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

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1808967	GRCh37/hg19 2p22.1(chr2:39266694-39622510)x1	CDKL4, MAP4K3 +1 more	Copy number loss	not provided	GUncertain significance
Select item 979968	GRCh37/hg19 2p22.2-22.1(chr2:38012532-39548268)x3	GALM, SRSF7 +12 more	Copy number gain	not provided	GUncertain significance
Select item 814239	GRCh37/hg19 2p22.1(chr2:39578669-40167082)x3	THUMPD2, MAP4K3 +1 more	Copy number gain	not provided	GUncertain significance
Select item 814238	GRCh37/hg19 2p22.1(chr2:39264474-39626960)x3	SOS1, CDKL4 +1 more	Copy number gain	not provided	GLikely benign
Select item 814237	GRCh37/hg19 2p22.1(chr2:39261250-39626960)x3	SOS1, CDKL4 +1 more	Copy number gain	not provided	GLikely benign
Select item 814236	GRCh37/hg19 2p22.1(chr2:39261250-39631150)x3	CDKL4, SOS1 +1 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 562491	GRCh37/hg19 2p22.1(chr2:39496232-39558820)x1	MAP4K3	Copy number loss	not provided	GUncertain significance

ClinVar