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

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2684871	GRCh37/hg19 18q11.2(chr18:20920907-21418343)x3	ANKRD29, LAMA3 +4 more	Copy number gain	not provided	GUncertain significance
Select item 2684870	GRCh37/hg19 18q11.2(chr18:20727902-21021472)x3	CABLES1, TMEM241	Copy number gain	not provided	GUncertain significance
Select item 2684869	GRCh37/hg19 18q11.2(chr18:20727641-21033786)x3	CABLES1, RIOK3 +1 more	Copy number gain	not provided	GUncertain significance
Select item 1340068	GRCh37/hg19 18q11.1-12.1(chr18:18611942-26843691)x3	ABHD3, ANKRD29 +29 more	Copy number gain	not provided	GUncertain significance
Select item 1340066	GRCh37/hg19 18p11.32-q12.1(chr18:136226-25252276)x3	ABHD3, ADCYAP1 +95 more	Copy number gain	not provided	GPathogenic
Select item 979687	GRCh37/hg19 18q11.2(chr18:20904405-20971321)x1	TMEM241	Copy number loss	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 815991	GRCh37/hg19 18q11.2(chr18:20958811-21082161)x1	TMEM241, RIOK3	Copy number loss	not provided	GLikely benign
Select item 564547	GRCh37/hg19 18q11.2(chr18:20803607-24109364)x1	HRH4, ZNF521 +15 more	Copy number loss	not provided	GUncertain significance

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