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

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Items: 5

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3062981	GRCh37/hg19 7p14.3-14.1(chr7:33478398-39686397)x1	AMPH, ANLN +22 more	Copy number loss	not specified	GLikely pathogenic
Select item 3062965	GRCh37/hg19 7p14.3(chr7:33293316-33347833)x1	BBS9	Copy number loss	not specified	GUncertain significance
Select item 1527347	GRCh37/hg19 7p14.3(chr7:33224145-33642387)	BBS9	Copy number loss	not specified	GUncertain significance
Select item 1527345	GRCh37/hg19 7p15.2-14.1(chr7:27507832-39072473)	ADCYAP1R1, AMPH +53 more	Copy number gain	not specified	GLikely pathogenic
Select item 1527336	GRCh37/hg19 7p21.3-14.2(chr7:10745750-35305167)	ABCB5, ADCYAP1R1 +117 more	Copy number gain	not specified	GLikely pathogenic

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