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

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Items: 13

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2685967	GRCh37/hg19 4q11-12(chr4:52685980-54252935)x3	DANCR, DCUN1D4 +10 more	Copy number gain	not provided	GUncertain significance
Select item 2685108	GRCh37/hg19 4q11-13.1(chr4:52685685-61903883)x1	AASDH, ARL9 +36 more	Copy number loss	not provided	GPathogenic
Select item 1809499	GRCh37/hg19 4q12(chr4:53434611-54079547)x3	DANCR, ERVMER34-1 +5 more	Copy number gain	not provided	GUncertain significance
Select item 1809000	GRCh37/hg19 4q12(chr4:53098544-53949065)x1	DANCR, ERVMER34-1 +5 more	Copy number loss	not provided	GUncertain significance
Select item 1808462	GRCh37/hg19 4q11-12(chr4:52685980-59272025)x3	AASDH, ARL9 +36 more	Copy number gain	not provided	GUncertain significance
Select item 1808351	GRCh37/hg19 4q12(chr4:54169393-54283313)x1	FIP1L1, SCFD2	Copy number loss	not provided	GUncertain significance
Select item 1808350	GRCh37/hg19 4q12(chr4:53715514-53925549)x1	RASL11B, SCFD2	Copy number loss	not provided	GUncertain significance
Select item 1808055	GRCh37/hg19 4q12(chr4:54228585-54361640)x1	FIP1L1, LNX1 +1 more	Copy number loss	not provided	GUncertain significance
Select item 1340920	GRCh37/hg19 4q11-12(chr4:52685685-58104722)x1	AASDH, ARL9 +36 more	Copy number loss	not provided	GPathogenic
Select item 1340288	GRCh37/hg19 4q12-31.21(chr4:52866944-143582507)x3	AASDH, ABCG2 +359 more	Copy number gain	not provided	GPathogenic
Select item 814553	GRCh37/hg19 4q12(chr4:54139333-54203666)x1	SCFD2	Copy number loss	not provided	GUncertain significance
Select item 814552	GRCh37/hg19 4q12(chr4:53688710-54741991)x3	SCFD2, FIP1L1 +2 more	Copy number gain	not provided	GUncertain significance
Select item 562913	GRCh37/hg19 4q12(chr4:53961609-54067101)x1	SCFD2	Copy number loss	not provided	GUncertain significance