ClinVar for Gene (Select 11025) - ClinVar

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Links from Gene

Items: 85

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3341573	NM_024318.5(LILRA6):c.195C>T (p.Ser65=)	LILRA6, LILRB3	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 3290717	NM_006864.4(LILRB3):c.194G>A (p.Ser65Asn)	LILRB3 (S65N)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3290716	NM_006864.4(LILRB3):c.1112T>A (p.Met371Lys)	LILRB3 (M371K)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 3290715	NM_006864.4(LILRB3):c.1057A>G (p.Thr353Ala)	LILRB3 (T353A)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3290714	NM_006864.4(LILRB3):c.1133A>G (p.Gln378Arg)	LILRB3 (Q378R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3242700	NC_000019.9:g.(?_54621659)_(54797848_?)dup	CNOT3, LENG1 +9 more	Duplication	not provided	GUncertain significance
Select item 3118808	NM_006864.4(LILRB3):c.422C>T (p.Thr141Ile)	LILRB3 (T141I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3118807	NM_006864.4(LILRB3):c.418A>G (p.Met140Val)	LILRB3 (M140V)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 3118806	NM_006864.4(LILRB3):c.377T>G (p.Leu126Arg)	LILRB3 (L126R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3118805	NM_006864.4(LILRB3):c.202C>T (p.Pro68Ser)	LILRB3 (P68S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3118804	NM_006864.4(LILRB3):c.193A>G (p.Ser65Gly)	LILRB3 (S65G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3118803	NM_006864.4(LILRB3):c.1888A>G (p.Ile630Val)	LILRB3 (I630V +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3118802	NM_006864.4(LILRB3):c.1846G>A (p.Gly616Arg)	LILRB3 (G616R +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3118801	NM_006864.4(LILRB3):c.1572C>G (p.Asp524Glu)	LILRB3 (D524E +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 3118800	NM_006864.4(LILRB3):c.1516G>C (p.Ala506Pro)	LILRB3 (A523P +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3118799	NM_006864.4(LILRB3):c.1357G>A (p.Val453Ile)	LILRB3 (V453I +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 3118798	NM_006864.4(LILRB3):c.1192G>A (p.Gly398Ser)	LILRB3 (G398S)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 3118796	NM_006864.4(LILRB3):c.1134G>C (p.Gln378His)	LILRB3 (Q378H)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3118795	NM_006864.4(LILRB3):c.1124A>C (p.His375Pro)	LILRB3 (H375P)	Single nucleotide variant (missense variant +1 more)	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 2650429	NM_006864.4(LILRB3):c.1095A>G (p.Pro365=)	LILRB3, LILRA6	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2650428	NM_006864.4(LILRB3):c.1096C>T (p.Leu366=)	LILRA6, LILRB3	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2615878	NM_006864.4(LILRB3):c.1745C>G (p.Thr582Ser)	LILRB3 (T582S +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2609086	NM_006864.4(LILRB3):c.1181A>T (p.Tyr394Phe)	LILRB3 (Y394F)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2605378	NM_006864.4(LILRB3):c.527G>T (p.Gly176Val)	LILRB3 (G176V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2546492	NM_006864.4(LILRB3):c.884G>C (p.Arg295Thr)	LILRB3 (R295T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2536694	NM_006864.4(LILRB3):c.188A>G (p.Glu63Gly)	LILRB3 (E63G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2533097	NM_006864.4(LILRB3):c.547G>A (p.Val183Met)	LILRB3 (V183M)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2527683	NM_006864.4(LILRB3):c.643G>C (p.Glu215Gln)	LILRB3 (E215Q)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2521304	NM_006864.4(LILRB3):c.1020C>A (p.Asn340Lys)	LILRB3 (N340K)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2519162	NM_006864.4(LILRB3):c.1394T>A (p.Leu465His)	LILRB3 (L482H +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2513463	NM_006864.4(LILRB3):c.343C>G (p.Leu115Val)	LILRB3 (L115V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2510098	NM_006864.4(LILRB3):c.1814G>C (p.Arg605Pro)	LILRB3 (R605P +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2460161	NM_006864.4(LILRB3):c.1042= (p.Arg348=)	LILRB3	Variation (no sequence alteration +1 more)	not specified	GUncertain significance
Select item 2455680	NM_006864.4(LILRB3):c.290G>A (p.Arg97His)	LILRB3 (R97H)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2406962	NM_006864.4(LILRB3):c.1207A>G (p.Asn403Asp)	LILRB3 (N403D)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2406961	NM_006864.4(LILRB3):c.1202G>A (p.Ser401Asn)	LILRB3 (S401N)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2385386	NM_006864.4(LILRB3):c.988C>G (p.Gln330Glu)	LILRB3 (Q330E)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2378715	NM_006864.4(LILRB3):c.417T>A (p.Asn139Lys)	LILRB3 (N139K)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2377147	NM_006864.4(LILRB3):c.333C>A (p.Asp111Glu)	LILRB3 (D111E)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2363634	NM_006864.4(LILRB3):c.1450C>T (p.Arg484Cys)	LILRB3 (R484C +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2354898	NM_006864.4(LILRB3):c.1744A>G (p.Thr582Ala)	LILRB3 (T583A +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2354300	NM_006864.4(LILRB3):c.1222T>A (p.Ser408Thr)	LILRB3 (S408T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2351755	NM_006864.4(LILRB3):c.1208A>T (p.Asn403Ile)	LILRB3 (N403I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2351754	NM_006864.4(LILRB3):c.1207A>T (p.Asn403Tyr)	LILRB3 (N403Y)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2351753	NM_006864.4(LILRB3):c.1205C>T (p.Ser402Phe)	LILRB3 (S402F)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2351752	NM_006864.4(LILRB3):c.1203C>A (p.Ser401Arg)	LILRB3 (S401R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2347456	NM_006864.4(LILRB3):c.1346C>T (p.Ser449Leu)	LILRB3 (S449L +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2319182	NM_006864.4(LILRB3):c.4A>C (p.Thr2Pro)	LILRB3 (T2P)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2312061	NM_006864.4(LILRB3):c.1436A>C (p.Lys479Thr)	LILRB3 (K479T +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2301849	NM_006864.4(LILRB3):c.334C>G (p.Pro112Ala)	LILRB3 (P112A)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2288077	NM_006864.4(LILRB3):c.527G>C (p.Gly176Ala)	LILRB3 (G176A)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2284071	NM_006864.4(LILRB3):c.1522G>A (p.Val508Ile)	LILRB3 (V525I +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2260675	NM_006864.4(LILRB3):c.644A>G (p.Glu215Gly)	LILRB3 (E215G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2250097	NM_006864.4(LILRB3):c.400G>T (p.Val134Leu)	LILRB3 (V134L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2235477	NM_006864.4(LILRB3):c.1060T>G (p.Phe354Val)	LILRB3 (F354V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2211188	NM_006864.4(LILRB3):c.1592A>G (p.Gln531Arg)	LILRB3 (Q531R +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2211187	NM_006864.4(LILRB3):c.1589G>C (p.Ser530Thr)	LILRB3 (S547T +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2211186	NM_006864.4(LILRB3):c.1582C>A (p.Leu528Met)	LILRB3 (L528M +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 1443808	NC_000019.9:g.(?_54297303)_(55678016_?)dup	CACNG6, CACNG7 +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	PPP1R15A, PPP2R1A +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)	PGLYRP1, PGLYRP2 +1364 more	Copy number gain	See cases	GPathogenic
Select item 443498	GRCh37/hg19 19p13.3-q13.43(chr19:260912-58956888)x3	TMC4, TMED1 +1364 more	Copy number gain	See cases	GPathogenic
Select item 395635	GRCh37/hg19 19q13.42(chr19:54726783-54746032)x1	LILRA6, LILRB3	Copy number loss	See cases	GBenign
Select item 395634	GRCh37/hg19 19q13.42(chr19:54726783-54746032)x3	LILRA6, LILRB3	Copy number gain	See cases	GBenign
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 394329	GRCh37/hg19 19q13.42(chr19:54726783-54744331)x1	LILRA6, LILRB3	Copy number loss	See cases	GBenign
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 153721	GRCh38/hg38 19q13.41-13.43(chr19:52143873-58445521)x3	A1BG, A1BG-AS1 +547 more	Copy number gain	See cases	GPathogenic
Select item 146579	GRCh38/hg38 19q13.33-13.43(chr19:50152520-58581203)x3	OSCAR, PEG3 +782 more	Copy number gain	See cases	GPathogenic
Select item 144762	GRCh38/hg38 19q13.41-13.43(chr19:52612432-58581203)x3	SSC5D, SYT5 +553 more	Copy number gain	See cases	GPathogenic
Select item 144709	GRCh38/hg38 19q13.41-13.43(chr19:52955056-58581203)x3	TMC4, TMEM150B +537 more	Copy number gain	See cases	GPathogenic
Select item 59127	GRCh38/hg38 19q13.41-13.43(chr19:51141518-58539965)x3	A1BG, A1BG-AS1 +647 more	Copy number gain	See cases	GPathogenic
Select item 59126	GRCh38/hg38 19q13.33-13.43(chr19:49907832-58557889)x3	LOC130065082, LOC130065083 +806 more	Copy number gain	See cases	GPathogenic
Select item 59117	GRCh38/hg38 19q13.33-13.43(chr19:47929575-58572206)x3	LOC130064903, LOC130064904 +1093 more	Copy number gain	See cases	GPathogenic
Select item 59116	GRCh38/hg38 19q13.33-13.43(chr19:47908540-58539965)x3	LOC130064925, LOC130064926 +1081 more	Copy number gain	See cases	GPathogenic
Select item 57219	GRCh38/hg38 19q13.33-13.43(chr19:50191219-58535818)x3	LOC130065034, LOC130065035 +761 more	Copy number gain	See cases	GPathogenic

ClinVar

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Links from Gene

Items: 85