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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
    nsv5885697copy number variation1nstd209human GRCh38 chr2: 36,444,756-36,444,839 , GRCh37.p13 chr2: 36,671,899-36,671,982 CRIM1
    nsv5885197copy number variation1nstd209human GRCh38 chr2: 36,390,430-36,392,088 , GRCh37.p13 chr2: 36,617,573-36,619,231 CRIM1
    nsv5877814copy number variation1nstd209human GRCh38 chr2: 36,549,248-36,549,536 , GRCh37.p13 chr2: 36,776,391-36,776,679 CRIM1
    nsv5877058copy number variation1nstd209human GRCh38 chr2: 36,480,529-36,482,375 , GRCh37.p13 chr2: 36,707,672-36,709,518 CRIM1
    nsv5832884copy number variation1nstd209human GRCh38 chr2: 36,480,508-36,482,407 , GRCh37.p13 chr2: 36,707,651-36,709,550 CRIM1
    nsv5721764mobile element insertion2nstd211human GRCh38 chr2: 36,392,572-36,392,572 , GRCh37.p13 chr2: 36,619,715-36,619,715 CRIM1
    nsv5689675mobile element insertion1nstd211human GRCh38 chr2: 36,433,772-36,433,772 , GRCh37.p13 chr2: 36,660,915-36,660,915 CRIM1
    nsv5684067mobile element insertion1nstd211human GRCh38 chr2: 36,524,453-36,524,453 , GRCh37.p13 chr2: 36,751,596-36,751,596 CRIM1
    nsv5679985mobile element insertion1nstd211human GRCh38 chr2: 36,392,460-36,392,460 , GRCh37.p13 chr2: 36,619,603-36,619,603 CRIM1
    nsv5675535mobile element insertion1nstd211human GRCh38 chr2: 36,447,724-36,447,724 , GRCh37.p13 chr2: 36,674,867-36,674,867 CRIM1
    nsv5611256insertion1nstd207human GRCh38 chr2: 36,447,710-36,447,710 , GRCh37.p13 chr2: 36,674,853-36,674,853 CRIM1
    nsv5609466insertion1nstd207human GRCh38 chr2: 36,505,307-36,505,307 , GRCh37.p13 chr2: 36,732,450-36,732,450 CRIM1
    nsv5583031copy number variation1nstd207human GRCh38 chr2: 36,505,307-36,505,560 , GRCh37.p13 chr2: 36,732,450-36,732,703 CRIM1
    nsv5450223copy number variation1nstd206human GRCh38 chr2: 36,455,088-36,461,289 , GRCh37.p13 chr2: 36,682,231-36,688,432 CRIM1
    nsv5442673copy number variation1nstd206human GRCh38 chr2: 36,451,517-36,451,663 , GRCh37.p13 chr2: 36,678,660-36,678,806 CRIM1
    nsv5441029copy number variation1nstd206human GRCh38 chr2: 36,373,902-36,375,553 , GRCh37.p13 chr2: 36,601,045-36,602,696 CRIM1
    nsv5434081copy number variation1nstd206human GRCh38 chr2: 36,498,638-36,498,866 , GRCh37.p13 chr2: 36,725,781-36,726,009 CRIM1
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