LINC01487[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 145614	GRCh38/hg38 3q13.11-29(chr3:103426882-198110178)x3	BPESC1, BTLA +2645 more	Copy number gain	See cases	GPathogenic
Select item 57982	GRCh38/hg38 3q24-26.32(chr3:147442566-178522531)x3	LOC129937944, LOC129937945 +630 more	Copy number gain	See cases	GPathogenic
Select item 57983	GRCh38/hg38 3q24-29(chr3:147521892-198096565)x3	BDH1, C3orf33 +1449 more	Copy number gain	See cases	GPathogenic
Select item 150609	GRCh38/hg38 3q25.1-29(chr3:152100512-198118383)x3	LINC00578, LINC00880 +1317 more	Copy number gain	See cases	GPathogenic
Select item 147778	GRCh38/hg38 3q25.2(chr3:154817795-155269377)x1	LINC01487, LOC121725159 +4 more	Copy number loss	See cases	GUncertain significance
Select item 60122	GRCh38/hg38 3q25.2(chr3:154843789-155242564)x1	LINC01487, LOC121725159 +4 more	Copy number loss	See cases	GUncertain significance
Select item 60123	GRCh38/hg38 3q25.2-25.31(chr3:154870557-155444826)x1	LINC01487, LOC121725159 +6 more	Copy number loss	See cases	GUncertain significance

ClinVar