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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7139033copy number variation1nstd232human GRCh37.p13 chr17: 39,967,285-39,967,381 , GRCh38.p12 chr17: 41,811,033-41,811,129 P3H4, FKBP10
    nsv7094885copy number variation1nstd102humanPathogenic GRCh37 chr17: 39,969,287-39,969,551 , GRCh38.p12 chr17: 41,813,035-41,813,299 P3H4, FKBP10
    nsv6984984copy number variation1nstd229human GRCh38 chr17: 38,377,708-42,855,253 , GRCh37.p13 chr17: 36,701,616-41,007,270 ZNF385C, AOC2, 248 more genes
    nsv6982861copy number variation1nstd229human GRCh38 chr17: 38,291,672-47,498,259 , GRCh37.p13 chr17: 36,510,266-45,575,625 KRT20, PLEKHH3, 442 more genes
    nsv6980021copy number variation1nstd229human GRCh38 chr17: 41,798,112-41,802,403 , GRCh37.p13 chr17: 39,954,364-39,958,655 , GRCh37.p13 chr17|NW_003571052.1: 84,754-89,045 P3H4
    nsv6507232copy number variation1nstd223human GRCh38 chr17: 41,798,044-41,802,399 , GRCh37.p13 chr17|NW_003571052.1: 84,686-89,041 , GRCh37.p13 chr17: 39,954,296-39,958,651 P3H4
    nsv6503270copy number variation1nstd223human GRCh38 chr17: 41,802,835-41,804,186 , GRCh37.p13 chr17: 39,959,087-39,960,438 , GRCh37.p13 chr17|NW_003571052.1: 89,477-90,828 P3H4
    nsv6498736copy number variation1nstd223human GRCh38 chr17: 41,808,695-41,809,550 , GRCh37.p13 chr17|NW_003571052.1: 95,337-96,192 , GRCh37.p13 chr17: 39,964,947-39,965,802 P3H4
    nsv6310304copy number variation1nstd102humanUncertain significance GRCh37 chr17: 39,923,611-39,978,660 , GRCh38.p12 chr17: 41,767,359-41,822,408 P3H4, JUP, 1 more genes
    nsv6133357copy number variation1nstd213human GRCh37 chr17: 39,920,000-40,260,001 , GRCh38.p12 chr17: 41,763,748-42,107,983 ACLY, CNP, 12 more genes
    nsv6133061copy number variation1nstd213human GRCh37 chr17: 39,870,000-40,890,001 , GRCh38.p12 chr17: 41,713,748-42,737,983 ACLY, ATP6V0A1, 51 more genes
    nsv6133060copy number variation1nstd213human GRCh37 chr17: 39,870,000-40,880,001 , GRCh38.p12 chr17: 41,713,748-42,727,983 ACLY, ATP6V0A1, 51 more genes
    nsv5937330copy number variation1nstd209human GRCh38 chr17: 41,798,055-41,802,453 , GRCh37.p13 chr17|NW_003571052.1: 84,697-89,095 , GRCh37.p13 chr17: 39,954,307-39,958,705 P3H4
    nsv5927785copy number variation1nstd209human GRCh38 chr17: 41,808,695-41,809,549 , GRCh37.p13 chr17|NW_003571052.1: 95,337-96,191 , GRCh37.p13 chr17: 39,964,947-39,965,801 P3H4
    nsv5885743copy number variation1nstd209human GRCh38 chr17: 41,798,091-41,802,424 , GRCh37.p13 chr17|NW_003571052.1: 84,733-89,066 , GRCh37.p13 chr17: 39,954,343-39,958,676 P3H4
    nsv5554090sequence alteration1nstd206human GRCh38 chr17: 32,109,732-67,925,723 , GRCh37.p13 chr17: 30,436,751-65,921,839 , APOH, 1099 more genes
    nsv5531977copy number variation1nstd206human GRCh38 chr17: 41,808,698-41,809,550 , GRCh37.p13 chr17|NW_003571052.1: 95,340-96,192 , GRCh37.p13 chr17: 39,964,950-39,965,802 P3H4
    nsv5527321copy number variation1nstd206human GRCh38 chr17: 41,798,094-41,802,440 , GRCh37.p13 chr17|NW_003571052.1: 84,736-89,082 , GRCh37.p13 chr17: 39,954,346-39,958,692 P3H4
    nsv5016398copy number variation1nstd200human GRCh38 chr17: 41,802,833-41,804,187 , GRCh37.p13 chr17|NW_003571052.1: 89,475-90,829 , GRCh37.p13 chr17: 39,959,085-39,960,439 P3H4
    nsv5016397copy number variation1nstd200human GRCh38 chr17: 41,798,085-41,802,409 , GRCh37.p13 chr17|NW_003571052.1: 84,727-89,051 , GRCh37.p13 chr17: 39,954,337-39,958,661 P3H4
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