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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5945678copy number variation1nstd209human GRCh38 chr17: 39,428,039-39,428,155 , GRCh37.p13 chr17: 37,584,292-37,584,408 MED1
    nsv5936219copy number variation1nstd209human GRCh38 chr17: 39,421,207-39,421,505 , GRCh37.p13 chr17: 37,577,460-37,577,758 MED1
    nsv5931895copy number variation1nstd209human GRCh38 chr17: 39,430,414-39,430,739 , GRCh37.p13 chr17: 37,586,667-37,586,992 MED1
    nsv5700384mobile element insertion1nstd211human GRCh38 chr17: 39,443,812-39,443,812 , GRCh37.p13 chr17: 37,600,065-37,600,065 MED1
    nsv5700250mobile element insertion1nstd211human GRCh38 chr17: 39,414,665-39,414,665 , GRCh37.p13 chr17: 37,570,918-37,570,918 MED1
    nsv5554090sequence alteration1nstd206human GRCh38 chr17: 32,109,732-67,925,723 , GRCh37.p13 chr17: 30,436,751-65,921,839 , APOH, 1099 more genes
    nsv5533906copy number variation1nstd206human GRCh38 chr17: 39,441,838-39,442,358 , GRCh37.p13 chr17: 37,598,091-37,598,611 MED1
    nsv5526551copy number variation1nstd206human GRCh38 chr17: 39,428,039-39,428,156 , GRCh37.p13 chr17: 37,584,292-37,584,409 MED1
    nsv5520886copy number variation1nstd206human GRCh38 chr17: 39,411,798-39,412,816 , GRCh37.p13 chr17: 37,568,051-37,569,069 MED1
    nsv5358852translocation1nstd200human GRCh38 chr17: 39,411,798-39,411,798 , GRCh38 chr17: 39,412,816-39,412,816 , GRCh37.p13 chr17: 37,568,051-37,568,051 , GRCh37.p13 chr17: 37,569,069-37,569,069 MED1
    nsv5320424copy number variation1nstd204human GRCh38.p13 chr17: 39,411,768-39,412,845 , GRCh37.p13 chr17: 37,568,021-37,569,098 MED1
    nsv5282343copy number variation1nstd204human GRCh38.p13 chr17: 39,365,001-39,413,900 , GRCh37.p13 chr17: 37,521,254-37,570,153 MED1, FBXL20
    nsv5281205copy number variation1nstd204human GRCh38.p13 chr17: 39,355,201-39,495,300 , GRCh37.p13 chr17: 37,511,454-37,651,553 MED1, CDK12, 1 more genes
    nsv5280924copy number variation1nstd204human GRCh38.p13 chr17: 39,129,801-39,494,000 , GRCh37.p13 chr17: 37,286,054-37,650,253 RPL19, TRC-GCA2-4, 11 more genes
    nsv5159504mobile element insertion1nstd203human GRCh38 chr17: 39,414,643-39,414,665 , GRCh37.p13 chr17: 37,570,896-37,570,918 MED1
    nsv5152382mobile element insertion1nstd203human GRCh38 chr17: 39,414,652-39,414,656 , GRCh37.p13 chr17: 37,570,905-37,570,909 MED1
    nsv5029106copy number variation1nstd200human GRCh38 chr17: 39,420,955-39,422,474 , GRCh37.p13 chr17: 37,577,208-37,578,727 MED1
    nsv5029104copy number variation1nstd200human GRCh38 chr17: 39,380,352-39,426,046 , GRCh37.p13 chr17: 37,536,605-37,582,299 MED1, FBXL20
    nsv5029102copy number variation1nstd200human GRCh38 chr17: 39,346,233-39,442,478 , GRCh37.p13 chr17: 37,502,486-37,598,731 FBXL20, MED1
    nsv5016292copy number variation1nstd200human GRCh38 chr17: 39,436,164-39,438,157 , GRCh37.p13 chr17: 37,592,417-37,594,410 MED1
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