Variants studied for Microcephaly 7, primary, autosomal recessive

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		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	not provided	total
5	7	92	7	10	10	123

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	benign	not provided	total
STIL	5	7	92	7	10	10	123

Submitter and significance breakdown #

Total submitters: 20

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Submitter	pathogenic	likely pathogenic	uncertain significance	likely benign	benign	not provided	total
Illumina Laboratory Services, Illumina	0	0	64	4	10	0	78
Genetic Services Laboratory, University of Chicago	0	1	13	0	0	0	14
Fulgent Genetics, Fulgent Genetics	0	0	9	1	0	0	10
GeneReviews	0	0	0	0	0	9	9
OMIM	5	0	0	0	0	0	5
Baylor Genetics	0	0	5	0	0	0	5
Revvity Omics, Revvity	0	1	4	0	0	0	5
Mendelics	0	0	0	2	1	0	3
Diagnostic Laboratory, Department of Genetics, University Medical Center Groningen	0	0	0	0	3	0	3
Genome-Nilou Lab	0	0	0	0	3	0	3
Department of Clinical Genetics, Copenhagen University Hospital, Rigshospitalet	0	1	1	0	0	0	2
Precision Medical Center, Maternal and Child Health Hospital of Hubei Province	0	2	0	0	0	0	2
3billion	0	1	1	0	0	0	2
Neuberg Centre For Genomic Medicine, NCGM	0	0	2	0	0	0	2
Women's Health and Genetics/Laboratory Corporation of America, LabCorp	0	1	0	0	0	0	1
Knight Diagnostic Laboratories, Oregon Health and Sciences University	0	0	1	0	0	0	1
Daryl Scott Lab, Baylor College of Medicine	0	0	1	0	0	0	1
Institute of Human Genetics, University of Leipzig Medical Center	0	0	1	0	0	0	1
Broad Center for Mendelian Genomics, Broad Institute of MIT and Harvard	0	0	1	0	0	0	1
GenomeConnect - Brain Gene Registry	0	0	0	0	0	1	1

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