ClinVar Miner

Submissions for variant GRCh37/hg19 16p13.11(chr16:16247252-16258276)x1

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Total submissions: 6
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
ARUP Laboratories, Cytogenetics and Genomic Microarray,ARUP Laboratories RCV000446824 SCV000501949 conflicting data from submitters See cases no assertion criteria provided clinical testing Uncertain significance(1), Likely benign (1)
Lineagen Inc. RCV000846137 SCV000988258 pathogenic not provided 2017-07-31 no assertion criteria provided clinical testing
Lineagen Inc. RCV000846961 SCV000989083 pathogenic not provided 2018-06-20 no assertion criteria provided clinical testing
Lineagen Inc. RCV000848030 SCV000990163 pathogenic not provided 2017-06-28 no assertion criteria provided clinical testing
Lineagen Inc. RCV000848588 SCV000990730 pathogenic not provided 2018-06-26 no assertion criteria provided clinical testing
Lineagen Inc. RCV000849321 SCV000991463 pathogenic not provided 2017-04-18 no assertion criteria provided clinical testing

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