"ARUP Laboratories, Cytogenetics and Genomic Microarray, ARUP Laborato - ClinVar

Format

Sort by

Choose Destination

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3063499	GRCh37/hg19 1q44(chr1:246179295-246704479)x1	SMYD3, TFB2M	Copy number loss	not specified	GUncertain significance
Select item 3063133	GRCh37/hg19 1q43-44(chr1:238681812-249224684)x3	OR2W3, OR6F1 +81 more	Copy number gain	not specified	GLikely pathogenic
Select item 3062700	GRCh37/hg19 1q44(chr1:244579324-246515944)x1	ADSS2, CATSPERE +6 more	Copy number loss	not specified	GPathogenic
Select item 1527714	GRCh37/hg19 1q44(chr1:246109449-246595110)	SMYD3	Copy number gain	not specified	GUncertain significance

Format

Sort by

Choose Destination

ClinVar