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

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1808382	GRCh37/hg19 3p21.1-14.3(chr3:54380659-54436878)x1	CACNA2D3	Copy number loss	not provided	GUncertain significance
Select item 1340126	GRCh37/hg19 3p21.1-14.3(chr3:54370192-54625132)x1	CACNA2D3	Copy number loss	not provided	GUncertain significance
Select item 980507	GRCh37/hg19 3p14.3(chr3:54975766-55100284)x1	CACNA2D3	Copy number loss	not provided	GUncertain significance
Select item 814446	GRCh37/hg19 3p14.3(chr3:54707598-54828067)x1	CACNA2D3	Copy number loss	not provided	GUncertain significance
Select item 814445	GRCh37/hg19 3p21.1-14.3(chr3:54364992-55064740)x1	CACNA2D3, ESRG +1 more	Copy number loss	not provided	GUncertain significance
Select item 562770	GRCh37/hg19 3p14.3(chr3:54793252-54931307)x1	CACNA2D3	Copy number loss	not provided	GUncertain significance
Select item 562769	GRCh37/hg19 3p21.1(chr3:53892719-54182466)x3	SELENOK, IL17RB +2 more	Copy number gain	not provided	GLikely benign

ClinVar