Related gene-specific medical variations for Gene (Select 168975) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 979840	GRCh37/hg19 8q21.3(chr8:88257878-88328681)x1	CNBD1	Copy number loss	not provided	GLikely benign
Select item 815143	GRCh37/hg19 8q21.3(chr8:88389021-88440493)x1	CNBD1	Copy number loss	not provided	GLikely benign
Select item 688126	GRCh37/hg19 8q21.3(chr8:87982773-88732332)x4	CNBD1	Copy number gain	not provided	GUncertain significance
Select item 563426	GRCh37/hg19 8q21.3(chr8:87868805-87942903)x1	CNBD1	Copy number loss	not provided	GUncertain significance
Select item 394451	GRCh37/hg19 8q21.3(chr8:87991948-88103660)x1	CNBD1	Copy number loss	See cases	GLikely benign
Select item 153909	GRCh38/hg38 8q21.3(chr8:87104001-87352530)x1	CNBD1	Copy number loss	See cases	GUncertain significance
Select item 152007	GRCh38/hg38 8q21.3(chr8:87031681-87243497)x1	CNBD1	Copy number loss	See cases	GLikely benign

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