"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 2685608	GRCh37/hg19 17q25.1(chr17:71337404-71416350)x1	SDK2	Copy number loss	not provided	GUncertain significance
Select item 2685607	GRCh37/hg19 17q24.3-25.1(chr17:69501527-71380722)x1	CDC42EP4, COG1 +7 more	Copy number loss	not provided	GPathogenic
Select item 564469	GRCh37/hg19 17q25.1(chr17:71298656-71527253)x3	SDK2, CDC42EP4	Copy number gain	not provided	GLikely benign
Select item 564463	GRCh37/hg19 17q24.1-25.3(chr17:63689671-81041938)x3	AANAT, AATK +222 more	Copy number gain	not provided	GPathogenic

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ClinVar