"GeneDx"[submitter] AND "PNLIP"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 432668	NM_000936.4(PNLIP):c.526G>A (p.Gly176Arg)	PNLIP (G176R)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 253831	GRCh37/hg19 10q25.3(chr10:118327326-118486839)x1	HSPA12A, C10orf82 +3 more	Copy number loss	See cases	GUncertain significance
Select item 253479	GRCh37/hg19 10q24.32-26.3(chr10:103288313-135512075)x3	ABLIM1, ABRAXAS2 +201 more	Copy number gain	See cases	GPathogenic

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