Related gene-specific medical variations for Gene (Select 1007) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1341059	GRCh37/hg19 5p14.1(chr5:26761647-27436994)x3	CDH9	Copy number gain	not provided	GLikely benign
Select item 814677	GRCh37/hg19 5p14.1(chr5:26993898-27072933)x1	CDH9	Copy number loss	not provided	GUncertain significance
Select item 685204	GRCh37/hg19 5p14.1(chr5:26761647-27473808)x3	CDH9	Copy number gain	not provided	GUncertain significance
Select item 443442	GRCh37/hg19 5p14.1(chr5:26626793-27280999)x1	CDH9	Copy number loss	See cases	GUncertain significance
Select item 442697	GRCh37/hg19 5p14.1(chr5:26785032-27996752)x1	CDH9	Copy number loss	See cases	GUncertain significance
Select item 91992	NM_016279.4(CDH9):c.2202G>A (p.Ser734=)	CDH9	Single nucleotide variant (synonymous variant)	not provided	GUncertain significance

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