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

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1809255	GRCh37/hg19 4q21.21(chr4:78947327-79326031)x1	FRAS1	Copy number loss	not provided	GUncertain significance
Select item 1340288	GRCh37/hg19 4q12-31.21(chr4:52866944-143582507)x3	AASDH, ABCG2 +359 more	Copy number gain	not provided	GPathogenic
Select item 814573	GRCh37/hg19 4q21.21(chr4:79112309-79175262)x1	FRAS1	Copy number loss	not provided	GUncertain significance
Select item 814572	GRCh37/hg19 4q21.1-21.21(chr4:78780969-79455176)x3	FRAS1, MRPL1	Copy number gain	not provided	GLikely benign
Select item 814566	GRCh37/hg19 4q13.3-21.23(chr4:72680879-86426232)x1	CXCL3, LIN54 +82 more	Copy number loss	not provided	GPathogenic
Select item 814563	GRCh37/hg19 4q13.2-21.21(chr4:68950363-79738598)x1	ADAMTS3, AFM +92 more	Copy number loss	not provided	GPathogenic
Select item 562935	GRCh37/hg19 4q21.21(chr4:79256988-81081299)x1	BMP2K, ANXA3 +6 more	Copy number loss	not provided	GUncertain significance

ClinVar