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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
    nsv6137687copy number variation1nstd102humannot provided GRCh38 chr2: 36,472,472-36,866,823 , GRCh37.p13 chr2: 36,699,615-37,093,966 CRIM1, STRN, 4 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
    nsv5949820insertion1nstd209human GRCh38 chr2: 36,598,188-36,598,188 , GRCh37.p13 chr2: 36,825,331-36,825,331 FEZ2
    nsv5884367copy number variation1nstd209human GRCh38 chr2: 36,581,429-36,583,349 , GRCh37.p13 chr2: 36,808,572-36,810,492 FEZ2
    nsv5876787copy number variation1nstd209human GRCh38 chr2: 36,583,463-36,590,895 , GRCh37.p13 chr2: 36,810,606-36,818,038 FEZ2
    nsv5875883copy number variation1nstd209human GRCh38 chr2: 36,593,183-36,594,428 , GRCh37.p13 chr2: 36,820,326-36,821,571 FEZ2
    nsv5875219copy number variation1nstd209human GRCh38 chr2: 36,591,010-36,594,411 , GRCh37.p13 chr2: 36,818,153-36,821,554 FEZ2
    nsv5868005copy number variation1nstd209human GRCh38 chr2: 36,578,864-36,581,287 , GRCh37.p13 chr2: 36,806,007-36,808,430 FEZ2
    nsv5833195copy number variation1nstd209human GRCh38 chr2: 36,593,200-36,594,399 , GRCh37.p13 chr2: 36,820,343-36,821,542 FEZ2
    nsv5722219mobile element insertion1nstd211human GRCh38 chr2: 36,557,200-36,557,200 , GRCh37.p13 chr2: 36,784,343-36,784,343 FEZ2
    nsv5618223insertion1nstd207human GRCh38 chr2: 36,598,187-36,598,187 , GRCh37.p13 chr2: 36,825,330-36,825,330 FEZ2
    nsv5453495copy number variation1nstd206human GRCh38 chr2: 36,593,206-36,594,406 , GRCh37.p13 chr2: 36,820,349-36,821,549 FEZ2
    nsv5448159copy number variation1nstd206human GRCh38 chr2: 36,593,148-36,594,394 , GRCh37.p13 chr2: 36,820,291-36,821,537 FEZ2
    nsv5447865copy number variation1nstd206human GRCh38 chr2: 36,553,087-36,555,844 , GRCh37.p13 chr2: 36,780,230-36,782,987 FEZ2
    nsv5444945copy number variation1nstd206human GRCh38 chr2: 36,578,865-36,581,288 , GRCh37.p13 chr2: 36,806,008-36,808,431 FEZ2
    nsv5440150copy number variation1nstd206human GRCh38 chr2: 36,569,351-36,576,290 , GRCh37.p13 chr2: 36,796,494-36,803,433 FEZ2
    nsv5281966copy number variation1nstd204human GRCh38.p13 chr2: 36,567,709-36,569,857 , GRCh37.p13 chr2: 36,794,852-36,797,000 FEZ2
    nsv5208924copy number variation1nstd204human GRCh38.p13 chr2: 36,567,650-36,569,749 , GRCh37.p13 chr2: 36,794,793-36,796,892 FEZ2
    nsv5204987copy number variation1nstd204human GRCh38.p13 chr2: 36,592,950-36,594,499 , GRCh37.p13 chr2: 36,820,093-36,821,642 FEZ2
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