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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