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

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
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 1808267	GRCh37/hg19 1q24.2(chr1:168675820-169363333)x1	ATP1B1, BLZF1 +2 more	Copy number loss	not provided	GUncertain significance
Select item 979304	GRCh37/hg19 1q24.2(chr1:169205727-169383182)x1	BLZF1, NME7 +1 more	Copy number loss	not provided	GUncertain significance
Select item 979302	GRCh37/hg19 1q23.3-24.2(chr1:164608682-169216098)x1	STYXL2, GPR161 +30 more	Copy number loss	not provided	GLikely pathogenic
Select item 814139	GRCh37/hg19 1q24.2(chr1:169148346-169806006)x1	C1orf112, NME7 +8 more	Copy number loss	not provided	GUncertain significance
Select item 814138	GRCh37/hg19 1q24.2(chr1:169126894-169278743)x1	NME7	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

ClinVar