Variants in gene NCOR1 - ClinVar Miner

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
0	1	160	24	23	1	206

Condition and significance breakdown #

Total conditions: 10

Download table as spreadsheet

Condition	likely pathogenic	uncertain significance	likely benign	benign	not provided	total
not specified	0	146	2	0	0	148
NCOR1-related disorder	0	5	16	21	0	42
not provided	0	4	7	14	1	26
Autism spectrum disorder	0	1	0	0	0	1
Breast ductal adenocarcinoma	0	1	0	0	0	1
Familial cancer of breast	0	1	0	0	0	1
NCOR1-related Neurodevelopmental disorder	0	1	0	0	0	1
NCOR1-related autism spectrum disorder	0	1	0	0	0	1
See cases	0	1	0	0	0	1
Thin skin; Developmental delay; Hyperlaxity	1	0	0	0	0	1

Submitter and significance breakdown #

Total submitters: 14

Download table as spreadsheet

Submitter	likely pathogenic	uncertain significance	likely benign	benign	not provided	total
Ambry Genetics	0	145	2	0	0	147
PreventionGenetics, part of Exact Sciences	0	5	16	21	0	42
Labcorp Genetics (formerly Invitae), Labcorp	0	0	4	14	0	18
Breakthrough Genomics, Breakthrough Genomics	0	0	0	7	0	7
CeGaT Center for Human Genetics Tuebingen	0	2	3	1	0	6
New York Genome Center	0	3	0	0	0	3
GeneDx	0	1	0	0	0	1
Clinical Genomics Laboratory, Washington University in St. Louis	0	1	0	0	0	1
Next Generation Diagnostics, Novartis Institutes for BioMedical Research, Inc.	0	1	0	0	0	1
Faculty of Pharmacy, Medical University of Gdansk	0	1	0	0	0	1
Caryl and Israel Englander Institute for Precision Medicine, Weill Cornell Medicine	0	1	0	0	0	1
Laboratoire de cytogenetique, Hopital Necker-Enfants Malades	1	0	0	0	0	1
MutSpliceDB: a database of splice sites variants effects on splicing, NIH	0	0	0	0	1	1
Oasi Research Institute-IRCCS	0	1	0	0	0	1

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.