LOC129930994[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
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 148454	GRCh38/hg38 1p21.3(chr1:96124445-99094525)x1	DPYD, DPYD-AS1 +29 more	Copy number loss	See cases	GUncertain significance
Select item 59973	GRCh38/hg38 1p21.3(chr1:96554406-97919058)x1	DPYD, DPYD-AS1 +8 more	Copy number loss	See cases	GPathogenic

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