ClinVar Miner

Submissions for variant GRCh37/hg19 1q21.1-21.2(chr1:146521698-147721869)x1

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Centro Nacional de Genética Medica "Dr. Eduardo E. Castilla", Administración Nacional de Laboratorios e Institutos de Salud RCV000856631 SCV000966002 pathogenic Chromosome 1q21.1 deletion syndrome 2019-01-01 criteria provided, single submitter clinical testing

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