ClinVar Miner

Submissions for variant GRCh37/hg19 9p23-22.2(chr9:13638428-17121764)x1

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Department of Medical Genetics, Oslo University Hospital RCV001263226 SCV001437591 pathogenic Chromosome 9p deletion syndrome no assertion criteria provided clinical testing

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