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

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Items: 13

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2684658	GRCh37/hg19 11q24.2(chr11:126660043-127714651)x3	KIRREL3, LOC101929473	Copy number gain	not provided	GUncertain significance
Select item 1809172	GRCh37/hg19 11q24.2(chr11:125812020-126308722)x3	RPUSD4, SRPRA +7 more	Copy number gain	not provided	GUncertain significance
Select item 1808652	GRCh37/hg19 11q24.1-25(chr11:122975824-134938470)x1	ACAD8, ACRV1 +94 more	Copy number loss	not provided	GPathogenic
Select item 1808248	GRCh37/hg19 11q24.2(chr11:126100551-126437941)x3	DCPS, FAM118B +5 more	Copy number gain	not provided	GUncertain significance
Select item 1341168	GRCh37/hg19 11q23.1-24.3(chr11:112375478-128785742)x3	ABCG4, ACRV1 +172 more	Copy number gain	not provided	GPathogenic
Select item 1341131	GRCh37/hg19 11q24.2(chr11:126462437-126678981)x3	KIRREL3	Copy number gain	not provided	GUncertain significance
Select item 979328	GRCh37/hg19 11q24.2-25(chr11:125785487-134938470)x1	TP53AIP1, FLI1 +41 more	Copy number loss	not provided	GPathogenic
Select item 815481	GRCh37/hg19 11q24.2(chr11:126734337-126944508)x3	LOC101929473, KIRREL3	Copy number gain	not provided	GUncertain significance
Select item 815480	GRCh37/hg19 11q24.2(chr11:126201307-126466438)x3	KIRREL3, ST3GAL4 +1 more	Copy number gain	not provided	GUncertain significance
Select item 815477	GRCh37/hg19 11q24.2-25(chr11:124232608-134938470)x1	LINC02743, VSIG2 +74 more	Copy number loss	not provided	GPathogenic
Select item 815475	GRCh37/hg19 11q23.3-25(chr11:120742540-134938470)x1	ACAD8, ACRV1 +108 more	Copy number loss	not provided	GPathogenic
Select item 563884	GRCh37/hg19 11q23.3-25(chr11:116681007-134938470)x3	ABCG4, ACAD8 +177 more	Copy number gain	not provided	GPathogenic
Select item 563882	GRCh37/hg19 11q23.3-25(chr11:119538664-134938470)x1	ACAD8, ACRV1 +114 more	Copy number loss	not provided	GPathogenic