ClinVar for Gene (Select 10495) - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3275464	NM_006375.4(ENOX2):c.1441T>C (p.Cys481Arg)	ENOX2 (C510R +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3275463	NM_006375.4(ENOX2):c.386G>A (p.Arg129His)	ENOX2 (R129H +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3275462	NM_006375.4(ENOX2):c.621G>C (p.Leu207Phe)	ENOX2 (L207F +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3275461	NM_006375.4(ENOX2):c.1231G>A (p.Gly411Ser)	ENOX2 (G409S +4 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 3088940	NM_006375.4(ENOX2):c.569G>A (p.Arg190His)	ENOX2 (R190H +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3088939	NM_006375.4(ENOX2):c.416G>A (p.Arg139His)	ENOX2 (R139H +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3088938	NM_006375.4(ENOX2):c.313G>A (p.Gly105Ser)	ENOX2 (G105S +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3088937	NM_006375.4(ENOX2):c.148A>G (p.Met50Val)	ENOX2 (M142V +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3088936	NM_006375.4(ENOX2):c.-38-6023T>G	ENOX2 (F5L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
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 3024654	GRCh37/hg19 Xq12-28(chrX:67292994-155240074)x3	CPXCR1, MAGEE2 +488 more	Copy number gain	not provided	GPathogenic
Select item 2685767	GRCh37/hg19 Xq26.1(chrX:129639553-129849174)x2	ENOX2	Copy number gain	not provided	GUncertain significance
Select item 2685720	GRCh37/hg19 Xq26.1-26.3(chrX:129627661-135812056)x1	ADGRG4, ARHGAP36 +46 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 2617985	NM_006375.4(ENOX2):c.886C>G (p.Leu296Val)	ENOX2 (L325V +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2558886	NM_006375.4(ENOX2):c.1474G>C (p.Glu492Gln)	ENOX2 (E521Q +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2555008	NM_006375.4(ENOX2):c.640C>G (p.Pro214Ala)	ENOX2 (P214A +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2554057	NM_006375.4(ENOX2):c.1037A>T (p.Asp346Val)	ENOX2 (D375V +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2507658	NM_006375.4(ENOX2):c.1465T>C (p.Tyr489His)	ENOX2 (Y489H +4 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 2495655	NM_006375.4(ENOX2):c.232A>G (p.Thr78Ala)	ENOX2 (T107A +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2410093	NM_006375.4(ENOX2):c.169G>A (p.Val57Ile)	ENOX2 (V57I +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2407017	NM_006375.4(ENOX2):c.818G>A (p.Arg273His)	ENOX2 (R365H +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2376952	NM_006375.4(ENOX2):c.71G>C (p.Gly24Ala)	ENOX2 (G53A +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2375693	NM_006375.4(ENOX2):c.623G>A (p.Arg208His)	ENOX2 (R208H +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2375643	NM_006375.4(ENOX2):c.530A>G (p.Gln177Arg)	ENOX2 (Q206R +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2323977	NM_006375.4(ENOX2):c.1520T>G (p.Leu507Arg)	ENOX2 (L534R +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2308238	NM_006375.4(ENOX2):c.1739T>C (p.Leu580Pro)	ENOX2 (L578P +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2298900	NM_006375.4(ENOX2):c.743A>G (p.Glu248Gly)	ENOX2 (E340G +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2212183	NM_006375.4(ENOX2):c.1433C>G (p.Ser478Cys)	ENOX2 (S476C +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1809416	GRCh37/hg19 Xq26.1(chrX:129639553-129858717)x3	ENOX2	Copy number gain	not provided	GUncertain significance
Select item 1809363	GRCh37/hg19 Xq26.1(chrX:129667394-130172589)x2	ENOX2	Copy number gain	not provided	GUncertain significance
Select item 1809290	GRCh37/hg19 Xq26.1(chrX:129533578-130299562)x2	ARHGAP36, ENOX2 +1 more	Copy number gain	not provided	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 1808242	GRCh37/hg19 Xq26.1(chrX:129711353-129979961)x2	ENOX2	Copy number gain	not provided	GUncertain significance
Select item 1807915	GRCh37/hg19 Xq26.1(chrX:129542798-130004339)x2	ENOX2, RBMX2	Copy number gain	not provided	GUncertain significance
Select item 1710922	GRCh37/hg19 Xq26.1-26.2(chrX:129711889-132794615)x3	ARHGAP36, ENOX2 +11 more	Copy number gain	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 1526848	GRCh37/hg19 Xq25-26.2(chrX:126307810-131646710)	ACTRT1, AIFM1 +22 more	Copy number gain	not specified	GPathogenic
Select item 1341304	GRCh37/hg19 Xq26.1(chrX:129666782-130172589)x3	ENOX2	Copy number gain	not provided	GUncertain significance
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 1339995	GRCh37/hg19 Xq26.1(chrX:129769240-130230464)x2	ARHGAP36, ENOX2	Copy number gain	not provided	GUncertain significance
Select item 1180551	GRCh37/hg19 Xp22.33-q28(chrX:60000-155234966)x1	KLHL34, KLHL4 +818 more	Copy number loss	not provided	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 980319	GRCh37/hg19 Xq24-26.1(chrX:117120780-129850994)x3	C1GALT1C1, CT47A1 +69 more	Copy number gain	not provided	GPathogenic
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 816392	GRCh37/hg19 Xq26.1(chrX:129769236-130228660)x2	ENOX2, ARHGAP36	Copy number gain	not provided	GUncertain significance
Select item 816382	GRCh37/hg19 Xq24-26.1(chrX:117119895-129850963)x2	ACTRT1, AIFM1 +69 more	Copy number gain	not provided	GPathogenic
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 789254	NM_006375.4(ENOX2):c.1129+6G>A	ENOX2	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 764769	NM_006375.4(ENOX2):c.1188C>T (p.Leu396=)	ENOX2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 719414	NM_006375.4(ENOX2):c.1470T>C (p.Pro490=)	ENOX2	Single nucleotide variant (synonymous variant)	not provided	GBenign
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 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 686250	GRCh37/hg19 Xq22.3-28(chrX:104098124-155233731)x1	ABCD1, ACSL4 +320 more	Copy number loss	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 564901	GRCh37/hg19 Xq26.1(chrX:129770027-130160458)x3	ENOX2	Copy number gain	not provided	GUncertain significance
Select item 564898	GRCh37/hg19 Xq25-26.3(chrX:126759247-135790885)x1	ACTRT1, CT45A3 +62 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 564891	GRCh37/hg19 Xq24-27.1(chrX:120777368-139345946)x1	CT45A3, UTP14A +79 more	Copy number loss	not provided	GPathogenic
Select item 564888	GRCh37/hg19 Xq24-27.1(chrX:117998704-140159954)x3	ACTRT1, ADGRG4 +122 more	Copy number gain	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 545551	NC_000023.10:g.36649710_136649711del100000002insG	AMER1, AMMECR1 +541 more	Indel	Heterotaxy, visceral, 1, X-linked	GPathogenic
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 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 442945	GRCh37/hg19 Xq21.1-28(chrX:78230501-155233731)x1	ABCD1, ACSL4 +410 more	Copy number loss	See cases	GPathogenic
Select item 442821	GRCh37/hg19 Xq21.33-28(chrX:96499476-151870013)x3	ACSL4, ACTRT1 +303 more	Copy number gain	See cases	GUncertain significance
Select item 442724	GRCh37/hg19 Xp22.33-q28(chrX:168547-151304063)x1	AP1S2, APEX2 +731 more	Copy number loss	See cases	GPathogenic
Select item 442712	GRCh37/hg19 Xq22.1-28(chrX:98495811-155233731)x1	ABCD1, ACSL4 +384 more	Copy number loss	See cases	GPathogenic
Select item 442646	GRCh37/hg19 Xp11.21-q28(chrX:57415659-155233731)x3	OR13H1, OTUD6A +505 more	Copy number gain	See cases	GPathogenic
Select item 442531	GRCh37/hg19 Xp11.21-q28(chrX:55000501-155230750)x3	ABCB7, ABCD1 +523 more	Copy number gain	See cases	GPathogenic
Select item 442422	GRCh37/hg19 Xq21.31-28(chrX:86900388-155233731)x1	ATP11C, ATP1B4 +393 more	Copy number loss	See cases	GPathogenic
Select item 442321	GRCh37/hg19 Xp11.21-q28(chrX:57511767-155233731)x3	YIPF6, ZBTB33 +505 more	Copy number gain	See cases	GPathogenic
Select item 442262	GRCh37/hg19 Xq24-28(chrX:116621104-155233731)x1	ABCD1, ACTRT1 +266 more	Copy number loss	See cases	GPathogenic
Select item 442001	GRCh37/hg19 Xq21.1-28(chrX:79862302-155233731)x1	ABCD1, ACSL4 +406 more	Copy number loss	See cases	GPathogenic

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