"Quest Diagnostics Nichols Institute San Juan Capistrano"[submitter] A - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 89155	NM_000179.3(MSH6):c.*85T>A	FBXO11, MSH6	Single nucleotide variant (3 prime UTR variant +2 more)	Hereditary cancer-predisposing syndrome +5 more	GConflicting classifications of pathogenicity
Select item 1341006	GRCh37/hg19 2p21-16.3(chr2:47550425-48041798)x3	BCYRN1, EPCAM +5 more	Copy number gain	not provided	GUncertain significance
Select item 979359	GRCh37/hg19 2p21-16.3(chr2:47469710-48143700)x3	KCNK12, BCYRN1 +5 more	Copy number gain	not provided	GUncertain significance
Select item 562680	GRCh37/hg19 2p22.3-16.1(chr2:34792916-56676541)x3	ABCG5, ABCG8 +100 more	Copy number gain	not provided	GPathogenic
Select item 562629	GRCh37/hg19 2p21-16.3(chr2:46978055-48131152)x3	EPCAM, FBXO11 +10 more	Copy number gain	not provided	GUncertain significance
Select item 562548	GRCh37/hg19 2p16.3(chr2:47868692-48091913)x3	FBXO11, MSH6	Copy number gain	not provided	GUncertain significance

ClinVar