LINC01149[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 155430	GRCh38/hg38 6p25.3-12.3(chr6:156974-46789291)x3	ILRUN-AS1, IP6K3 +2582 more	Copy number gain	See cases	GPathogenic
Select item 157007	NR_002812.3(HCG26):n.-83887_14635dup	HCG26, HCP5 +5 more	Duplication	Preeclampsia	Gnot provided
Select item 147104	GRCh38/hg38 6p21.33(chr6:31413982-31477904)x1	HCG26, HCP5 +3 more	Copy number loss	See cases	GBenign

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