ClinVar Miner

Submissions for variant GRCh37/hg19 4p16.3-16.1(chr4:68345-8731855)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 RCV000447633 SCV000502940 pathogenic See cases no assertion criteria provided clinical testing
ISCA site 1 RCV000510565 SCV000586666 likely pathogenic See cases 2014-05-05 no assertion criteria provided clinical testing

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