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

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2685602	GRCh37/hg19 17q21.31(chr17:44135737-44212416)x1	KANSL1	Copy number loss	not provided	GLikely pathogenic
Select item 2684850	GRCh37/hg19 17q21.31(chr17:44079186-44228987)x3	KANSL1, MAPT	Copy number gain	not provided	GUncertain significance
Select item 1809344	GRCh37/hg19 17q21.31(chr17:43693538-44212416)x1	CRHR1, KANSL1 +3 more	Copy number loss	not provided	GPathogenic
Select item 1808674	GRCh37/hg19 17q21.31(chr17:43622197-44212416)x1	CRHR1, KANSL1 +3 more	Copy number loss	not provided	GPathogenic
Select item 980719	GRCh37/hg19 17q21.31(chr17:43586396-44212416)x1	CRHR1, KANSL1 +3 more	Copy number loss	not provided	GPathogenic
Select item 815938	GRCh37/hg19 17q21.31(chr17:43655356-44784639)x3	ARL17A, ARL17B +8 more	Copy number gain	not provided	GPathogenic
Select item 564449	GRCh37/hg19 17q21.31(chr17:43703800-44212416)x1	KANSL1, STH +3 more	Copy number loss	not provided	GPathogenic
Select item 564448	GRCh37/hg19 17q21.31(chr17:43688308-44163085)x1	MAPT, KANSL1 +3 more	Copy number loss	not provided	GPathogenic

ClinVar