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

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2684481	GRCh37/hg19 7p21.3(chr7:11017837-11580072)x3	PHF14, THSD7A	Copy number gain	not provided	GUncertain significance
Select item 1341133	GRCh37/hg19 7p21.3-21.1(chr7:7909867-17213072)x1	AGMO, AGR2 +20 more	Copy number loss	not provided	GUncertain significance
Select item 980254	GRCh37/hg19 7p21.3(chr7:10712710-11500366)x3	THSD7A, PHF14 +1 more	Copy number gain	not provided	GUncertain significance
Select item 980251	GRCh37/hg19 7p21.3(chr7:11405926-11636997)x3	THSD7A	Copy number gain	not provided	GLikely benign
Select item 980250	GRCh37/hg19 7p21.3(chr7:10528678-11457492)x3	THSD7A, PHF14 +1 more	Copy number gain	not provided	GLikely benign
Select item 814933	GRCh37/hg19 7p21.3(chr7:11514979-11580072)x1	THSD7A	Copy number loss	not provided	GLikely benign
Select item 814932	GRCh37/hg19 7p21.3(chr7:10116563-11737690)x3	THSD7A, NDUFA4 +1 more	Copy number gain	not provided	GUncertain significance
Select item 563374	GRCh37/hg19 7p21.3(chr7:10866366-11568530)x3	PHF14, THSD7A +1 more	Copy number gain	not provided	GLikely benign

ClinVar