Related gene-specific medical variations for Gene (Select 2687) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 395299	GRCh37/hg19 22q11.23(chr22:24640758-24658665)x3	GGT5	Copy number gain	See cases	GLikely benign
Select item 394803	GRCh37/hg19 22q11.23(chr22:24622697-24658565)x3	GGT5	Copy number gain	See cases	GLikely benign
Select item 393735	GRCh37/hg19 22q11.23(chr22:24640758-24658565)x3	GGT5	Copy number gain	See cases	GBenign/Likely benign

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