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

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Items: 11

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2684860	GRCh37/hg19 17q25.3(chr17:80678790-80943685)x3	B3GNTL1, FN3K +3 more	Copy number gain	not provided	GUncertain significance
Select item 1808859	GRCh37/hg19 17q25.3(chr17:80809608-81041938)x3	B3GNTL1, METRNL +1 more	Copy number gain	not provided	GUncertain significance
Select item 1808572	GRCh37/hg19 17q25.3(chr17:80585033-81041938)x3	B3GNTL1, FN3K +6 more	Copy number gain	not provided	GUncertain significance
Select item 1340721	GRCh37/hg19 17q25.3(chr17:80555363-81041938)x1	B3GNTL1, FN3K +7 more	Copy number loss	not provided	GUncertain significance
Select item 1340696	GRCh37/hg19 17q25.3(chr17:80787030-81041938)x3	B3GNTL1, METRNL +2 more	Copy number gain	not provided	GUncertain significance
Select item 815956	GRCh37/hg19 17q25.3(chr17:80717487-81041938)x3	TBCD, B3GNTL1 +2 more	Copy number gain	not provided	GUncertain significance
Select item 564481	GRCh37/hg19 17q25.3(chr17:80759659-80876866)x1	TBCD, ZNF750	Copy number loss	not provided	GUncertain significance
Select item 564480	GRCh37/hg19 17q25.3(chr17:80555321-81041938)x1	B3GNTL1, FN3K +7 more	Copy number loss	not provided	GUncertain significance
Select item 564479	GRCh37/hg19 17q25.3(chr17:80489175-81041938)x1	ZNF750, TBCD +7 more	Copy number loss	not provided	GUncertain significance
Select item 564476	GRCh37/hg19 17q25.3(chr17:76552611-81041938)x3	AATK, ACTG1 +88 more	Copy number gain	not provided	GLikely pathogenic
Select item 564463	GRCh37/hg19 17q24.1-25.3(chr17:63689671-81041938)x3	AANAT, AATK +222 more	Copy number gain	not provided	GPathogenic