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

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1808221	GRCh37/hg19 18q21.1(chr18:46379233-46777416)x3	CTIF, DYM +1 more	Copy number gain	not provided	GUncertain significance
Select item 1340243	GRCh37/hg19 18q21.1(chr18:46379233-46642420)x3	CTIF, DYM +1 more	Copy number gain	not provided	GUncertain significance
Select item 816014	GRCh37/hg19 18q11.2-21.2(chr18:20689919-49455212)x3	ACAA2, ANKRD29 +97 more	Copy number gain	not provided	GPathogenic
Select item 564571	GRCh37/hg19 18q21.1-23(chr18:46942427-78014123)x1	ACAA2, ADNP2 +107 more	Copy number loss	not provided	GPathogenic
Select item 564568	GRCh37/hg19 18q12.2-21.31(chr18:35866313-55082983)x3	ACAA2, ATP5F1A +55 more	Copy number gain	not provided	GPathogenic
Select item 564506	GRCh37/hg19 18q21.1(chr18:46379232-46778031)x3	DYM, CTIF +1 more	Copy number gain	not provided	GUncertain significance
Select item 564492	GRCh37/hg19 18q21.1(chr18:46583722-46803612)x1	DYM	Copy number loss	not provided	GUncertain significance
Select item 564485	GRCh37/hg19 18q21.1(chr18:46674881-46750191)x1	DYM	Copy number loss	not provided	GUncertain significance

ClinVar