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

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1809379	GRCh37/hg19 7p15.2-14.3(chr7:27133786-34466477)x1	ADCYAP1R1, AQP1 +50 more	Copy number loss	not provided	GPathogenic
Select item 1808748	GRCh37/hg19 7p15.2-15.1(chr7:26418391-28323299)x3	EVX1, HIBADH +19 more	Copy number gain	not provided	GUncertain significance
Select item 1808022	GRCh37/hg19 7p15.2-15.1(chr7:27591948-28096955)x1	HIBADH, JAZF1 +1 more	Copy number loss	not provided	GUncertain significance
Select item 1340835	GRCh37/hg19 7p15.2-15.1(chr7:27902401-28202571)x3	JAZF1	Copy number gain	not provided	GUncertain significance
Select item 814947	GRCh37/hg19 7p15.3-14.3(chr7:23877135-33139446)x1	FKBP14, HNRNPA2B1 +61 more	Copy number loss	not provided	GPathogenic
Select item 563311	GRCh37/hg19 7p15.2-15.1(chr7:27924232-28080968)x1	JAZF1	Copy number loss	not provided	GUncertain significance

ClinVar