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

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Items: 19

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1808978	GRCh37/hg19 17p12(chr17:14078283-15479940)x3	CDRT15, CDRT4 +6 more	Copy number gain	not provided	GPathogenic
Select item 1808684	GRCh37/hg19 17p12(chr17:14087934-15491532)x1	CDRT15, CDRT4 +6 more	Copy number loss	not provided	GPathogenic
Select item 1808667	GRCh37/hg19 17p12(chr17:14083055-15484859)x1	CDRT15, CDRT4 +6 more	Copy number loss	not provided	GPathogenic
Select item 1808665	GRCh37/hg19 17p12(chr17:14087934-15484358)x3	CDRT15, CDRT4 +6 more	Copy number gain	not provided	GPathogenic
Select item 1808614	GRCh37/hg19 17p12(chr17:14073563-15479923)x3	CDRT15, CDRT4 +6 more	Copy number gain	not provided	GPathogenic
Select item 1808605	GRCh37/hg19 17p12(chr17:14087934-15483608)x3	CDRT15, CDRT4 +6 more	Copy number gain	not provided	GPathogenic
Select item 1808529	GRCh37/hg19 17p12(chr17:14077819-15491532)x1	CDRT15, CDRT4 +6 more	Copy number loss	not provided	GPathogenic
Select item 1807927	GRCh37/hg19 17p12(chr17:14087788-15484858)x1	CDRT15, CDRT4 +6 more	Copy number loss	not provided	GPathogenic
Select item 1807821	GRCh37/hg19 17p12(chr17:14083055-15483608)x3	CDRT15, CDRT4 +6 more	Copy number gain	not provided	GPathogenic
Select item 1807816	GRCh37/hg19 17p12(chr17:14082945-15484858)x1	CDRT15, CDRT4 +6 more	Copy number loss	not provided	GPathogenic
Select item 1807743	GRCh37/hg19 17p12(chr17:14087934-15484630)x3	CDRT15, CDRT4 +6 more	Copy number gain	not provided	GPathogenic
Select item 1807700	GRCh37/hg19 17p12(chr17:14087934-15479940)x3	CDRT15, CDRT4 +6 more	Copy number gain	not provided	GPathogenic
Select item 1340845	GRCh37/hg19 17p12(chr17:13738798-14156469)x3	CDRT15, COX10	Copy number gain	not provided	GUncertain significance
Select item 815905	GRCh37/hg19 17p12(chr17:13933395-14055324)x1	COX10	Copy number loss	not provided	GUncertain significance
Select item 564404	GRCh37/hg19 17p12(chr17:14087933-15484858)x1	COX10, HS3ST3B1 +6 more	Copy number loss	not provided	GPathogenic
Select item 564403	GRCh37/hg19 17p12(chr17:14085652-15512120)x3	CDRT15, CDRT4 +7 more	Copy number gain	not provided	GPathogenic
Select item 564402	GRCh37/hg19 17p12(chr17:14083054-15479940)x3	HS3ST3B1, CDRT15 +6 more	Copy number gain	not provided	GPathogenic
Select item 564401	GRCh37/hg19 17p12(chr17:14076430-15491532)x3	TEKT3, CDRT4 +6 more	Copy number gain	not provided	GPathogenic
Select item 564400	GRCh37/hg19 17p12(chr17:14041216-14108096)x1	COX10	Copy number loss	not provided	GUncertain significance