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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5973007insertion1nstd209human GRCh38 chr18: 12,332,949-12,332,949 , GRCh37.p13 chr18: 12,332,948-12,332,948 AFG3L2
    nsv5672896copy number variation1nstd102humanPathogenic GRCh37 chr18: 2,656,075-13,885,536 , GRCh38.p12 chr18: 2,656,076-13,885,537 RN7SL862P, LOC105371972, 181 more genes
    nsv5653696insertion1nstd207human GRCh38 chr18: 12,362,724-12,362,724 , GRCh37.p13 chr18: 12,362,723-12,362,723 AFG3L2
    nsv5526676copy number variation1nstd206human GRCh38 chr18: 12,364,094-12,364,649 , GRCh37.p13 chr18: 12,364,093-12,364,648 AFG3L2
    nsv5518148copy number variation1nstd206human GRCh38 chr18: 12,339,493-12,339,790 , GRCh37.p13 chr18: 12,339,492-12,339,789 LOC107985154, AFG3L2
    nsv5375100translocation1nstd200human GRCh38 chr18: 12,326,903-12,326,903 , GRCh38 chr18: 12,328,583-12,328,583 , GRCh37.p13 chr18: 12,326,902-12,326,902 , GRCh37.p13 chr18: 12,328,582-12,328,582 TUBB6, AFG3L2
    nsv5349879translocation1nstd200human GRCh38 chr18: 12,332,550-12,332,550 , GRCh38 chr18: 12,332,468-12,332,468 , GRCh37.p13 chr18: 12,332,467-12,332,467 , GRCh37.p13 chr18: 12,332,549-12,332,549 AFG3L2
    nsv5349878translocation1nstd200human GRCh38 chr18: 12,329,785-12,329,785 , GRCh38 chr18: 12,337,338-12,337,338 , GRCh37.p13 chr18: 12,329,784-12,329,784 , GRCh37.p13 chr18: 12,337,337-12,337,337 AFG3L2, TUBB6, 1 more genes
    nsv5341819translocation1nstd200human GRCh37 chr18: 12,339,777-12,339,777 , GRCh37 chr18: 12,339,529-12,339,529 , GRCh38.p12 chr18: 12,339,778-12,339,778 , GRCh38.p12 chr18: 12,339,530-12,339,530 AFG3L2, LOC107985154
    nsv5332920translocation1nstd200human GRCh37 chr18: 12,328,582-12,328,582 , GRCh37 chr18: 12,326,902-12,326,902 , GRCh38.p12 chr18: 12,326,903-12,326,903 , GRCh38.p12 chr18: 12,328,583-12,328,583 AFG3L2, TUBB6
    nsv5146907mobile element insertion1nstd203human GRCh38 chr18: 12,343,729-12,343,745 , GRCh37.p13 chr18: 12,343,728-12,343,744 LOC107985154, AFG3L2
    nsv5026666copy number variation1nstd200human GRCh38 chr18: 12,045,885-12,921,903 , GRCh37.p13 chr18: 12,045,884-12,921,902 PTPN2, MIX23P3, 25 more genes
    nsv5017707copy number variation1nstd200human GRCh38 chr18: 12,377,304-12,377,379 , GRCh37.p13 chr18: 12,377,303-12,377,378 AFG3L2
    nsv5014290copy number variation1nstd200human GRCh38 chr18: 12,340,828-12,422,067 , GRCh37.p13 chr18: 12,340,827-12,422,066 RNU7-129P, AFG3L2, 2 more genes
    nsv4854550copy number variation1nstd200human GRCh37 chr18: 12,340,827-12,422,066 , GRCh38.p12 chr18: 12,340,828-12,422,067 PRELID3A, LOC107985154, 2 more genes
    nsv4852120copy number variation1nstd200human GRCh37 chr18: 12,361,235-12,361,477 , GRCh38.p12 chr18: 12,361,236-12,361,478 AFG3L2
    nsv4852119copy number variation1nstd200human GRCh37 chr18: 12,344,532-12,346,719 , GRCh38.p12 chr18: 12,344,533-12,346,720 AFG3L2, LOC107985154
    nsv4729915copy number variation1nstd102humanPathogenic GRCh37 chr18: 7,598,173-15,422,644 , GRCh38.p12 chr18: 7,598,175-15,410,899 CEP192, RNU2-27P, 155 more genes
    nsv4703193copy number variation1nstd195human GRCh37 chr18: 12,356,134-12,356,135 , GRCh38.p12 chr18: 12,356,135-12,356,136 AFG3L2
    nsv4684337copy number variation1nstd102humanLikely pathogenic GRCh37 chr18: 12,362,219-12,423,408 , GRCh38.p12 chr18: 12,362,220-12,423,409 PRELID3A, AFG3L2, 1 more genes
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