Related gene-specific medical variations for Gene (Select 84083) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 980589	GRCh37/hg19 2q21.3(chr2:136037258-136225722)x1	ZRANB3	Copy number loss	not provided	GUncertain significance
Select item 980588	GRCh37/hg19 2q21.3(chr2:136091663-136155577)x1	ZRANB3	Copy number loss	not provided	GUncertain significance
Select item 814308	GRCh37/hg19 2q21.3(chr2:136071023-136243048)x1	ZRANB3	Copy number loss	not provided	GUncertain significance
Select item 152544	GRCh38/hg38 2q21.3(chr2:135479205-135518855)x1	ZRANB3	Copy number loss	See cases	GLikely benign

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