ClinVar Miner

Submissions for variant GRCh37/hg19 2q34(chr2:213969855-214925262)x3

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
ARUP Laboratories, Cytogenetics and Genomic Microarray,ARUP Laboratories RCV000448179 SCV000502013 uncertain significance See cases no assertion criteria provided clinical testing
Quest Diagnostics Nichols Institute San Juan Capistrano RCV000682109 SCV000809616 likely benign not provided 2017-10-05 no assertion criteria provided clinical testing

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