ClinVar Miner

Submissions for variant GRCh37/hg19 14q31.3(chr14:88400251-88422569)x1

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
ARUP Laboratories, Cytogenetics and Genomic Microarray,ARUP Laboratories RCV000446983 SCV000501468 conflicting data from submitters See cases no assertion criteria provided clinical testing Uncertain significance(2), Likely benign (1)
Lineagen, Inc RCV000845846 SCV000987967 pathogenic not provided 2017-09-26 no assertion criteria provided clinical testing
Lineagen, Inc RCV000846474 SCV000988596 pathogenic not provided 2018-04-25 no assertion criteria provided clinical testing

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