Related gene-specific medical variations for Gene (Select 1006) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1807665	GRCh37/hg19 16q21(chr16:61294662-61895318)x3	CDH8	Copy number gain	not provided	GUncertain significance
Select item 1526513	GRCh37/hg19 16q21(chr16:61740732-62068670)	CDH8	Copy number loss	not specified	GUncertain significance
Select item 1340012	GRCh37/hg19 16q21(chr16:61943832-62624292)x1	CDH8	Copy number loss	not provided	GUncertain significance
Select item 931967	NM_001796.5(CDH8):c.749G>A (p.Gly250Asp)	CDH8 (G250D)	Single nucleotide variant (missense variant)	See cases	GUncertain significance
Select item 686504	GRCh37/hg19 16q21(chr16:61842331-61951591)x3	CDH8	Copy number gain	not provided	GUncertain significance
Select item 443230	GRCh37/hg19 16q21(chr16:61491753-61868752)x3	CDH8	Copy number gain	See cases	GLikely benign
Select item 441723	GRCh37/hg19 16q21(chr16:61491418-61868752)x3	CDH8	Copy number gain	See cases	GLikely benign
Select item 253842	GRCh37/hg19 16q21(chr16:61828999-61962694)x3	CDH8	Copy number gain	See cases	GUncertain significance
Select item 155614	GRCh38/hg38 16q21(chr16:61782048-61799470)x1	CDH8	Copy number loss	See cases	GUncertain significance

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