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

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1809011	GRCh37/hg19 3p14.1(chr3:65489460-65780869)x1	MAGI1	Copy number loss	not provided	GUncertain significance
Select item 1808122	GRCh37/hg19 3p14.1(chr3:65448162-67283742)x3	KBTBD8, LRIG1 +1 more	Copy number gain	not provided	GUncertain significance
Select item 1341307	GRCh37/hg19 3p14.2-13(chr3:59332508-70686155)x1	ADAMTS9, ARL6IP5 +24 more	Copy number loss	not provided	GPathogenic
Select item 1340768	GRCh37/hg19 3p14.1(chr3:65557424-65753176)x1	MAGI1	Copy number loss	not provided	GUncertain significance
Select item 814451	GRCh37/hg19 3p14.1(chr3:65459431-67283891)x3	MAGI1, KBTBD8 +1 more	Copy number gain	not provided	GUncertain significance
Select item 814449	GRCh37/hg19 3p14.2-14.1(chr3:60449667-65561638)x1	SYNPR, ATXN7 +11 more	Copy number loss	not provided	GPathogenic
Select item 562780	GRCh37/hg19 3p14.1(chr3:65609952-65661896)x1	MAGI1	Copy number loss	not provided	GLikely benign
Select item 562779	GRCh37/hg19 3p14.1(chr3:65502771-66378999)x3	MAGI1	Copy number gain	not provided	GUncertain significance
Select item 562778	GRCh37/hg19 3p14.1(chr3:65448161-67286083)x3	KBTBD8, MAGI1 +1 more	Copy number gain	not provided	GUncertain significance

ClinVar