ClinVar for Gene (Select 4110) - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3366901	NC_000023.10:g.(?_54610638)_(154689386_?)dup	ABCB7, ABCD1 +526 more	Duplication	Hereditary factor VIII deficiency disease	GUncertain significance
Select item 3292583	NM_005366.5(MAGEA11):c.396C>G (p.Asp132Glu)	MAGEA11 (D103E +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3242589	GRCh38/hg38 Xp22.33-q28(chrX:2757837-156030895)x2	LOC130068417, LOC130068418 +2599 more	Copy number gain	Klinefelter syndrome	GPathogenic
Select item 3148884	GRCh37/hg19 Xq25-28(chrX:125253445-155233098)x1	PRR32, ABCD1 +215 more	Copy number loss	See cases	GPathogenic
Select item 3148864	GRCh37/hg19 Xq25-28(chrX:121656905-155233098)x1	SLITRK2, SLITRK4 +221 more	Copy number loss	not provided	GPathogenic
Select item 3122061	NM_005366.5(MAGEA11):c.915T>A (p.Asn305Lys)	MAGEA11 (N276K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3122060	NM_005366.5(MAGEA11):c.421C>T (p.Leu141Phe)	MAGEA11 (L112F +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3122059	NM_005366.5(MAGEA11):c.238A>G (p.Thr80Ala)	MAGEA11 (T51A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3062552	GRCh37/hg19 Xq27.3-28(chrX:144487227-148811395)	AFF2, CXorf51A +16 more	Copy number gain	not specified	GLikely pathogenic
Select item 3062491	GRCh37/hg19 Xq24-28(chrX:119395676-154930047)	TAFAZZIN, TENM1 +241 more	Copy number loss	not specified	GPathogenic
Select item 3062473	GRCh37/hg19 Xq22.2-28(chrX:103405294-155233731)	ABCD1, ACSL4 +321 more	Copy number loss	not specified	GPathogenic
Select item 3049970	NM_005366.5(MAGEA11):c.267-5C>T	MAGEA11	Single nucleotide variant (intron variant)	MAGEA11-related disorder	GLikely benign
Select item 3044833	NM_005366.5(MAGEA11):c.573C>A (p.Ser191Arg)	MAGEA11 (S162R +1 more)	Single nucleotide variant (missense variant)	MAGEA11-related disorder	GLikely benign
Select item 3034896	NM_005366.5(MAGEA11):c.900T>C (p.Asp300=)	MAGEA11	Single nucleotide variant (synonymous variant)	MAGEA11-related disorder	GLikely benign
Select item 3024654	GRCh37/hg19 Xq12-28(chrX:67292994-155240074)x3	CT47A5, NXF3 +488 more	Copy number gain	not provided	GPathogenic
Select item 2685724	GRCh37/hg19 Xq28(chrX:148598351-154943978)x1	ABCD1, ARHGAP4 +110 more	Copy number loss	not provided	GPathogenic
Select item 2685718	GRCh37/hg19 Xq24-28(chrX:119071609-155233731)x1	ABCD1, ACTRT1 +246 more	Copy number loss	not provided	GPathogenic
Select item 2685717	GRCh37/hg19 Xq24-28(chrX:118576752-155233731)x1	ABCD1, ACTRT1 +258 more	Copy number loss	not provided	GPathogenic
Select item 2685023	GRCh37/hg19 Xq28(chrX:148782000-149715472)x3	EOLA2, HSFX1 +4 more	Copy number gain	not provided	GUncertain significance
Select item 2685022	GRCh37/hg19 Xq28(chrX:148570605-148827774)x3	MAGEA9B, EOLA1 +4 more	Copy number gain	not provided	GUncertain significance
Select item 2665033	GRCh38/hg38 Xq27.3-28(chrX:143293592-149749234)	AFF2, CXorf51A +74 more	Copy number gain	Mucopolysaccharidosis, MPS-II	GUncertain significance
Select item 2661621	NM_005366.5(MAGEA11):c.854C>G (p.Thr285Ser)	MAGEA11 (T256S +1 more)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 2661620	NM_005366.5(MAGEA11):c.456C>T (p.Ser152=)	MAGEA11	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2617048	NM_005366.5(MAGEA11):c.988C>T (p.Pro330Ser)	MAGEA11 (P330S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2556543	NM_005366.5(MAGEA11):c.301G>A (p.Val101Ile)	MAGEA11 (V101I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2527616	NM_005366.5(MAGEA11):c.790T>C (p.Phe264Leu)	MAGEA11 (F235L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2506546	GRCh37/hg19 Xp22.33-q28(chrX:200855-155240074)	ABCB7, ABCD1 +818 more	Copy number gain	Klinefelter syndrome	GPathogenic
Select item 2501299	GRCh37/hg19 Xq28(chrX:148564272-148836483)	EOLA1, HSFX1 +5 more	Copy number gain	See cases	GLikely benign
Select item 2497748	GRCh37/hg19 Xq27.1-28(chrX:139586015-154774957)	ABCD1, AFF2 +140 more	Copy number gain	Syndromic X-linked intellectual disability Lubs type	GPathogenic
Select item 2469879	NM_005366.5(MAGEA11):c.412G>T (p.Ala138Ser)	MAGEA11 (A109S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2445220	Single allele	EOLA1, HSFX2 +4 more	Duplication	See cases	GLikely benign
Select item 2395820	NM_005366.5(MAGEA11):c.581A>G (p.Asp194Gly)	MAGEA11 (D165G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2376120	NM_005366.5(MAGEA11):c.17G>A (p.Arg6His)	MAGEA11 (R6H)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2361245	NM_005366.5(MAGEA11):c.247A>G (p.Ile83Val)	MAGEA11 (I54V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2259044	NM_005366.5(MAGEA11):c.305G>A (p.Arg102Gln)	MAGEA11 (R73Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2241080	NM_005366.5(MAGEA11):c.80G>A (p.Gly27Glu)	MAGEA11 (G27E)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2222525	NM_005366.5(MAGEA11):c.1217C>T (p.Ala406Val)	MAGEA11 (A377V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1808722	GRCh37/hg19 Xq25-28(chrX:124749464-155233731)x1	ABCD1, ACTRT1 +216 more	Copy number loss	not provided	GPathogenic
Select item 1808671	GRCh37/hg19 Xq27.1-28(chrX:139493806-148855992)x1	AFF2, CDR1 +34 more	Copy number loss	not provided	GPathogenic
Select item 1807692	GRCh37/hg19 Xq27.1-28(chrX:139504564-149382013)x2	AFF2, CDR1 +37 more	Copy number gain	not provided	GPathogenic
Select item 1710916	GRCh37/hg19 Xq27.3-28(chrX:142401540-155233731)x1	ABCD1, BCAP31 +129 more	Copy number loss	See cases	GPathogenic
Select item 1707442	GRCh37/hg19 Xp22.2-q28(chrX:11522765-155233731)x1	ABCB7, ABCD1 +790 more	Copy number loss	See cases	GPathogenic
Select item 1706520	GRCh37/hg19 Xq21.1-28(chrX:77670699-155233731)x1	NXF5, NXT2 +414 more	Copy number loss	See cases	GPathogenic
Select item 1704345	GRCh37/hg19 Xp22.33-q28(chrX:61545-155226048)x2	ABCB7, ABCD1 +818 more	Copy number gain	Klinefelter syndrome	GPathogenic
Select item 1703584	GRCh37/hg19 Xq11.1-28(chrX:62685885-155233731)	ABCB7, ABCD1 +501 more	Copy number loss	Turner syndrome	GPathogenic
Select item 1703580	GRCh37/hg19 Xp22.33-q28(chrX:1-155270560)	ABCB7, ABCD1 +819 more	Copy number loss	Turner syndrome	GPathogenic
Select item 1703579	GRCh37/hg19 Xp22.33-q28(chrX:1-155270560)	AKAP14, CT47A11 +819 more	Copy number gain	Hypotonia +2 more	GPathogenic
Select item 1526863	GRCh37/hg19 Xq27.3-28(chrX:146752853-150192253)	AFF2, CD99L2 +17 more	Copy number loss	not specified	GPathogenic
Select item 1342311	Single allele	ABCD1, AFF2 +337 more	Duplication	Syndromic X-linked intellectual disability Lubs type	GPathogenic
Select item 1341233	GRCh37/hg19 Xp22.33-q28(chrX:168546-155233731)x1	RADX, RAI2 +818 more	Copy number loss	not provided	GPathogenic
Select item 1341223	GRCh37/hg19 Xp22.33-q28(chrX:168546-155233731)x3	GPM6B, KLHL15 +818 more	Copy number gain	not provided	GPathogenic
Select item 1180551	GRCh37/hg19 Xp22.33-q28(chrX:60000-155234966)x1	KLHL34, KLHL4 +818 more	Copy number loss	not provided	GPathogenic
Select item 1180513	GRCh37/hg19 Xq27.1-28(chrX:139484271-149442579)x1	AFF2, CDR1 +37 more	Copy number loss	not provided	GPathogenic
Select item 1077156	GRCh38/hg38 Xq27.3-28(chrX:145728205-150464413)x1	LOC130068788, LOC130068789 +104 more	Copy number loss	Mucopolysaccharidosis, MPS-II	GPathogenic
Select item 992648	GRCh37/hg19 Xp11.21-q28(chrX:56469080-155233731)x3	CPXCR1, GABRE +509 more	Copy number gain	not provided	GPathogenic
Select item 983156	GRCh37/hg19 Xp11.21-q28(chrX:55507789-155198481)x3	ARMCX4, CXorf51B +513 more	Copy number gain	See cases	GPathogenic
Select item 980880	GRCh37/hg19 Xq28(chrX:148448248-148855992)x4	EOLA1, HSFX1 +5 more	Copy number gain	not provided	GLikely benign
Select item 980879	GRCh37/hg19 Xq28(chrX:148538098-148855992)x3	HSFX2, EOLA1 +5 more	Copy number gain	not provided	GLikely benign
Select item 979836	GRCh37/hg19 Xq21.33-28(chrX:94264404-155233731)x1	ABCD1, ACSL4 +387 more	Copy number loss	not provided	GPathogenic
Select item 916135	GRCh37/hg19 Xq25-28(chrX:122132166-155097214)	APLN, ABCD1 +221 more	Copy number loss	Intellectual disability	GLikely pathogenic
Select item 816405	GRCh37/hg19 Xq28(chrX:148392776-148855992)x4	TMEM185A, HSFX2 +5 more	Copy number gain	not provided	GLikely benign
Select item 816403	GRCh37/hg19 Xq28(chrX:148267375-148827859)x3	TMEM185A, HSFX2 +4 more	Copy number gain	not provided	GLikely benign
Select item 816368	GRCh37/hg19 Xq21.1-28(chrX:84387417-155233731)x1	ABCD1, ACSL4 +398 more	Copy number loss	not provided	GPathogenic
Select item 816364	GRCh37/hg19 Xq21.1-28(chrX:78444738-155233731)x1	ABCD1, ACSL4 +410 more	Copy number loss	not provided	GPathogenic
Select item 688542	GRCh37/hg19 Xq28(chrX:148266957-148830292)x3	EOLA1, HSFX2 +4 more	Copy number gain	not provided	GUncertain significance
Select item 688406	GRCh37/hg19 Xq25-28(chrX:122924044-155233731)x1	ABCD1, ACTRT1 +220 more	Copy number loss	not provided	GPathogenic
Select item 688137	GRCh37/hg19 Xp22.33-q28(chrX:168546-155233731)x1	ARHGAP36, ARHGAP4 +818 more	Copy number loss	not provided	GPathogenic
Select item 687891	GRCh37/hg19 Xq28(chrX:148570603-148832908)x3	EOLA1, HSFX2 +4 more	Copy number gain	not provided	GUncertain significance
Select item 687519	GRCh37/hg19 Xp11.21-q28(chrX:54941868-155233731)x1	AWAT1, AWAT2 +524 more	Copy number loss	not provided	GUncertain significance
Select item 687132	GRCh37/hg19 Xq24-28(chrX:118150047-155233731)x1	ABCD1, ACTRT1 +262 more	Copy number loss	not provided	GPathogenic
Select item 686822	GRCh37/hg19 Xq28(chrX:148266957-148884123)x2	EOLA1, HSFX1 +6 more	Copy number gain	not provided	GUncertain significance
Select item 686250	GRCh37/hg19 Xq22.3-28(chrX:104098124-155233731)x1	ABCD1, ACSL4 +320 more	Copy number loss	not provided	GPathogenic
Select item 685906	GRCh37/hg19 Xq28(chrX:148570607-148827859)x2	EOLA1, HSFX2 +4 more	Copy number gain	not provided	GUncertain significance
Select item 685716	GRCh37/hg19 Xq27.1-28(chrX:139513270-149234353)x2	AFF2, CDR1 +37 more	Copy number gain	not provided	GPathogenic
Select item 685566	GRCh37/hg19 Xp11.1-q28(chrX:58455352-155233731)x1	AWAT2, BCAP31 +502 more	Copy number loss	not provided	GPathogenic
Select item 685331	GRCh37/hg19 Xp22.33-q28(chrX:168546-155233731)x4	BEX1, BEX2 +818 more	Copy number gain	not provided	GPathogenic
Select item 684964	GRCh37/hg19 Xq21.32-28(chrX:92814516-155233731)x1	AIFM1, CXorf51A +389 more	Copy number loss	not provided	GPathogenic
Select item 626291	Single allele	AKAP14, CCDC22 +733 more	Duplication	Syndromic X-linked intellectual disability Lubs type	GPathogenic
Select item 625854	GRCh37/hg19 Xq25-28(chrX:122757437-155208244)x1	ABCD1, ACTRT1 +221 more	Copy number loss	Premature ovarian insufficiency	GLikely pathogenic
Select item 625671	GRCh37/hg19 Xq26.3-28(chrX:134975270-155233945)	ABCD1, ADGRG4 +160 more	Copy number gain	not provided	GPathogenic
Select item 564923	GRCh37/hg19 Xq28(chrX:148639911-149404134)x2	MAGEA11, MAGEA9B +6 more	Copy number gain	not provided	GUncertain significance
Select item 564922	GRCh37/hg19 Xq28(chrX:148581602-148827774)x2	MAGEA11, EOLA1 +4 more	Copy number gain	not provided	GLikely benign
Select item 564921	GRCh37/hg19 Xq28(chrX:148566841-148875584)x3	TMEM185A, MAGEA9 +6 more	Copy number gain	not provided	GLikely benign
Select item 564919	GRCh37/hg19 Xq28(chrX:147680249-149682911)x2	MAGEA9, MAGEA11 +10 more	Copy number gain	not provided	GUncertain significance
Select item 564913	GRCh37/hg19 Xq27.2-28(chrX:140388077-155233731)x3	ABCD1, AFF2 +136 more	Copy number gain	not provided	GPathogenic
Select item 564912	GRCh37/hg19 Xq27.1-28(chrX:139504488-155233731)x1	ABCD1, AFF2 +141 more	Copy number loss	not provided	GPathogenic
Select item 564908	GRCh37/hg19 Xq27.1-28(chrX:138331745-155233731)x1	ABCD1, AFF2 +145 more	Copy number loss	not provided	GPathogenic
Select item 564897	GRCh37/hg19 Xq25-28(chrX:125733292-155233846)x1	ABCD1, ACTRT1 +214 more	Copy number loss	not provided	GPathogenic
Select item 564884	GRCh37/hg19 Xq22.3-28(chrX:107823442-155233731)x1	FMR1-AS1, FMR1NB +297 more	Copy number loss	not provided	GPathogenic
Select item 564874	GRCh37/hg19 Xq22.1-28(chrX:99324651-155233731)x1	ABCD1, ACSL4 +385 more	Copy number loss	not provided	GPathogenic
Select item 564868	GRCh37/hg19 Xq21.31-28(chrX:91140025-155233731)x1	ABCD1, ACSL4 +390 more	Copy number loss	not provided	GPathogenic
Select item 560083	Single allele	HSFX1, MAGEA9 +4 more	Duplication	not provided	GUncertain significance
Select item 488014	Single allele	ARSF, CFAP47 +2632 more	Duplication	Autism +1 more	GPathogenic
Select item 443974	GRCh37/hg19 Xp22.33-q28(chrX:168547-155233731)	ABCB7, ABCD1 +818 more	Copy number gain	See cases	GPathogenic
Select item 443724	GRCh37/hg19 Xq27.3-28(chrX:146232592-155233731)x1	ABCD1, AFF2 +120 more	Copy number loss	See cases	GPathogenic
Select item 443630	GRCh37/hg19 Xq23-28(chrX:112474054-155233731)x1	LRCH2, LUZP4 +277 more	Copy number loss	See cases	GPathogenic
Select item 443504	GRCh37/hg19 Xp21.2-q28(chrX:31088082-155233731)x1	PNMA5, PNMA6A +695 more	Copy number loss	See cases	GPathogenic
Select item 443017	GRCh37/hg19 Xp11.21-q28(chrX:56457791-155233731)x3	NAA10, NALF2 +509 more	Copy number gain	See cases	GPathogenic
Select item 442965	GRCh37/hg19 Xq26.3-28(chrX:133944147-155233731)x3	VGLL1, VMA21 +174 more	Copy number gain	See cases	GPathogenic
Select item 442945	GRCh37/hg19 Xq21.1-28(chrX:78230501-155233731)x1	ABCD1, ACSL4 +410 more	Copy number loss	See cases	GPathogenic

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