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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
    nsv5966011insertion1nstd209human GRCh38 chr2: 37,965,881-37,965,881 , GRCh37.p13 chr2: 38,193,024-38,193,024 RMDN2-AS1, RMDN2
    nsv5886507copy number variation1nstd209human GRCh38 chr2: 37,963,434-37,976,923 , GRCh37.p13 chr2: 38,190,577-38,204,066 RMDN2-AS1, RMDN2
    nsv5879902copy number variation1nstd209human GRCh38 chr2: 37,958,335-37,959,976 , GRCh37.p13 chr2: 38,185,478-38,187,119 RMDN2-AS1, RMDN2
    nsv5873466copy number variation1nstd209human GRCh38 chr2: 37,970,268-37,970,656 , GRCh37.p13 chr2: 38,197,411-38,197,799 RMDN2-AS1, RMDN2
    nsv5833203copy number variation1nstd209human GRCh38 chr2: 37,965,542-37,974,277 , GRCh37.p13 chr2: 38,192,685-38,201,420 RMDN2-AS1, RMDN2
    nsv5832895copy number variation2nstd209human GRCh38 chr2: 37,958,321-37,959,943 , GRCh37.p13 chr2: 38,185,464-38,187,086 RMDN2, RMDN2-AS1
    nsv5832638copy number variation1nstd209human GRCh38 chr2: 38,030,935-38,034,178 , GRCh37.p13 chr2: 38,258,078-38,261,321 RMDN2-AS1, RMDN2
    nsv5691687mobile element insertion1nstd211human GRCh38 chr2: 38,052,197-38,052,197 , GRCh37.p13 chr2: 38,279,340-38,279,340 RMDN2
    nsv5686009mobile element insertion1nstd211human GRCh38 chr2: 37,965,893-37,965,893 , GRCh37.p13 chr2: 38,193,036-38,193,036 RMDN2-AS1, RMDN2
    nsv5683044mobile element insertion1nstd211human GRCh38 chr2: 38,018,760-38,018,760 , GRCh37.p13 chr2: 38,245,903-38,245,903 RMDN2-AS1, RMDN2
    nsv5680943mobile element insertion2nstd211human GRCh38 chr2: 37,991,904-37,991,904 , GRCh37.p13 chr2: 38,219,047-38,219,047 RMDN2, RMDN2-AS1
    nsv5677270mobile element insertion2nstd211human GRCh38 chr2: 37,942,379-37,942,379 , GRCh37.p13 chr2: 38,169,522-38,169,522 RMDN2
    nsv5577608copy number variation1nstd207human GRCh38 chr2: 37,958,335-37,959,976 , GRCh37.p13 chr2: 38,185,478-38,187,119 RMDN2-AS1, RMDN2
    nsv5546002insertion1nstd206human GRCh38 chr2: 38,052,361-38,052,404 , GRCh37.p13 chr2: 38,279,504-38,279,547 RMDN2
    nsv5450513copy number variation1nstd206human GRCh38 chr2: 37,958,341-37,959,977 , GRCh37.p13 chr2: 38,185,484-38,187,120 RMDN2, RMDN2-AS1
    nsv5449689copy number variation1nstd206human GRCh38 chr2: 37,970,271-37,970,657 , GRCh37.p13 chr2: 38,197,414-38,197,800 RMDN2, RMDN2-AS1
    nsv5410402mobile element insertion1nstd206human GRCh38 chr2: 38,052,197-38,052,248 , GRCh37.p13 chr2: 38,279,340-38,279,391 RMDN2
    nsv5402816mobile element insertion1nstd206human GRCh38 chr2: 37,991,904-37,991,955 , GRCh37.p13 chr2: 38,219,047-38,219,098 RMDN2, RMDN2-AS1
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