Related gene-specific medical variations for Gene (Select 10656) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2685324	GRCh37/hg19 8q24.22-24.23(chr8:135860037-138727091)x1	KHDRBS3	Copy number loss	not provided	GUncertain significance
Select item 979855	GRCh37/hg19 8q24.23(chr8:136448455-137011634)x3	KHDRBS3	Copy number gain	not provided	GLikely benign
Select item 563526	GRCh37/hg19 8q24.23(chr8:136482322-138418828)x3	KHDRBS3	Copy number gain	not provided	GLikely benign
Select item 443175	GRCh37/hg19 8q24.22-24.23(chr8:136253772-136944174)x3	KHDRBS3	Copy number gain	See cases	GUncertain significance

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