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

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 980173	GRCh37/hg19 5q21.3(chr5:107306322-107623501)x1	FBXL17	Copy number loss	not provided	GUncertain significance
Select item 814720	GRCh37/hg19 5q21.3(chr5:107168048-107526811)x3	FBXL17	Copy number gain	not provided	GLikely benign
Select item 563099	GRCh37/hg19 5q21.3(chr5:106265124-107656892)x1	FBXL17, EFNA5	Copy number loss	not provided	GLikely benign

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