ClinVar for dbVar (Select 48488155) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 160908	GRCh38/hg38 16p12.2(chr16:21826171-22396610)x1	CDR2, CDR2-DT +36 more	Copy number loss	See cases	GUncertain significance
Select item 34545	GRCh38/hg38 16p12.2(chr16:21826171-22396610)x3	CDR2, CDR2-DT +36 more	Copy number gain	See cases	GUncertain significance
Select item 32255	GRCh38/hg38 16p12.2(chr16:21826171-22396610)x1	CDR2, CDR2-DT +36 more	Copy number loss	See cases	GUncertain significance; Pathogenic/Likely pathogenic

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