ClinVar Miner

Submissions for variant GRCh37/hg19 1q43(chr1:240407420-240835685)x3

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
ARUP Laboratories, Cytogenetics and Genomic Microarray, ARUP Laboratories RCV003987050 SCV004801982 uncertain significance not specified criteria provided, single submitter clinical testing

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