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

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Items: 17

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3063175	GRCh37/hg19 10q26.13-26.3(chr10:125987494-135427143)x1	ABRAXAS2, ADAM12 +55 more	Copy number loss	not specified	GPathogenic
Select item 3063168	GRCh37/hg19 10q26.2(chr10:128766924-129095479)x1	DOCK1, INSYN2A	Copy number loss	not specified	GUncertain significance
Select item 3063167	GRCh37/hg19 10q26.2(chr10:128334180-129645457)x1	DOCK1, FOXI2 +2 more	Copy number loss	not specified	GUncertain significance
Select item 3063164	GRCh37/hg19 10q23.33-26.3(chr10:95078198-135427143)x3	ABCC2, ABLIM1 +293 more	Copy number gain	not specified	GPathogenic
Select item 3063149	GRCh37/hg19 10q26.13-26.3(chr10:126127397-135427143)x1	ABRAXAS2, ADAM12 +54 more	Copy number loss	not specified	GPathogenic
Select item 3063145	GRCh37/hg19 10q26.2(chr10:128766924-128900593)x1	DOCK1	Copy number loss	not specified	GUncertain significance
Select item 1527621	GRCh37/hg19 10q26.2(chr10:128925939-128941448)	DOCK1, INSYN2A	Copy number loss	not specified	GUncertain significance
Select item 1527620	GRCh37/hg19 10q26.2(chr10:128881187-128964237)	DOCK1, INSYN2A	Copy number loss	not specified	GUncertain significance
Select item 1527619	GRCh37/hg19 10q26.2(chr10:128876823-129645457)	DOCK1, FOXI2 +2 more	Copy number loss	not specified	GUncertain significance
Select item 1527618	GRCh37/hg19 10q26.2(chr10:128766924-128898560)	DOCK1	Copy number loss	not specified	GUncertain significance
Select item 1527617	GRCh37/hg19 10q26.2(chr10:128766924-128855394)	DOCK1	Copy number loss	not specified	GUncertain significance
Select item 1527616	GRCh37/hg19 10q26.2-26.3(chr10:128465436-135427143)	ADAM8, ADGRA1 +38 more	Copy number loss	not specified	GPathogenic
Select item 1527613	GRCh37/hg19 10q26.2(chr10:128334180-128872191)	DOCK1	Copy number loss	not specified	GUncertain significance
Select item 1527612	GRCh37/hg19 10q26.2(chr10:128301285-128769606)	DOCK1	Copy number gain	not specified	GUncertain significance
Select item 1527609	GRCh37/hg19 10q26.12-26.3(chr10:122343861-135427143)	FAM24A, FAM24B +80 more	Copy number loss	not specified	GPathogenic
Select item 1527608	GRCh37/hg19 10q26.12-26.3(chr10:122125760-135062972)	ABRAXAS2, ACADSB +68 more	Copy number gain	not specified	GLikely pathogenic
Select item 1527605	GRCh37/hg19 10q25.1-26.3(chr10:108455687-135427143)	ABLIM1, ABRAXAS2 +146 more	Copy number gain	not specified	GPathogenic