"Quest Diagnostics Nichols Institute San Juan Capistrano"[submitter] A - ClinVar

Format

Sort by

Choose Destination

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1340750	GRCh37/hg19 3p22.1(chr3:42182456-42235006)x1	TRAK1	Copy number loss	not provided	GUncertain significance
Select item 980512	GRCh37/hg19 3p22.1(chr3:42008472-42610176)x3	LYZL4, SEC22C +3 more	Copy number gain	not provided	GUncertain significance
Select item 980511	GRCh37/hg19 3p22.1(chr3:41917315-42217850)x3	ULK4, TRAK1	Copy number gain	not provided	GLikely benign
Select item 562760	GRCh37/hg19 3p24.3-21.31(chr3:16923595-45249923)x2,3	ABHD5, ACAA1 +135 more	Copy number gain	not provided	GPathogenic

Format

Sort by

Choose Destination

ClinVar