ClinVar for Gene (Select 126859700) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
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 144743	GRCh38/hg38 6q11.1-12(chr6:61468685-63437335)x1	FKBP1C, KHDRBS2 +14 more	Copy number loss	See cases	GUncertain significance

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