Related gene-specific medical variations for Gene (Select 8821) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 980141	GRCh37/hg19 4q31.21(chr4:143113600-144098686)x3	INPP4B	Copy number gain	not provided	GLikely benign
Select item 524175	t(4;16)(q31;q13)dn	INPP4B	Translocation	not specified	GUncertain significance
Select item 394191	GRCh37/hg19 4q31.21(chr4:143733281-144002697)x3	INPP4B	Copy number gain	See cases	GLikely benign
Select item 394067	GRCh37/hg19 4q31.21(chr4:143086405-143195842)x3	INPP4B	Copy number gain	See cases	GBenign

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