Related gene-specific medical variations for Gene (Select 131368) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1527034	GRCh37/hg19 3q12.3-13.11(chr3:102025967-103468070)	ZPLD1	Copy number gain	not specified	GUncertain significance
Select item 1340214	GRCh37/hg19 3q12.3(chr3:101892890-102296491)x1	ZPLD1	Copy number loss	not provided	GUncertain significance
Select item 686856	GRCh37/hg19 3q12.3(chr3:102129345-102201538)x1	ZPLD1	Copy number loss	not provided	GUncertain significance
Select item 562797	GRCh37/hg19 3q12.3(chr3:102078343-102293262)x1	ZPLD1	Copy number loss	not provided	GLikely benign

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