"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 2685807	GRCh37/hg19 1p31.1(chr1:74993063-75580191)x3	CRYZ, ERICH3 +3 more	Copy number gain	not provided	GUncertain significance
Select item 1809024	GRCh37/hg19 1p31.1(chr1:74796513-74918340)x1	FPGT-TNNI3K, TNNI3K	Copy number loss	not provided	GUncertain significance
Select item 1808328	GRCh37/hg19 1p31.1(chr1:74734130-75521892)x3	CRYZ, ERICH3 +3 more	Copy number gain	not provided	GUncertain significance
Select item 1807962	GRCh37/hg19 1p31.1(chr1:74501101-74706387)x3	FPGT-TNNI3K, LRRIQ3 +2 more	Copy number gain	not provided	GUncertain significance
Select item 1341058	GRCh37/hg19 1p31.1(chr1:73209151-74812480)x3	FPGT, FPGT-TNNI3K +2 more	Copy number gain	not provided	GUncertain significance
Select item 1340425	GRCh37/hg19 1p31.1(chr1:74010838-74849251)x3	FPGT, FPGT-TNNI3K +2 more	Copy number gain	not provided	GUncertain significance
Select item 979896	GRCh37/hg19 1p31.1(chr1:74091361-74706387)x3	FPGT-TNNI3K, LRRIQ3 +2 more	Copy number gain	not provided	GUncertain significance
Select item 814100	GRCh37/hg19 1p31.1(chr1:74969395-75264251)x3	TNNI3K, TYW3 +3 more	Copy number gain	not provided	GUncertain significance
Select item 565113	GRCh37/hg19 1p31.1(chr1:74125095-75208561)x1	FPGT, ERICH3 +5 more	Copy number loss	not provided	GUncertain significance
Select item 565112	GRCh37/hg19 1p31.1(chr1:72859282-75395703)x3	TYW3, TNNI3K +5 more	Copy number gain	not provided	GUncertain significance
Select item 565111	GRCh37/hg19 1p31.1(chr1:72103442-77186974)x3	LRRIQ3, FPGT-TNNI3K +14 more	Copy number gain	not provided	GLikely pathogenic