ClinVar Miner

Submissions for variant GRCh37/hg19 18q22.1-23(chr18:66459747-78012829)x1

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Medicover Genetics GmbH, Medicover Humangenetik Berlin-Lichtenberg MVZ RCV003225711 SCV003915778 pathogenic Deletion of long arm of chromosome 18 2023-01-31 no assertion criteria provided clinical testing

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