LINC02008[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 150826	GRCh38/hg38 3p14.3-11.1(chr3:57140424-90259960)x1	ABHD6, ACOX2 +481 more	Copy number loss	See cases	GPathogenic
Select item 153529	GRCh38/hg38 3p13-11.1(chr3:73824871-90453699)x1	C3orf38, CADM2 +124 more	Copy number loss	See cases	GPathogenic
Select item 155598	GRCh38/hg38 3p12.3-11.1(chr3:74649382-89495681)x1	C3orf38, CADM2 +118 more	Copy number loss	See cases	GPathogenic
Select item 146400	GRCh38/hg38 3p12.3-11.1(chr3:76764260-89682935)x1	C3orf38, CADM2 +89 more	Copy number loss	See cases	GLikely pathogenic
Select item 145882	GRCh38/hg38 3p12.2(chr3:80214687-83388676)x3	GBE1, LINC02008 +16 more	Copy number gain	See cases	GLikely benign
Select item 57759	GRCh38/hg38 3p12.2-11.2(chr3:80320584-87468216)x3	CADM2, CADM2-AS1 +48 more	Copy number gain	See cases	GUncertain significance
Select item 57801	GRCh38/hg38 3p12.2-12.1(chr3:81504313-85127899)x1	CADM2, GBE1 +20 more	Copy number loss	See cases	GPathogenic
Select item 145220	GRCh38/hg38 3p12.2(chr3:82116407-82199434)x1	LINC02008	Copy number loss	See cases	GBenign

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