LINC00960[gene] - ClinVar - NCBI

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Items: 12

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 150826	GRCh38/hg38 3p14.3-11.1(chr3:57140424-90259960)x1	HTD2, HTR1F +482 more	Copy number loss	See cases	GPathogenic
Select item 57772	GRCh38/hg38 3p14.1-12.3(chr3:64761248-78410098)x1	ADAMTS9-AS2, ARL6IP5 +234 more	Copy number loss	See cases	GPathogenic
Select item 151504	GRCh38/hg38 3p14.1-12.3(chr3:68328980-76764319)x3	ARL6IP5, CNTN3 +175 more	Copy number gain	See cases	GLikely pathogenic
Select item 153529	GRCh38/hg38 3p13-11.1(chr3:73824871-90453699)x1	C3orf38, CADM2 +124 more	Copy number loss	See cases	GPathogenic
Select item 155598	GRCh38/hg38 3p12.3-11.1(chr3:74649382-89495681)x1	C3orf38, CADM2 +118 more	Copy number loss	See cases	GPathogenic
Select item 154281	GRCh38/hg38 3p12.3(chr3:75153221-76021659)x3	FRG2C, LINC00960 +17 more	Copy number gain	See cases	GLikely benign
Select item 156869	NR_031714.1(MIR1324):n.-251239_47012del	LOC129937069, LOC129937070 +8 more	Deletion	Preeclampsia +2 more	Gnot provided
Select item 149648	GRCh38/hg38 3p12.3(chr3:75422685-75744282)x1	LOC129937069, FRG2C +11 more	Copy number loss	See cases	GLikely benign
Select item 147855	GRCh38/hg38 3p12.3(chr3:75522003-75744122)x1	FRG2C, LINC00960 +5 more	Copy number loss	See cases	GBenign
Select item 152484	GRCh38/hg38 3p12.3(chr3:75654754-75742414)x3	FRG2C, LINC00960 +3 more	Copy number gain	See cases	GBenign
Select item 152464	GRCh38/hg38 3p12.3(chr3:75654754-75814049)x3	FRG2C, LINC00960 +5 more	Copy number gain	See cases	GBenign
Select item 152485	GRCh38/hg38 3p12.3(chr3:75669377-75742414)x3	LINC00960, LOC123002306 +2 more	Copy number gain	See cases	GBenign