ClinVar Miner

Variants studied for global developmental delay with speech and behavioral abnormalities

Included ClinVar conditions (2):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:

If a variant has more than one submission, it may be counted in more than one significance column. If this is the case, the total number of variants will be less than the sum of the other cells.

pathogenic likely pathogenic uncertain significance likely benign benign total
14 12 37 1 0 64

Gene and significance breakdown #

Total genes and gene combinations: 1
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Gene or gene combination pathogenic likely pathogenic uncertain significance likely benign total
TNRC6B 14 12 37 1 64

Submitter and significance breakdown #

Total submitters: 28
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Submitter pathogenic likely pathogenic uncertain significance likely benign total
Revvity Omics, Revvity 0 0 7 0 7
OMIM 6 0 0 0 6
Neuberg Centre For Genomic Medicine, NCGM 0 1 5 0 6
Center for Genomic Medicine, King Faisal Specialist Hospital and Research Center 0 0 5 0 5
Victorian Clinical Genetics Services, Murdoch Childrens Research Institute 1 0 3 0 4
New York Genome Center 0 0 4 0 4
Baylor Genetics 0 1 2 0 3
Foundation for Research in Genetics and Endocrinology, FRIGE's Institute of Human Genetics 0 0 3 0 3
Juno Genomics, Hangzhou Juno Genomics, Inc 1 0 2 0 3
Institute of Medical Genetics and Applied Genomics, University Hospital Tübingen 2 1 0 0 3
Institute of Human Genetics, University of Goettingen 0 1 1 0 2
Clinical Genomics Laboratory, Washington University in St. Louis 0 1 1 0 2
Equipe Genetique des Anomalies du Developpement, Université de Bourgogne 0 1 1 0 2
3billion 1 0 0 1 2
Greenwood Genetic Center Diagnostic Laboratories, Greenwood Genetic Center 0 1 0 0 1
MGZ Medical Genetics Center 0 0 1 0 1
Women's Health and Genetics/Laboratory Corporation of America, LabCorp 1 0 0 0 1
Institute for Human Genetics and Genomic Medicine, Uniklinik RWTH Aachen 0 1 0 0 1
Institute of Human Genetics, University Hospital of Duesseldorf 0 0 1 0 1
Institute of Human Genetics, University of Leipzig Medical Center 1 0 0 0 1
Laboratoire de Génétique Moléculaire, CHU Bordeaux 0 1 0 0 1
Pittsburgh Clinical Genomics Laboratory, University of Pittsburgh Medical Center 0 1 0 0 1
Institute of Human Genetics, Clinical Exome/Genome Diagnostics Group, University Hospital Bonn 0 0 1 0 1
Clinical Genetics Laboratory, University Hospital Schleswig-Holstein 1 0 0 0 1
Department of Human Genetics, Hannover Medical School 0 1 0 0 1
Laboratorio de Genetica e Diagnostico Molecular, Hospital Israelita Albert Einstein 0 0 1 0 1
Breakthrough Genomics, Breakthrough Genomics 0 1 0 0 1
Tammimies Lab, Karolinska Institutet 1 0 0 0 1

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