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

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2685765	GRCh37/hg19 1q25.1(chr1:174507927-174675068)x1	RABGAP1L	Copy number loss	not provided	GUncertain significance
Select item 2685754	GRCh37/hg19 1q23.3-25.1(chr1:164571371-175708060)x1	ADCY10, ALDH9A1 +81 more	Copy number loss	not provided	GPathogenic
Select item 1341003	GRCh37/hg19 1q25.1(chr1:174330817-174607307)x1	GPR52, RABGAP1L	Copy number loss	not provided	GLikely benign
Select item 979311	GRCh37/hg19 1q25.1-25.3(chr1:173162501-182702252)x3	ABL2, ACBD6 +52 more	Copy number gain	not provided	GPathogenic
Select item 979310	GRCh37/hg19 1q25.1-25.2(chr1:174410914-178743636)x1	CACYBP, TEX35 +13 more	Copy number loss	not provided	GUncertain significance
Select item 814137	GRCh37/hg19 1q24.2-25.1(chr1:167430471-174635618)x1	METTL13, METTL18 +60 more	Copy number loss	not provided	GPathogenic
Select item 565198	GRCh37/hg19 1q25.1(chr1:174596959-174747357)x1	RABGAP1L	Copy number loss	not provided	GUncertain significance

ClinVar