"Bionano Laboratories"[submitter] AND "COMT"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 689137	GRCh37/hg19 22q11.21(chr22:19932833-19945742)x1	COMT	Copy number loss	not provided	GUncertain significance
Select item 688754	GRCh37/hg19 22q11.21(chr22:18916827-20311858)x1	ARVCF, C22orf39 +26 more	Copy number loss	not provided	GPathogenic
Select item 688248	GRCh37/hg19 22q11.21(chr22:19905801-19938011)x3	COMT, TXNRD2	Copy number gain	not provided	GUncertain significance
Select item 686107	GRCh37/hg19 22q11.1-11.21(chr22:16888899-20312661)x3	ADA2, ARVCF +44 more	Copy number gain	not provided	GPathogenic
Select item 685644	GRCh37/hg19 22q11.21(chr22:18916842-20311858)x1	ARVCF, C22orf39 +26 more	Copy number loss	not provided	GPathogenic
Select item 685636	GRCh37/hg19 22q11.1-13.33(chr22:16888899-51197838)x3	TUBA8, TUBGCP6 +435 more	Copy number gain	not provided	GPathogenic
Select item 684996	GRCh37/hg19 22q11.1-11.21(chr22:17055733-20312661)x3	ADA2, ARVCF +44 more	Copy number gain	not provided	GPathogenic

ClinVar