ClinVar Miner

Submissions for variant GRCh37/hg19 5p15.1(chr5:15086014-15868591)x3

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Cytogenetics, Genetics Associates, Inc. RCV002287836 SCV002577656 uncertain significance DiGeorge syndrome no assertion criteria provided clinical testing

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