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

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Items: 12

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2685162	GRCh37/hg19 5q14.3(chr5:89998097-90122803)x1	ADGRV1	Copy number loss	not provided	GUncertain significance
Select item 1809143	GRCh37/hg19 5q14.3(chr5:89869634-89956672)x1	ADGRV1	Copy number loss	not provided	GUncertain significance
Select item 1340731	GRCh37/hg19 5q14.3(chr5:90271761-90326129)x1	ADGRV1	Copy number loss	not provided	GUncertain significance
Select item 1340201	GRCh37/hg19 5q14.3(chr5:89720318-90293526)x3	ADGRV1, LYSMD3 +2 more	Copy number gain	not provided	GUncertain significance
Select item 980162	GRCh37/hg19 5q14.3(chr5:90452865-90563755)x3	ADGRV1	Copy number gain	not provided	GUncertain significance
Select item 980161	GRCh37/hg19 5q14.3(chr5:90218695-91499978)x3	ADGRV1, ARRDC3 +1 more	Copy number gain	not provided	GUncertain significance
Select item 814710	GRCh37/hg19 5q14.3(chr5:90209062-90419585)x1	ADGRV1	Copy number loss	not provided	GUncertain significance
Select item 814708	GRCh37/hg19 5q14.3(chr5:87611415-89975436)x3	MBLAC2, CETN3 +5 more	Copy number gain	not provided	GUncertain significance
Select item 814693	GRCh37/hg19 5q13.2-15(chr5:72790061-97478870)x3	ACOT12, ADGRV1 +98 more	Copy number gain	not provided	GPathogenic
Select item 563089	GRCh37/hg19 5q14.3(chr5:89998096-90138849)x1	ADGRV1	Copy number loss	not provided	GUncertain significance
Select item 563088	GRCh37/hg19 5q14.3(chr5:89864064-89889132)x1	ADGRV1	Copy number loss	not provided	GUncertain significance
Select item 563087	GRCh37/hg19 5q14.3-15(chr5:87399001-92675748)x3	ADGRV1, MIR9-2 +8 more	Copy number gain	not provided	GLikely pathogenic