"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 3063471	GRCh37/hg19 16q24.3(chr16:89462287-89526985)x1	ANKRD11, LOC101927817	Copy number loss	not specified	GPathogenic
Select item 3063464	GRCh37/hg19 16q24.3(chr16:89472880-89612756)x1	ANKRD11, LOC101927817 +1 more	Copy number loss	not specified	GPathogenic
Select item 3063429	GRCh37/hg19 16q24.3(chr16:89127212-89339094)x3	ACSF3, ANKRD11 +3 more	Copy number gain	not specified	GUncertain significance
Select item 3063426	GRCh37/hg19 16q24.3(chr16:89151360-89518831)x1	ACSF3, ANKRD11 +4 more	Copy number loss	not specified	GPathogenic
Select item 3063398	GRCh37/hg19 16q24.3(chr16:89462287-89772750)x3	ANKRD11, CDK10 +8 more	Copy number gain	not specified	GUncertain significance
Select item 3063397	GRCh37/hg19 16q24.3(chr16:89505521-89592077)x1	ANKRD11, LOC101927817 +1 more	Copy number loss	not specified	GPathogenic
Select item 1526555	GRCh37/hg19 16q24.3(chr16:89532003-89570635)	ANKRD11	Copy number loss	not specified	GPathogenic
Select item 1526554	GRCh37/hg19 16q24.3(chr16:89505328-89561269)	ANKRD11, LOC101927817	Copy number loss	not specified	GPathogenic
Select item 1526553	GRCh37/hg19 16q24.3(chr16:89462149-89552342)	ANKRD11, LOC101927817	Copy number loss	not specified	GPathogenic
Select item 1526551	GRCh37/hg19 16q24.3(chr16:89434509-89490401)	ANKRD11	Copy number loss	not specified	GPathogenic
Select item 1526550	GRCh37/hg19 16q24.3(chr16:89430010-89601261)	ANKRD11, LOC101927817 +1 more	Copy number loss	not specified	GPathogenic
Select item 1526549	GRCh37/hg19 16q24.3(chr16:89342189-89428443)	ANKRD11	Copy number loss	not specified	GPathogenic
Select item 1526548	GRCh37/hg19 16q24.3(chr16:89296939-89420254)	ANKRD11	Copy number loss	not specified	GPathogenic
Select item 1526547	GRCh37/hg19 16q24.3(chr16:89273377-89592077)	ANKRD11, LOC101927817 +2 more	Copy number gain	not specified	GUncertain significance
Select item 1526546	GRCh37/hg19 16q24.3(chr16:89270491-89393840)	ANKRD11, ZNF778	Copy number loss	not specified	GPathogenic
Select item 1526545	GRCh37/hg19 16q24.3(chr16:88985997-89962916)	ACSF3, ANKRD11 +18 more	Copy number gain	not specified	GUncertain significance
Select item 1526543	GRCh37/hg19 16q24.3(chr16:88801603-89509853)	ACSF3, ANKRD11 +11 more	Copy number gain	not specified	GUncertain significance