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

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Search results

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2685086	GRCh37/hg19 3p12.2(chr3:81531796-81707690)x1	GBE1	Copy number loss	not provided	GUncertain significance
Select item 1808015	GRCh37/hg19 3p12.2-12.1(chr3:80726890-83949110)x1	GBE1	Copy number loss	not provided	GUncertain significance
Select item 1341146	GRCh37/hg19 3p12.2(chr3:81778755-81853384)x1	GBE1	Copy number loss	not provided	GUncertain significance
Select item 980023	GRCh37/hg19 3p12.2-12.1(chr3:80873527-85127795)x3	GBE1, CADM2	Copy number gain	not provided	GUncertain significance
Select item 980022	GRCh37/hg19 3p12.2(chr3:81540099-81597277)x1	GBE1	Copy number loss	not provided	GUncertain significance
Select item 814459	GRCh37/hg19 3p12.2(chr3:81255104-81637659)x4	GBE1	Copy number gain	not provided	GUncertain significance
Select item 562789	GRCh37/hg19 3p12.2(chr3:81697485-83389064)x3	GBE1	Copy number gain	not provided	GUncertain significance
Select item 562788	GRCh37/hg19 3p12.2(chr3:81675729-82141036)x3	GBE1	Copy number gain	not provided	GUncertain significance
Select item 562787	GRCh37/hg19 3p12.2(chr3:81586741-81735611)x1	GBE1	Copy number loss	not provided	GUncertain significance
Select item 562786	GRCh37/hg19 3p12.2(chr3:80247482-83468911)x3	GBE1	Copy number gain	not provided	GUncertain significance