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

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2684632	GRCh37/hg19 11p15.5-15.4(chr11:192764-3362853)x3	CARS1, CD151 +89 more	Copy number gain	not provided	GPathogenic
Select item 1807629	GRCh37/hg19 11p15.5-15.4(chr11:230616-8250724)x3	CAVIN3, CCKBR +205 more	Copy number gain	not provided	GPathogenic
Select item 980951	GRCh37/hg19 11p15.5-15.4(chr11:2629917-2902668)x3	KCNQ1, KCNQ1DN +1 more	Copy number gain	not provided	GUncertain significance
Select item 980417	GRCh37/hg19 11p15.5(chr11:2585399-2669895)x1	KCNQ1, KCNQ1OT1	Copy number loss	not provided	GUncertain significance
Select item 815398	GRCh37/hg19 11p15.5-15.4(chr11:2683937-3207439)x3	CARS1, CDKN1C +8 more	Copy number gain	not provided	GUncertain significance
Select item 815397	GRCh37/hg19 11p15.5(chr11:2458744-2616835)x3	KCNQ1	Copy number gain	not provided	GUncertain significance
Select item 815396	GRCh37/hg19 11p15.5(chr11:2209396-2520511)x3	ASCL2, C11orf21 +5 more	Copy number gain	not provided	GUncertain significance
Select item 815395	GRCh37/hg19 11p15.5-13(chr11:235934-33826995)x3	CALCB, CARS1 +343 more	Copy number gain	not provided	GPathogenic
Select item 563883	GRCh37/hg19 11p15.5-15.1(chr11:230615-17099213)x3	ADM, AKIP1 +258 more	Copy number gain	not provided	GPathogenic
Select item 563880	GRCh37/hg19 11p15.5-15.4(chr11:230615-9704511)x3	AKIP1, ANO9 +222 more	Copy number gain	not provided	GPathogenic