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

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3063427	GRCh37/hg19 16p13.3-13.2(chr16:6144666-8016946)x1	RBFOX1	Copy number loss	not specified	GUncertain significance
Select item 3063420	GRCh37/hg19 16p13.3(chr16:6782302-7123713)x1	RBFOX1	Copy number loss	not specified	GUncertain significance
Select item 1526491	GRCh37/hg19 16p13.3(chr16:7595194-7693276)	RBFOX1	Copy number loss	not specified	GUncertain significance
Select item 1526490	GRCh37/hg19 16p13.3(chr16:7569394-7708073)	RBFOX1	Copy number loss	not specified	GUncertain significance
Select item 1526489	GRCh37/hg19 16p13.3(chr16:7034267-7143879)	RBFOX1	Copy number loss	not specified	GUncertain significance
Select item 1526488	GRCh37/hg19 16p13.3(chr16:6958175-7441851)	RBFOX1	Copy number loss	not specified	GUncertain significance
Select item 1526487	GRCh37/hg19 16p13.3(chr16:6641924-6791692)	RBFOX1	Copy number loss	not specified	GUncertain significance
Select item 1526486	GRCh37/hg19 16p13.3(chr16:6302520-6398142)	RBFOX1	Copy number loss	not specified	GUncertain significance

ClinVar