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

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1807968	GRCh37/hg19 10q25.1(chr10:108528839-108639896)x1	SORCS1	Copy number loss	not provided	GUncertain significance
Select item 1340153	GRCh37/hg19 10q25.1-25.3(chr10:107092654-117852548)x1	ABLIM1, ACSL5 +32 more	Copy number loss	not provided	GUncertain significance
Select item 815378	GRCh37/hg19 10q25.1(chr10:108254463-110095168)x1	SORCS1	Copy number loss	not provided	GUncertain significance
Select item 815377	GRCh37/hg19 10q25.1(chr10:107728409-109787853)x3	SORCS1	Copy number gain	not provided	GUncertain significance
Select item 563802	GRCh37/hg19 10q23.33-26.3(chr10:94346520-135427143)x3	ABCC2, ABLIM1 +298 more	Copy number gain	not provided	GPathogenic
Select item 563801	GRCh37/hg19 10q24.33-26.3(chr10:105613040-135427143)x3	ABLIM1, ABRAXAS2 +157 more	Copy number gain	not provided	GPathogenic
Select item 563784	GRCh37/hg19 10q25.1(chr10:108777825-111742179)x1	SORCS1, XPNPEP1	Copy number loss	not provided	GUncertain significance
Select item 563783	GRCh37/hg19 10q25.1(chr10:108496654-111204450)x3	SORCS1	Copy number gain	not provided	GUncertain significance

ClinVar