"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 2685661	GRCh37/hg19 21q22.11(chr21:32528117-32806507)x1	TIAM1	Copy number loss	not provided	GUncertain significance
Select item 2684912	GRCh37/hg19 21q21.1-22.11(chr21:20408138-32852758)x3	N6AMT1, NCAM2 +52 more	Copy number gain	not provided	GPathogenic
Select item 2684910	GRCh37/hg19 21q11.2-22.3(chr21:15006458-45674637)x3	CLDN14, CLDN17 +170 more	Copy number gain	not provided	GPathogenic
Select item 1809218	GRCh37/hg19 21q22.11(chr21:32736169-33013841)x1	TIAM1	Copy number loss	not provided	GUncertain significance
Select item 1807904	GRCh37/hg19 21q22.11(chr21:32472185-32600181)x1	TIAM1	Copy number loss	not provided	GUncertain significance
Select item 1341200	GRCh37/hg19 21q11.2-22.3(chr21:15006457-48097372)x3	ABCG1, ADAMTS1 +217 more	Copy number gain	not provided	GPathogenic
Select item 1339970	GRCh37/hg19 21q22.11(chr21:32676376-35131913)x3	C21orf62, CFAP298 +24 more	Copy number gain	not provided	GUncertain significance
Select item 980233	GRCh37/hg19 21q22.11(chr21:32740461-32920742)x1	TIAM1	Copy number loss	not provided	GUncertain significance
Select item 816160	GRCh37/hg19 21q22.11(chr21:32586741-32840433)x1	TIAM1	Copy number loss	not provided	GUncertain significance
Select item 816159	GRCh37/hg19 21q22.11(chr21:31711916-34632473)x1	CFAP298, EPCIP +43 more	Copy number loss	not provided	GPathogenic