LILRA3[gene] - ClinVar

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Items: 28

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 151481	GRCh37/hg19 19q13.42(chr19:54769799-54835745)x3	LILRA3, LILRA5 +6 more	Copy number gain	See cases	GBenign
Select item 151454	GRCh37/hg19 19q13.42(chr19:54769799-54864136)x3	LOC126862931, LAIR1 +10 more	Copy number gain	See cases	GLikely benign
Select item 2249453	NM_006865.5(LILRA3):c.962A>T (p.Gln321Leu)	LILRA3 (Q257L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2650445	NM_006865.5(LILRA3):c.933C>T (p.Ser311=)	LILRA3	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2360545	NM_006865.5(LILRA3):c.923C>T (p.Ser308Leu)	LILRA3 (S244L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2650446	NM_006865.5(LILRA3):c.894C>T (p.Ser298=)	LILRA3	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2650447	NM_006865.5(LILRA3):c.802C>T (p.Arg268Cys)	LILRA3 (R204C +1 more)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 2219599	NM_006865.5(LILRA3):c.749C>T (p.Ala250Val)	LILRA3 (A186V +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2237818	NM_006865.5(LILRA3):c.689T>G (p.Val230Gly)	LILRA3 (V166G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2206666	NM_006865.5(LILRA3):c.425C>G (p.Thr142Ser)	LILRA3 (T142S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2241971	NM_006865.5(LILRA3):c.59A>G (p.His20Arg)	LILRA3, LOC126057115 (H20R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2684892	GRCh37/hg19 19q13.33-13.43(chr19:49625130-57647352)x3	ACP4, ADM5 +261 more	Copy number gain	not provided	GLikely pathogenic
Select item 2672793	GRCh37/hg19 19q13.42(chr19:54544215-54881884)x3	CNOT3, LAIR1 +18 more	Copy number gain	not provided	GUncertain significance
Select item 1443808	NC_000019.9:g.(?_54297303)_(55678016_?)dup	TSEN34, TTYH1 +51 more	Duplication	not provided	GUncertain significance
Select item 980772	GRCh37/hg19 19q13.42-13.43(chr19:54334195-56434037)x3	TMC4, TMEM150B +87 more	Copy number gain	not provided	GUncertain significance
Select item 980771	GRCh37/hg19 19q13.42(chr19:54659105-54916280)x3	CNOT3, LAIR1 +12 more	Copy number gain	not provided	GUncertain significance
Select item 980768	GRCh37/hg19 19q13.33-13.43(chr19:48463931-57095254)x3	FLT3LG, FPR1 +308 more	Copy number gain	not provided	GPathogenic
Select item 816093	GRCh37/hg19 19q13.42(chr19:54701333-55536206)x3	CDC42EP5, FCAR +28 more	Copy number gain	not provided	GUncertain significance
Select item 816092	GRCh37/hg19 19q13.42(chr19:54474844-55181741)x3	CACNG6, CACNG8 +29 more	Copy number gain	not provided	GUncertain significance
Select item 564606	GRCh37/hg19 19q13.42-13.43(chr19:54196216-58759679)x3	ZNF548, ZNF549 +157 more	Copy number gain	not provided	GPathogenic
Select item 564602	GRCh37/hg19 19q13.42(chr19:53867570-55833460)x3	BRSK1, CACNG6 +68 more	Copy number gain	not provided	GUncertain significance
Select item 443499	GRCh37/hg19 19p13.3-q13.43(chr19:260912-58956888)	BICRA, BLOC1S3 +1364 more	Copy number gain	See cases	GPathogenic
Select item 443498	GRCh37/hg19 19p13.3-q13.43(chr19:260912-58956888)x3	A1BG, ABCA7 +1364 more	Copy number gain	See cases	GPathogenic
Select item 425531	GRCh37/hg19 19q13.42(chr19:54754462-54866330)x3	LAIR1, LILRA3 +4 more	Copy number gain	not provided	GUncertain significance
Select item 394573	GRCh37/hg19 19q13.42(chr19:54726783-54844690)x3	LILRA3, LILRA5 +4 more	Copy number gain	See cases	GBenign
Select item 394342	GRCh37/hg19 19q13.33-13.43(chr19:50489390-59095359)x3	A1BG, ACP4 +280 more	Copy number gain	See cases	GPathogenic
Select item 221404	GRCh37/hg19 19q13.42(chr19:54710237-55648526)x1	LILRB3, CDC42EP5 +32 more	Copy number loss	Breast ductal adenocarcinoma	GUncertain significance
Select item 221353	chr19:54754752-55624113 complex variant	FCAR, EPS8L1 +28 more	Complex	Breast ductal adenocarcinoma	GUncertain significance

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Items: 28