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

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Items: 5

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2684602	GRCh37/hg19 10q11.21-24.2(chr10:42709645-100834951)x3	RRP12, RTKN2 +332 more	Copy number gain	not provided	GPathogenic
Select item 979284	GRCh37/hg19 10q24.1(chr10:97452629-97616981)x1	TCTN3, ENTPD1	Copy number loss	not provided	GUncertain significance
Select item 563802	GRCh37/hg19 10q23.33-26.3(chr10:94346520-135427143)x3	ABCC2, ABLIM1 +298 more	Copy number gain	not provided	GPathogenic
Select item 563744	GRCh37/hg19 10q24.1(chr10:97333368-97737323)x1	ALDH18A1, C10orf131 +2 more	Copy number loss	not provided	GUncertain significance
Select item 563693	GRCh37/hg19 10q24.1(chr10:97514458-97576041)x1	ENTPD1	Copy number loss	not provided	GLikely benign

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