"Illumina Laboratory Services, Illumina"[submitter] AND "ARMCX5-GPRASP - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1299435	NM_001184727.2(GPRASP1):c.197T>A (p.Val66Asp)	GPRASP1, ARMCX5-GPRASP2 (V66D)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 1710513	GRCh37/hg19 Xq21.1-24(chrX:76794355-119282836)x3	CAPN6, CENPI +176 more	Copy number gain	not provided	GPathogenic
Select item 1180551	GRCh37/hg19 Xp22.33-q28(chrX:60000-155234966)x1	CXorf49B, CXorf51A +821 more	Copy number loss	not provided	GPathogenic

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