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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5925437copy number variation1nstd209human GRCh38 chr9: 128,511,854-128,512,212 , GRCh37.p13 chr9: 131,274,133-131,274,491 GLE1
    nsv5855739copy number variation1nstd209human GRCh38 chr9: 128,525,219-128,527,644 , GRCh37.p13 chr9: 131,287,498-131,289,923 LOC101929270, GLE1
    nsv5851825copy number variation1nstd209human GRCh38 chr9: 128,528,895-128,530,429 , GRCh37.p13 chr9: 131,291,174-131,292,708 GLE1, LOC101929270
    nsv5720239mobile element insertion1nstd211human GRCh38 chr9: 128,541,324-128,541,324 , GRCh37.p13 chr9: 131,303,603-131,303,603 GLE1, LOC101929270
    nsv5674065copy number variation1nstd102humanPathogenic GRCh37 chr9: 131,295,782-131,296,240 , GRCh38.p12 chr9: 128,533,503-128,533,961 GLE1, LOC101929270
    nsv5559459mobile element insertion1nstd206human GRCh38 chr9: 128,541,324-128,541,375 , GRCh37.p13 chr9: 131,303,603-131,303,654 GLE1, LOC101929270
    nsv5493898copy number variation1nstd206human GRCh38 chr9: 128,511,855-128,512,213 , GRCh37.p13 chr9: 131,274,134-131,274,492 GLE1
    nsv5241889copy number variation1nstd204human GRCh38.p13 chr9: 128,441,101-129,240,100 , GRCh37.p13 chr9: 131,203,380-132,002,379 , KYAT1, 32 more genes
    nsv5138128mobile element insertion1nstd203human GRCh38 chr9: 128,534,868-128,534,898 , GRCh37.p13 chr9: 131,297,147-131,297,177 LOC101929270, GLE1
    nsv4988395copy number variation1nstd200human GRCh38 chr9: 128,498,819-128,507,773 , GRCh37.p13 chr9: 131,261,098-131,270,052 ODF2, GLE1
    nsv4988394copy number variation1nstd200human GRCh38 chr9: 128,498,445-128,502,928 , GRCh37.p13 chr9: 131,260,724-131,265,207 ODF2, GLE1
    nsv4985740copy number variation1nstd200human GRCh38 chr9: 128,105,845-128,709,294 , GRCh37.p13 chr9: 130,868,124-131,471,573 , SET, 33 more genes
    nsv4840895copy number variation1nstd200human GRCh37 chr9: 131,261,098-131,270,052 , GRCh38.p12 chr9: 128,498,819-128,507,773 GLE1, ODF2
    nsv4837188copy number variation1nstd200human GRCh37 chr9: 131,274,134-131,274,492 , GRCh38.p12 chr9: 128,511,855-128,512,213 GLE1
    nsv4834491copy number variation1nstd200human GRCh37 chr9: 131,260,724-131,265,207 , GRCh38.p12 chr9: 128,498,445-128,502,928 ODF2, GLE1
    nsv4769385copy number variation1nstd102humanUncertain significance GRCh37 chr9: 131,282,528-131,720,659 , GRCh38.p12 chr9: 128,520,249-128,958,380 LOC101929270, TBC1D13, 20 more genes
    nsv4768374copy number variation1nstd102humanPathogenic GRCh37 chr9: 130,412,438-131,423,964 , GRCh38.p12 chr9: 127,650,159-128,661,685 COQ4, GLE1, 53 more genes
    nsv4683557copy number variation1nstd102humanPathogenic GRCh37 chr9: 130,577,951-131,303,459 , GRCh38.p12 chr9: 127,815,672-128,541,180 SWI5, LOC105379841, 36 more genes
    nsv4682627copy number variation1nstd102humanLikely pathogenic GRCh37 chr9: 131,300,255-131,303,459 , GRCh38.p12 chr9: 128,537,976-128,541,180 GLE1, LOC101929270
    nsv4682206copy number variation1nstd102humanPathogenic GRCh37 chr9: 131,284,937-131,289,814 , GRCh38.p12 chr9: 128,522,658-128,527,535 LOC101929270, GLE1
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