ClinVar Miner

Submissions for variant GRCh37/hg19 18q11.2(chr18:21116657-21146846)x3

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Total submissions: 1

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Submitter	RCV	SCV	Clinical significance	Condition	Last evaluated	Review status	Method	Comment
ARUP Laboratories, Cytogenetics and Genomic Microarray,ARUP Laboratories	RCV000446304	SCV000501462	uncertain significance	See cases		no assertion criteria provided	clinical testing

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