ClinVar Miner

Submissions for variant NC_000022.10:g.(21822774_21914652)_(22922798_23025613)del

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Centre of Medical Genetics, University of Antwerp RCV001199824 SCV001190346 pathogenic Chromosome 22q11.2 deletion syndrome, distal 2019-12-16 criteria provided, single submitter research

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