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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5942591copy number variation1nstd209human GRCh38 chr17: 58,488,483-58,488,735 , GRCh37.p13 chr17: 56,565,844-56,566,096 MTMR4, HSF5
    nsv5941721copy number variation1nstd209human GRCh38 chr17: 58,423,419-58,423,490 , GRCh37.p13 chr17: 56,500,780-56,500,851 HSF5
    nsv5709627mobile element insertion1nstd211human GRCh38 chr17: 58,423,328-58,423,328 , GRCh37.p13 chr17: 56,500,689-56,500,689 HSF5
    nsv5597620copy number variation1nstd207human GRCh38 chr17: 58,423,419-58,423,490 , GRCh37.p13 chr17: 56,500,780-56,500,851 HSF5
    nsv5554090sequence alteration1nstd206human GRCh38 chr17: 32,109,732-67,925,723 , GRCh37.p13 chr17: 30,436,751-65,921,839 , APOH, 1099 more genes
    nsv5531812copy number variation1nstd206human GRCh38 chr17: 58,423,421-58,423,491 , GRCh37.p13 chr17: 56,500,782-56,500,852 HSF5
    nsv5527874copy number variation1nstd206human GRCh38 chr17: 58,450,328-58,453,551 , GRCh37.p13 chr17: 56,527,689-56,530,912 HSF5
    nsv5521747copy number variation1nstd206human GRCh38 chr17: 58,452,472-58,452,565 , GRCh37.p13 chr17: 56,529,833-56,529,926 HSF5
    nsv5520038copy number variation1nstd206human GRCh38 chr17: 58,424,567-58,425,553 , GRCh37.p13 chr17: 56,501,928-56,502,914 HSF5
    nsv5514753copy number variation1nstd206human GRCh38 chr17: 58,450,908-58,453,827 , GRCh37.p13 chr17: 56,528,269-56,531,188 HSF5
    nsv5381036copy number variation1nstd102humanUncertain significance GRCh37 chr17: 56,432,304-56,811,583 , GRCh38.p12 chr17: 58,354,943-58,734,222 SEPTIN4-AS1, MTMR4, 13 more genes
    nsv5358995translocation1nstd200human GRCh38 chr17: 58,453,551-58,453,551 , GRCh38 chr17: 58,450,325-58,450,325 , GRCh37.p13 chr17: 56,527,686-56,527,686 , GRCh37.p13 chr17: 56,530,912-56,530,912 HSF5
    nsv5338134translocation1nstd200human GRCh37 chr17: 56,500,782-56,500,782 , GRCh37 chr17: 56,500,852-56,500,852 , GRCh38.p12 chr17: 58,423,421-58,423,421 , GRCh38.p12 chr17: 58,423,491-58,423,491 HSF5
    nsv5323679copy number variation1nstd204human GRCh38.p13 chr17: 58,450,831-58,457,481 , GRCh37.p13 chr17: 56,528,192-56,534,842 HSF5
    nsv5289195copy number variation1nstd204human GRCh38.p13 chr17: 58,450,839-58,457,279 , GRCh37.p13 chr17: 56,528,200-56,534,640 HSF5
    nsv5150850mobile element insertion1nstd203human GRCh38 chr17: 58,430,040-58,430,056 , GRCh37.p13 chr17: 56,507,401-56,507,417 HSF5
    nsv5013852copy number variation1nstd200human GRCh38 chr17: 58,424,549-58,425,617 , GRCh37.p13 chr17: 56,501,910-56,502,978 HSF5
    nsv5010367copy number variation1nstd200human GRCh38 chr17: 58,474,354-58,479,612 , GRCh37.p13 chr17: 56,551,715-56,556,973 HSF5, SETP3
    nsv4851468copy number variation1nstd200human GRCh37 chr17: 56,551,715-56,556,973 , GRCh38.p12 chr17: 58,474,354-58,479,612 HSF5, SETP3
    nsv4671063copy number variation1nstd186human GRCh37 chr17: 56,527,656-56,530,912 , GRCh38.p12 chr17: 58,450,295-58,453,551 HSF5
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