Related gene-specific medical variations for Gene (Select 157697) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 815069	GRCh37/hg19 8p23.3(chr8:639795-1275384)x3	ERICH1	Copy number gain	not provided	GLikely benign
Select item 815068	GRCh37/hg19 8p23.3(chr8:541616-853721)x3	ERICH1	Copy number gain	not provided	GLikely benign
Select item 688616	GRCh37/hg19 8p23.3(chr8:627180-768460)x1	ERICH1	Copy number loss	not provided	GUncertain significance
Select item 687785	GRCh37/hg19 8p23.3(chr8:541616-723786)x3	ERICH1	Copy number gain	not provided	GUncertain significance
Select item 686765	GRCh37/hg19 8p23.3(chr8:504901-983722)x3	ERICH1	Copy number gain	not provided	GUncertain significance
Select item 686558	GRCh37/hg19 8p23.3(chr8:635033-859851)x1	ERICH1	Copy number loss	not provided	GUncertain significance
Select item 563512	GRCh37/hg19 8p23.3(chr8:541616-1368583)x3	ERICH1	Copy number gain	not provided	GLikely benign
Select item 441730	GRCh37/hg19 8p23.3(chr8:541616-1058714)x3	ERICH1	Copy number gain	See cases	GLikely benign
Select item 394459	GRCh37/hg19 8p23.3(chr8:614223-665873)x1	ERICH1	Copy number loss	See cases	GUncertain significance

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