ClinVar for Gene (Select 100873933) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 148454	GRCh38/hg38 1p21.3(chr1:96124445-99094525)x1	DPYD, DPYD-AS1 +29 more	Copy number loss	See cases	GUncertain significance
Select item 146496	GRCh38/hg38 1p21.3(chr1:97200180-97877546)x1	DPYD, DPYD-AS1 +2 more	Copy number loss	See cases	GBenign
Select item 146350	GRCh38/hg38 1p31.1-21.1(chr1:83457325-104273917)x3	LINC01708, LINC01709 +549 more	Copy number gain	See cases	GPathogenic
Select item 146007	GRCh38/hg38 1p21.3-13.3(chr1:97272349-108893138)x1	AGL, AKNAD1 +195 more	Copy number loss	See cases	GPathogenic
Select item 60005	GRCh38/hg38 1p21.3-13.3(chr1:97410602-110670510)x1	AGL, AHCYL1 +333 more	Copy number loss	See cases	GPathogenic
Select item 59973	GRCh38/hg38 1p21.3(chr1:96554406-97919058)x1	DPYD, DPYD-AS1 +8 more	Copy number loss	See cases	GPathogenic
Select item 57787	GRCh38/hg38 1p21.3(chr1:97417705-97919058)x3	DPYD, DPYD-AS2 +1 more	Copy number gain	See cases	GUncertain significance

ClinVar