"ARUP Laboratories, Cytogenetics and Genomic Microarray, ARUP Laborato - ClinVar

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Items: 28

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3063123	GRCh37/hg19 9p24.3-24.1(chr9:203862-8548307)x1	AK3, BRD10 +37 more	Copy number loss	not specified	GPathogenic
Select item 3063119	GRCh37/hg19 9p24.3(chr9:203862-328082)x1	DOCK8, DOCK8-AS1	Copy number loss	not specified	GUncertain significance
Select item 3063118	GRCh37/hg19 9p24.3(chr9:203862-265340)x1	DOCK8, DOCK8-AS1	Copy number loss	not specified	GUncertain significance
Select item 3063114	GRCh37/hg19 9p24.3(chr9:203861-268740)x1	DOCK8, DOCK8-AS1	Copy number loss	not specified	GUncertain significance
Select item 3063089	GRCh37/hg19 9p24.3-23(chr9:203861-9128400)x1	AK3, BRD10 +37 more	Copy number loss	not specified	GPathogenic
Select item 3063080	GRCh37/hg19 9p24.3-22.3(chr9:203861-15508556)x1	AK3, BRD10 +47 more	Copy number loss	not specified	GPathogenic
Select item 3063075	GRCh37/hg19 9p24.3(chr9:203861-322786)x1	DOCK8, DOCK8-AS1	Copy number loss	not specified	GUncertain significance
Select item 3063071	GRCh37/hg19 9p24.3-q34.3(chr9:203861-141020389)x3	ABCA1, ABCA2 +769 more	Copy number gain	not specified	GPathogenic
Select item 3063070	GRCh37/hg19 9p24.3-22.1(chr9:203861-19302836)x1	ADAMTSL1, AK3 +57 more	Copy number loss	not specified	GPathogenic
Select item 3063069	GRCh37/hg19 9p24.3(chr9:209753-236828)x1	DOCK8, DOCK8-AS1	Copy number loss	not specified	GUncertain significance
Select item 3063067	GRCh37/hg19 9p24.3(chr9:209753-246900)x1	DOCK8, DOCK8-AS1	Copy number loss	not specified	GPathogenic
Select item 1527491	GRCh37/hg19 9p24.3-q34.3(chr9:353349-141020389)	OR1L4, PTRH1 +768 more	Copy number gain	not specified	GPathogenic
Select item 1527490	GRCh37/hg19 9p24.3(chr9:288826-402280)	DOCK8	Copy number loss	not specified	GUncertain significance
Select item 1527489	GRCh37/hg19 9p24.3(chr9:239666-402280)	DOCK8	Copy number gain	not specified	GUncertain significance
Select item 1527488	GRCh37/hg19 9p24.3-q21.32(chr9:203861-84155399)	CDKN2B-AS1, ABHD17B +257 more	Copy number gain	not specified	GPathogenic
Select item 1527487	GRCh37/hg19 9p24.3-q21.11(chr9:203861-69002883)	ACO1, IFNA8 +205 more	Copy number gain	not specified	GPathogenic
Select item 1527485	GRCh37/hg19 9p24.3-22.2(chr9:203861-16856907)	AK3, BNC2 +49 more	Copy number loss	not specified	GPathogenic
Select item 1527484	GRCh37/hg19 9p24.3-22.3(chr9:203861-15211277)	AK3, CD274 +45 more	Copy number loss	not specified	GPathogenic
Select item 1527483	GRCh37/hg19 9p24.3-22.3(chr9:203861-14694074)	AK3, CD274 +42 more	Copy number loss	not specified	GPathogenic
Select item 1527482	GRCh37/hg19 9p24.3-22.3(chr9:203861-14322268)	AK3, CD274 +41 more	Copy number loss	not specified	GPathogenic
Select item 1527480	GRCh37/hg19 9p24.3-23(chr9:203861-11414732)	AK3, CD274 +37 more	Copy number loss	not specified	GPathogenic
Select item 1527479	GRCh37/hg19 9p24.3-23(chr9:203861-9631665)	AK3, CD274 +37 more	Copy number loss	not specified	GPathogenic
Select item 1527478	GRCh37/hg19 9p24.3-24.1(chr9:203861-8735462)	AK3, CD274 +37 more	Copy number loss	not specified	GPathogenic
Select item 1527477	GRCh37/hg19 9p24.3-24.1(chr9:203861-7759331)	AK3, CD274 +35 more	Copy number loss	not specified	GPathogenic
Select item 1527476	GRCh37/hg19 9p24.3-24.1(chr9:203861-5909152)	AK3, CD274 +28 more	Copy number loss	not specified	GPathogenic
Select item 1527475	GRCh37/hg19 9p24.3-24.2(chr9:203861-4342995)	DMRT1, DMRT2 +10 more	Copy number gain	not specified	GUncertain significance
Select item 1527474	GRCh37/hg19 9p24.3-24.2(chr9:203861-3226591)	DMRT1, DMRT2 +9 more	Copy number loss	not specified	GPathogenic
Select item 1527473	GRCh37/hg19 9p24.3(chr9:203861-268590)	DOCK8, DOCK8-AS1	Copy number loss	not specified	GUncertain significance

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Items: 28