ClinVar Miner

Submissions for variant GRCh37/hg19 Xp11.3(chrX:43396992-43626868)x2

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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 RCV000447431 SCV000502519 likely benign See cases no assertion criteria provided clinical testing
Quest Diagnostics Nichols Institute San Juan Capistrano RCV000684323 SCV000811832 uncertain significance not provided 2017-10-25 no assertion criteria provided clinical testing

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