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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6137705copy number variation1nstd102humanPathogenic GRCh37 chr9: 36,419,493-40,774,118 , GRCh38.p12 chr9: 61,281,967-67,217,006 , GRCh38.p12 chr9: 36,419,496-39,445,729 ZNF658B, LOC105379814, 208 more genes
    nsv6137704copy number variation1nstd102humanPathogenic GRCh37 chr9: 36,426,622-38,787,479 , GRCh38.p12 chr9: 36,426,625-38,787,482 MELK, SLC25A51, 55 more genes
    nsv6137702copy number variation1nstd102humanPathogenic GRCh37 chr9: 35,059,633-37,660,586 , GRCh38.p12 chr9: 35,059,636-37,660,589 ARHGEF39, LOC105376026, 84 more genes
    nsv6137700copy number variation1nstd102humanPathogenic GRCh37 chr9: 36,088,563-39,092,820 , GRCh38.p12 chr9: 36,088,566-39,092,823 SNX18P3, VN1R48P, 69 more genes
    nsv5972210inversion1nstd209human GRCh38 chr9: 36,238,245-37,822,315 , GRCh37.p13 chr9: 36,238,242-37,822,312 PAX5, GRHPR, 35 more genes
    nsv5953944insertion1nstd209human GRCh38 chr9: 37,521,332-37,521,332 , GRCh37.p13 chr9: 37,521,329-37,521,329 FBXO10
    nsv5926618copy number variation1nstd209human GRCh38 chr9: 37,517,505-37,517,564 , GRCh37.p13 chr9: 37,517,502-37,517,561 FBXO10
    nsv5925815copy number variation1nstd209human GRCh38 chr9: 37,502,510-37,515,062 , GRCh37.p13 chr9: 37,502,507-37,515,059 POLR1E, FBXO10
    nsv5915014copy number variation1nstd209human GRCh38 chr9: 37,575,725-37,575,774 , GRCh37.p13 chr9: 37,575,722-37,575,771 FBXO10
    nsv5863489copy number variation1nstd209human GRCh38 chr9: 37,507,432-37,514,931 , GRCh37.p13 chr9: 37,507,429-37,514,928 FBXO10
    nsv5862237copy number variation1nstd209human GRCh38 chr9: 37,503,332-37,510,331 , GRCh37.p13 chr9: 37,503,329-37,510,328 FBXO10, POLR1E
    nsv5642753insertion1nstd207human GRCh38 chr9: 37,517,505-37,517,505 , GRCh37.p13 chr9: 37,517,502-37,517,502 FBXO10
    nsv5592546copy number variation1nstd207human GRCh38 chr9: 37,575,725-37,575,774 , GRCh37.p13 chr9: 37,575,722-37,575,771 FBXO10
    nsv5488072copy number variation1nstd206human GRCh38 chr9: 37,502,510-37,515,064 , GRCh37.p13 chr9: 37,502,507-37,515,061 POLR1E, FBXO10
    nsv5484121copy number variation1nstd206human GRCh38 chr9: 37,576,153-37,576,323 , GRCh37.p13 chr9: 37,576,150-37,576,320 FBXO10
    nsv5481408copy number variation1nstd206human GRCh38 chr9: 37,521,268-37,521,379 , GRCh37.p13 chr9: 37,521,265-37,521,376 FBXO10
    nsv5373619translocation1nstd200human GRCh38 chr1: 212,939,350-212,939,350 , GRCh38 chr9: 37,569,092-37,569,092 , GRCh37.p13 chr9: 37,569,089-37,569,089 , GRCh37.p13 chr1: 213,112,692-213,112,692 FBXO10
    nsv5355146translocation1nstd200human GRCh38 chr1: 212,940,624-212,940,624 , GRCh38 chr9: 37,569,078-37,569,078 , GRCh37.p13 chr1: 213,113,966-213,113,966 , GRCh37.p13 chr9: 37,569,075-37,569,075 FBXO10
    nsv5339288translocation1nstd200human GRCh37 chr9: 37,515,061-37,515,061 , GRCh37 chr9: 37,502,507-37,502,507 , GRCh38.p12 chr9: 37,502,510-37,502,510 , GRCh38.p12 chr9: 37,515,064-37,515,064 POLR1E, FBXO10
    nsv5305121copy number variation1nstd204human GRCh38.p13 chr9: 37,502,500-37,515,066 , GRCh37.p13 chr9: 37,502,497-37,515,063 FBXO10, POLR1E
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