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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7077064inversion1nstd229human GRCh38 chr19: 32,615,349-32,618,046 , GRCh37.p13 chr19: 33,106,255-33,108,952 ANKRD27
    nsv7076013inversion1nstd229human GRCh38 chr19: 32,611,147-32,623,012 , GRCh37.p13 chr19: 33,102,053-33,113,918 ANKRD27
    nsv7064982inversion1nstd229human GRCh38 chr19: 32,032,146-33,117,941 , GRCh37.p13 chr19: 32,523,052-33,608,847 LINC01782, NUDT19, 22 more genes
    nsv7017233copy number variation1nstd229human GRCh38 chr19: 32,635,562-32,651,628 , GRCh37.p13 chr19: 33,126,468-33,142,534 ANKRD27, RPS12P31
    nsv7015578copy number variation1nstd229human GRCh38 chr19: 32,625,570-32,627,539 , GRCh37.p13 chr19: 33,116,476-33,118,445 ANKRD27
    nsv7014908copy number variation1nstd229human GRCh38 chr19: 32,487,678-32,863,605 , GRCh37.p13 chr19: 32,978,584-33,354,511 RN7SKP22, SNORA68B, 9 more genes
    nsv7014218copy number variation1nstd229human GRCh38 chr19: 32,650,153-32,667,375 , GRCh37.p13 chr19: 33,141,059-33,158,281 RN7SL789P, ANKRD27
    nsv7013822copy number variation1nstd229human GRCh38 chr19: 32,624,757-32,625,924 , GRCh37.p13 chr19: 33,115,663-33,116,830 ANKRD27
    nsv7013549copy number variation1nstd229human GRCh38 chr19: 32,611,483-32,663,805 , GRCh37.p13 chr19: 33,102,389-33,154,711 RN7SL789P, ANKRD27, 1 more genes
    nsv7013346copy number variation1nstd229human GRCh38 chr19: 32,608,738-32,615,666 , GRCh37.p13 chr19: 33,099,644-33,106,572 ANKRD27, SNORA68B
    nsv7012940copy number variation1nstd229human GRCh38 chr19: 32,627,693-32,630,882 , GRCh37.p13 chr19: 33,118,599-33,121,788 ANKRD27
    nsv7011886copy number variation1nstd229human GRCh38 chr19: 32,626,502-32,626,538 , GRCh37.p13 chr19: 33,117,408-33,117,444 ANKRD27
    nsv7007180copy number variation1nstd229human GRCh38 chr19: 32,607,834-32,615,657 , GRCh37.p13 chr19: 33,098,740-33,106,563 SNORA68B, ANKRD27
    nsv7006333copy number variation1nstd229human GRCh38 chr19: 32,596,090-32,596,576 , GRCh37.p13 chr19: 33,086,996-33,087,482 ANKRD27
    nsv7005570copy number variation1nstd229human GRCh38 chr19: 32,618,147-32,618,318 , GRCh37.p13 chr19: 33,109,053-33,109,224 ANKRD27
    nsv7004394copy number variation1nstd229human GRCh38 chr19: 32,605,449-32,616,776 , GRCh37.p13 chr19: 33,096,355-33,107,682 SNORA68B, ANKRD27
    nsv7004060copy number variation1nstd229human GRCh38 chr19: 32,675,101-32,677,500 , GRCh37.p13 chr19: 33,166,007-33,168,406 ANKRD27, RGS9BP
    nsv7003951copy number variation1nstd229human GRCh38 chr19: 32,620,841-32,650,597 , GRCh37.p13 chr19: 33,111,747-33,141,503 RPS12P31, ANKRD27
    nsv7003189copy number variation1nstd229human GRCh38 chr19: 32,661,101-32,669,800 , GRCh37.p13 chr19: 33,152,007-33,160,706 ANKRD27
    nsv7000909copy number variation1nstd229human GRCh38 chr19: 32,668,301-32,681,700 , GRCh37.p13 chr19: 33,159,207-33,172,606 RGS9BP, ANKRD27
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