ClinVar Miner

Submissions for variant GRCh38/hg38 19p13.12-13.11(chr19:15014099-16261691)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Daryl Scott Lab, Baylor College of Medicine RCV003223562 SCV003919110 pathogenic Chromosome 19p13.13 deletion syndrome 2023-08-14 criteria provided, single submitter curation 1A, 2A, 3B (1.45)

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