ClinVar Miner

Submissions for variant GRCh37/hg19 8q21.11-21.3(chr8:75904944-87097083)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 RCV002279750 SCV002098079 pathogenic Chromosome 8q21.11 deletion syndrome 2022-02-02 criteria provided, single submitter clinical testing

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