Related gene-specific medical variations for Gene (Select 153020) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1808766	GRCh37/hg19 4q21.21-21.22(chr4:82377883-82417592)x1	RASGEF1B	Copy number loss	not provided	GUncertain significance
Select item 980100	GRCh37/hg19 4q21.21-21.22(chr4:82377883-82602075)x3	RASGEF1B	Copy number gain	not provided	GUncertain significance
Select item 443689	GRCh37/hg19 4q21.21-21.22(chr4:82348110-83124384)x3	RASGEF1B	Copy number gain	See cases	GLikely benign

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