ClinVar for Gene (Select 126088089) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 150481	GRCh38/hg38 6q11.1(chr6:60452042-60679145)x3	LOC126088089, LOC126088090	Copy number gain	See cases	GLikely benign
Select item 148991	GRCh38/hg38 6p11.2-q12(chr6:57466921-68712228)x3	ADGRB3, ADGRB3-DT +105 more	Copy number gain	See cases	GPathogenic
Select item 148002	GRCh38/hg38 6p12.1-q12(chr6:53931543-68149750)x3	BAG2, BEND6 +147 more	Copy number gain	See cases	GPathogenic
Select item 147697	GRCh38/hg38 6p11.2-q11.1(chr6:57788605-62177316)x3	KHDRBS2, LINC00680 +16 more	Copy number gain	See cases	GBenign
Select item 145766	GRCh38/hg38 6p11.2-q11.1(chr6:57788605-61701905)x3	KHDRBS2, LINC00680 +16 more	Copy number gain	See cases	GBenign
Select item 144898	GRCh38/hg38 6q11.1(chr6:60388301-60706083)x3	LOC123744832, LOC126088089 +1 more	Copy number gain	See cases	GBenign

ClinVar