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

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1341024	GRCh37/hg19 7q21.11(chr7:82958543-84062357)x3	SEMA3A, SEMA3E	Copy number gain	not provided	GUncertain significance
Select item 1340282	GRCh37/hg19 7q21.11(chr7:82757837-83073851)x3	PCLO, SEMA3E	Copy number gain	not provided	GUncertain significance
Select item 815006	GRCh37/hg19 7q21.11(chr7:83118607-83183333)x1	SEMA3E	Copy number loss	not provided	GUncertain significance
Select item 815005	GRCh37/hg19 7q21.11(chr7:82653019-83691163)x3	SEMA3A, SEMA3E +1 more	Copy number gain	not provided	GUncertain significance
Select item 815003	GRCh37/hg19 7q21.11(chr7:82243367-83600926)x1	SEMA3A, SEMA3E +1 more	Copy number loss	not provided	GUncertain significance
Select item 563384	GRCh37/hg19 7q21.11(chr7:82922936-83829252)x3	SEMA3E, SEMA3A	Copy number gain	not provided	GUncertain significance
Select item 563294	GRCh37/hg19 7q21.11(chr7:82969760-83073851)x1	SEMA3E	Copy number loss	not provided	GUncertain significance

ClinVar