ARL5B[gene] - ClinVar

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Items: 26

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 155636	GRCh38/hg38 10p15.3-12.31(chr10:54086-19336980)x1	PROSER2-AS1, PRPF18 +680 more	Copy number loss	See cases	GPathogenic
Select item 59657	GRCh38/hg38 10p15.3-12.31(chr10:69261-19184047)x3	LOC126860819, LOC126860820 +680 more	Copy number gain	See cases	GPathogenic
Select item 149407	GRCh38/hg38 10p15.3-12.1(chr10:90205-26339978)x3	ACBD7, ACBD7-DCLRE1CP1 +837 more	Copy number gain	See cases	GPathogenic
Select item 152998	GRCh38/hg38 10p15.1-q11.22(chr10:4604734-48074662)x3	ABI1, ACBD5 +1221 more	Copy number gain	See cases	GBenign
Select item 148232	GRCh38/hg38 10p14-12.31(chr10:7428770-21587752)x1	ACBD7, ACBD7-DCLRE1CP1 +388 more	Copy number loss	See cases	GPathogenic
Select item 57884	GRCh38/hg38 10p12.33-12.31(chr10:18289967-19647340)x3	ARL5B, CACNB2 +10 more	Copy number gain	See cases	GUncertain significance
Select item 2257888	NM_178815.5(ARL5B):c.202G>A (p.Gly68Ser)	ARL5B (G68S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2372930	NM_178815.5(ARL5B):c.226T>G (p.Ser76Ala)	ARL5B (S76A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3129562	NM_178815.5(ARL5B):c.385A>T (p.Met129Leu)	ARL5B (M129L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3129563	NM_178815.5(ARL5B):c.524G>A (p.Arg175Gln)	ARL5B (R175Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2684599	GRCh37/hg19 10p12.32-12.31(chr10:18690973-18976780)x3	ARL5B, CACNB2 +1 more	Copy number gain	not provided	GUncertain significance
Select item 2574696	GRCh37/hg19 10p14-q26.3(chr10:11138692-135427143)	AGAP5, CRTAC1 +682 more	Copy number gain	Distal trisomy 10q	GPathogenic
Select item 2574686	GRCh37/hg19 10p13-q26.3(chr10:12829206-135427143)	ABRAXAS2, CHCHD1 +673 more	Copy number loss	Distal 10q deletion syndrome	GPathogenic
Select item 1527577	GRCh37/hg19 10p15.1-11.21(chr10:6273934-34732521)	ABI1, ACBD5 +111 more	Copy number gain	not specified	GPathogenic
Select item 1339781	GRCh37/hg19 10p15.3-q11.22(chr10:135655-47688677)x4	ARL5B, LARP4B +180 more	Copy number gain	Mosaic supernumerary isodicentric chromosome 10	Gnot provided
Select item 815322	GRCh37/hg19 10p12.32-12.31(chr10:18600279-20348839)x3	NSUN6, CACNB2 +2 more	Copy number gain	not provided	GUncertain significance
Select item 599307	Single allele	ITIH2, ITIH5 +72 more	Deletion	Hypoparathyroidism, deafness, renal disease syndrome	GPathogenic
Select item 563780	GRCh37/hg19 10p12.31(chr10:18866867-20767945)x3	NSUN6, PLXDC2 +1 more	Copy number gain	not provided	GUncertain significance
Select item 563762	GRCh37/hg19 10p12.33-12.31(chr10:18438918-19446074)x3	CACNB2, ARL5B +1 more	Copy number gain	not provided	GUncertain significance
Select item 443260	GRCh37/hg19 10p15.3-q11.23(chr10:100026-50961640)x3	ABI1, ACBD5 +205 more	Copy number gain	See cases	GPathogenic
Select item 442109	GRCh37/hg19 10p13-12.31(chr10:15966534-19063585)x1	ARL5B, C1QL3 +11 more	Copy number loss	See cases	GUncertain significance
Select item 441987	GRCh37/hg19 10p15.3-q26.3(chr10:100027-135427143)	INA, INPP5A +721 more	Copy number gain	See cases	GPathogenic
Select item 441986	GRCh37/hg19 10p15.3-q26.3(chr10:100027-135427143)x3	A1CF, ABCC2 +721 more	Copy number gain	See cases	GPathogenic
Select item 441870	GRCh37/hg19 10p13-12.31(chr10:16624071-19846248)x3	ARL5B, CACNB2 +9 more	Copy number gain	See cases	GUncertain significance
Select item 393995	GRCh37/hg19 10p15.3-q26.3(chr10:93297-135378918)x3	A1CF, ABCC2 +722 more	Copy number gain	See cases	GPathogenic
Select item 221471	GRCh37/hg19 10p12.33-12.31(chr10:18439858-20357134)x3	ARL5B, CACNB2 +2 more	Copy number gain	Breast ductal adenocarcinoma	GUncertain significance

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Items: 26