr2: 31,901,759-31,901,930 , GRCh37.p13 chr2: 32,126,828-32,126,999 MEMO1
    nsv5689591mobile element insertion2nstd211human GRCh38 chr2: 31,941,760-31,941,760 , GRCh37.p13 chr2: 32,166,829-32,166,829 MEMO1
    nsv5686056mobile element insertion1nstd211human GRCh38 chr2: 31,992,064-31,992,064 , GRCh37.p13 chr2: 32,217,133-32,217,133 MEMO1
    nsv5685503mobile element insertion1nstd211human GRCh38 chr2: 31,968,846-31,968,846 , GRCh37.p13 chr2: 32,193,915-32,193,915 MEMO1
    nsv5569797copy number variation1nstd207human GRCh38 chr2: 31,901,759-31,901,930 , GRCh37.p13 chr2: 32,126,828-32,126,999 MEMO1
    nsv5538754insertion1nstd206human GRCh38 chr2: 32,002,239-32,002,289 , GRCh37.p13 chr2: 32,227,308-32,227,358 MEMO1
    nsv5452390copy number variation1nstd206human GRCh38 chr2: 31,901,760-31,901,931 , GRCh37.p13 chr2: 32,126,829-32,127,000 MEMO1
    nsv5450583copy number variation1nstd206human GRCh38 chr2: 31,960,019-31,971,616 , GRCh37.p13 chr2: 32,185,088-32,196,685 MEMO1
    nsv5446406copy number variation1nstd206human GRCh38 chr2: 31,896,829-31,897,242 , GRCh37.p13 chr2: 32,121,898-32,122,311 MEMO1
    nsv5443640copy number variation1nstd206human GRCh38 chr2: 31,985,822-31,985,892 , GRCh37.p13 chr2: 32,210,891-32,210,961 MEMO1
    nsv5442111copy number variation1nstd206human GRCh38 chr2: 31,953,465-31,959,602 , GRCh37.p13 chr2: 32,178,534-32,184,671 MEMO1
    nsv5434790copy number variation1nstd206human GRCh38 chr2: 31,976,333-31,978,103 , GRCh37.p13 chr2: 32,201,402-32,203,172 MEMO1
    nsv5408449mobile element insertion1nstd206human GRCh38 chr2: 31,941,760-31,941,811 , GRCh37.p13 chr2: 32,166,829-32,166,880 MEMO1
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