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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6130746insertion1nstd186human GRCh37 chr17: 41,119,603-41,119,605 , GRCh38.p12 chr17: 42,967,586-42,967,588 PTGES3L, PTGES3L-AARSD1
    nsv5978268insertion1nstd209human GRCh38 chr17: 42,967,537-42,967,537 , GRCh37.p13 chr17: 41,119,554-41,119,554 PTGES3L-AARSD1, PTGES3L
    nsv5944188copy number variation1nstd209human GRCh38 chr17: 42,975,750-42,976,055 , GRCh37.p13 chr17: 41,127,767-41,128,072 PTGES3L, PTGES3L-AARSD1
    nsv5940129copy number variation1nstd209human GRCh38 chr17: 42,970,801-42,971,095 , GRCh37.p13 chr17: 41,122,818-41,123,112 PTGES3L, PTGES3L-AARSD1
    nsv5933022copy number variation1nstd209human GRCh38 chr17: 42,967,167-42,967,348 , GRCh37.p13 chr17: 41,119,184-41,119,365 PTGES3L-AARSD1, PTGES3L
    nsv5661849insertion1nstd207human GRCh38 chr17: 42,967,537-42,967,537 , GRCh37.p13 chr17: 41,119,554-41,119,554 PTGES3L, PTGES3L-AARSD1
    nsv5646965insertion2nstd207human GRCh38 chr17: 42,973,222-42,973,222 , GRCh37.p13 chr17: 41,125,239-41,125,239 PTGES3L-AARSD1, PTGES3L
    nsv5601219copy number variation1nstd207human GRCh38 chr17: 42,967,115-42,967,184 , GRCh37.p13 chr17: 41,119,132-41,119,201 PTGES3L-AARSD1, PTGES3L
    nsv5598914copy number variation1nstd207human GRCh38 chr17: 42,967,392-42,967,456 , GRCh37.p13 chr17: 41,119,409-41,119,473 PTGES3L-AARSD1, PTGES3L
    nsv5587099copy number variation1nstd207human GRCh38 chr17: 42,967,115-42,967,324 , GRCh37.p13 chr17: 41,119,132-41,119,341 PTGES3L, PTGES3L-AARSD1
    nsv5554090sequence alteration1nstd206human GRCh38 chr17: 32,109,732-67,925,723 , GRCh37.p13 chr17: 30,436,751-65,921,839 , APOH, 1099 more genes
    nsv5543402insertion1nstd206human GRCh38 chr17: 42,967,586-42,967,588 , GRCh37.p13 chr17: 41,119,603-41,119,605 PTGES3L, PTGES3L-AARSD1
    nsv5287669copy number variation1nstd204human GRCh38.p13 chr17: 42,963,201-43,231,700 , GRCh37.p13 chr17: 41,115,218-41,383,489 PTGES3L, CCDC200, 15 more genes
    nsv5159256mobile element insertion1nstd203human GRCh38 chr17: 42,978,077-42,978,097 , GRCh37.p13 chr17: 41,130,094-41,130,114 PTGES3L, PTGES3L-AARSD1
    nsv5156518mobile element insertion1nstd203human GRCh38 chr17: 42,966,244-42,966,261 , GRCh37.p13 chr17: 41,118,261-41,118,278 PTGES3L, PTGES3L-AARSD1
    nsv5154985mobile element insertion1nstd203human GRCh38 chr17: 42,969,009-42,969,017 , GRCh37.p13 chr17: 41,121,026-41,121,034 PTGES3L-AARSD1, PTGES3L
    nsv4766941insertion1nstd199human GRCh37 chr17: 41,125,196-41,125,196 , GRCh38.p12 chr17: 42,973,179-42,973,179 PTGES3L, PTGES3L-AARSD1
    nsv4737383copy number variation1nstd199human GRCh37 chr17: 41,119,154-41,119,225 , GRCh38.p12 chr17: 42,967,137-42,967,208 PTGES3L, PTGES3L-AARSD1
    nsv4510376mobile element insertion1nstd166human GRCh37.p13 chr17: 41,121,023-41,121,023 , GRCh38.p12 chr17: 42,969,006-42,969,006 PTGES3L-AARSD1, PTGES3L
    nsv4438445insertion1nstd175human GRCh37 chr17: 41,125,239-41,125,239 , GRCh38.p12 chr17: 42,973,222-42,973,222 PTGES3L, PTGES3L-AARSD1
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