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

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1808152	GRCh37/hg19 2q34(chr2:213290522-214539066)x3	ERBB4, IKZF2 +1 more	Copy number gain	not provided	GUncertain significance
Select item 980004	GRCh37/hg19 2q34-35(chr2:215122019-220397907)x1	AAMP, ABCA12 +66 more	Copy number loss	not provided	GLikely pathogenic
Select item 979402	GRCh37/hg19 2q34(chr2:214021457-214324932)x3	SPAG16	Copy number gain	not provided	GUncertain significance
Select item 979401	GRCh37/hg19 2q34(chr2:214763339-214900967)x1	SPAG16	Copy number loss	not provided	GUncertain significance
Select item 816572	GRCh37/hg19 2q34(chr2:214906879-215068829)x1	SPAG16	Copy number loss	not provided	GLikely benign
Select item 814364	GRCh37/hg19 2q34(chr2:214769083-215110737)x3	SPAG16	Copy number gain	not provided	GLikely benign
Select item 562677	GRCh37/hg19 2q33.3-35(chr2:205169148-219149293)x3	AAMP, ABCA12 +60 more	Copy number gain	not provided	GPathogenic
Select item 562620	GRCh37/hg19 2q34(chr2:213969855-214925262)x3	SPAG16, IKZF2	Copy number gain	not provided	GLikely benign
Select item 562558	GRCh37/hg19 2q34(chr2:214766288-215035184)x4	SPAG16	Copy number gain	not provided	GLikely benign

ClinVar