ClinVar for Gene (Select 3167) - ClinVar

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Links from Gene

Items: 78

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3284528	NM_005519.2(HMX2):c.433G>A (p.Ala145Thr)	HMX2 (A145T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3284527	NM_005519.2(HMX2):c.509T>G (p.Met170Arg)	HMX2 (M170R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3148924	GRCh37/hg19 10q26.12-26.3(chr10:122331280-135426386)x1	ABRAXAS2, ACADSB +80 more	Copy number loss	not provided	GPathogenic
Select item 3106353	NM_005519.2(HMX2):c.797A>G (p.Asn266Ser)	HMX2, LOC124416925 (N266S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3106352	NM_005519.2(HMX2):c.658G>C (p.Ala220Pro)	HMX2, LOC124416925 (A220P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3106351	NM_005519.2(HMX2):c.455C>T (p.Thr152Met)	HMX2 (T152M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3106350	NM_005519.2(HMX2):c.439G>T (p.Ala147Ser)	HMX2 (A147S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3106349	NM_005519.2(HMX2):c.349A>G (p.Lys117Glu)	HMX2 (K117E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3106348	NM_005519.2(HMX2):c.275C>G (p.Pro92Arg)	HMX2 (P92R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3106347	NM_005519.2(HMX2):c.233C>T (p.Pro78Leu)	HMX2 (P78L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3063164	GRCh37/hg19 10q23.33-26.3(chr10:95078198-135427143)x3	ABCC2, ABLIM1 +293 more	Copy number gain	not specified	GPathogenic
Select item 3050215	NM_005519.2(HMX2):c.342G>A (p.Ser114=)	HMX2	Single nucleotide variant (synonymous variant)	HMX2-related disorder	GLikely benign
Select item 2684621	GRCh37/hg19 10q25.1-26.3(chr10:111447991-133435388)x3	ABLIM1, ABRAXAS2 +117 more	Copy number gain	not provided	GPathogenic
Select item 2671974	GRCh37/hg19 10q25.1-26.3(chr10:111378692-135427143)x3	ABLIM1, ABRAXAS2 +145 more	Copy number gain	Distal trisomy 10q	GPathogenic
Select item 2608826	NM_005519.2(HMX2):c.731G>A (p.Arg244His)	HMX2, LOC124416925 (R244H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2580338	GRCh37/hg19 10q26.13-26.3(chr10:124895517-135440296)x1	ABRAXAS2, ADAM12 +62 more	Copy number loss	Distal 10q deletion syndrome	GPathogenic
Select item 2574696	GRCh37/hg19 10p14-q26.3(chr10:11138692-135427143)	AGAP5, CRTAC1 +682 more	Copy number gain	Distal trisomy 10q	GPathogenic
Select item 2574693	GRCh37/hg19 10q26.13-26.3(chr10:123477898-135427143)	GLRX3, GPR26 +77 more	Copy number loss	Distal 10q deletion syndrome	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 2524687	NM_005519.2(HMX2):c.571A>G (p.Thr191Ala)	HMX2 (T191A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2517384	NM_005519.2(HMX2):c.648C>G (p.Asn216Lys)	HMX2 (N216K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2513338	NM_005519.2(HMX2):c.551C>G (p.Ser184Cys)	HMX2 (S184C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2498475	GRCh37/hg19 10q26.12-26.3(chr10:122610933-135439810)x1	ABRAXAS2, ACADSB +80 more	Copy number loss	not provided	GPathogenic
Select item 2489638	NM_005519.2(HMX2):c.601C>T (p.Arg201Cys)	HMX2 (R201C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2488671	NM_005519.2(HMX2):c.151T>A (p.Ser51Thr)	HMX2 (S51T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2471063	NM_005519.2(HMX2):c.612G>C (p.Trp204Cys)	HMX2 (W204C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2268168	NM_005519.2(HMX2):c.287G>T (p.Gly96Val)	HMX2 (G96V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2243291	NM_005519.2(HMX2):c.644C>T (p.Ala215Val)	HMX2 (A215V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2242593	NM_005519.2(HMX2):c.803A>G (p.Tyr268Cys)	HMX2, LOC124416925 (Y268C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2231022	NM_005519.2(HMX2):c.488A>G (p.Gln163Arg)	HMX2 (Q163R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2222906	NM_005519.2(HMX2):c.746C>T (p.Pro249Leu)	HMX2, LOC124416925 (P249L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1807931	GRCh37/hg19 10q26.13(chr10:124252660-125447562)x1	ACADSB, BUB3 +12 more	Copy number loss	not provided	GUncertain significance
Select item 1527609	GRCh37/hg19 10q26.12-26.3(chr10:122343861-135427143)	FAM24A, FAM24B +80 more	Copy number loss	not specified	GPathogenic
Select item 1527608	GRCh37/hg19 10q26.12-26.3(chr10:122125760-135062972)	ABRAXAS2, ACADSB +68 more	Copy number gain	not specified	GLikely pathogenic
Select item 1527606	GRCh37/hg19 10q25.3-26.13(chr10:117019650-125217066)	ACADSB, ARMS2 +54 more	Copy number loss	not specified	GPathogenic
Select item 1527605	GRCh37/hg19 10q25.1-26.3(chr10:108455687-135427143)	ABLIM1, ABRAXAS2 +146 more	Copy number gain	not specified	GPathogenic
Select item 1180521	GRCh37/hg19 10q25.3-26.3(chr10:118247181-135435319)x3	ECHS1, EDRF1 +110 more	Copy number gain	not provided	GPathogenic
Select item 1172570	GRCh37/hg19 10q26.12-26.3(chr10:122785023-135457222)x1	FANK1, FGFR2 +79 more	Copy number loss	See cases	GPathogenic
Select item 815379	GRCh37/hg19 10q26.11-26.3(chr10:119996339-135427143)x3	FGFR2, FOXI2 +95 more	Copy number gain	not provided	GPathogenic
Select item 779127	NM_005519.2(HMX2):c.665C>G (p.Ala222Gly)	HMX2, LOC124416925 (A222G)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 747916	NM_005519.2(HMX2):c.579A>G (p.Val193=)	HMX2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 747915	NM_005519.2(HMX2):c.303C>A (p.Gly101=)	HMX2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 687114	GRCh37/hg19 10q25.2-26.3(chr10:114544537-135427143)x3	ABLIM1, ABRAXAS2 +130 more	Copy number gain	not provided	GPathogenic
Select item 625657	GRCh37/hg19 10q25.1-26.3(chr10:110022170-135439095)	ABLIM1, ABRAXAS2 +146 more	Copy number gain	not provided	GPathogenic
Select item 625556	GRCh37/hg19 10q25.3-26.13(chr10:117024753-124942806)	ACADSB, ARMS2 +54 more	Copy number loss	Distal 10q deletion syndrome	GPathogenic
Select item 623448	NM_005519.2(HMX2):c.269-1G>A	HMX2	Single nucleotide variant (splice acceptor variant)	High myopia	GUncertain significance
Select item 563802	GRCh37/hg19 10q23.33-26.3(chr10:94346520-135427143)x3	ABCC2, ABLIM1 +298 more	Copy number gain	not provided	GPathogenic
Select item 563801	GRCh37/hg19 10q24.33-26.3(chr10:105613040-135427143)x3	ABLIM1, ABRAXAS2 +157 more	Copy number gain	not provided	GPathogenic
Select item 563799	GRCh37/hg19 10q26.11-26.3(chr10:121269222-135427143)x3	ABRAXAS2, ACADSB +86 more	Copy number gain	not provided	GPathogenic
Select item 563798	GRCh37/hg19 10q26.12-26.3(chr10:122509781-135427143)x1	ABRAXAS2, ACADSB +79 more	Copy number loss	not provided	GPathogenic
Select item 563797	GRCh37/hg19 10q26.12-26.3(chr10:123019239-135427143)x1	ABRAXAS2, ACADSB +78 more	Copy number loss	not provided	GPathogenic
Select item 563690	GRCh37/hg19 10q26.13(chr10:124858722-124916708)x1	BUB3, HMX3 +1 more	Copy number loss	not provided	GUncertain significance
Select item 523165	GRCh37/hg19 10q11.21-26.3(chr10:42347406-135534747)x1	COX15, CPEB3 +569 more	Copy number loss	Poly (ADP-Ribose) polymerase inhibitor response	Gdrug response
Select item 443838	GRCh37/hg19 10q25.1-26.3(chr10:106003533-135427143)x3	ABLIM1, ABRAXAS2 +151 more	Copy number gain	See cases	GPathogenic
Select item 443323	GRCh37/hg19 10q23.32-26.3(chr10:93283493-135427143)x3	ABCC2, ABLIM1 +305 more	Copy number gain	See cases	GPathogenic
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 395627	GRCh37/hg19 10q26.13-26.3(chr10:124147428-135370736)x1	ABRAXAS2, ACADSB +73 more	Copy number loss	See cases	GPathogenic
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 253890	GRCh37/hg19 10q26.13(chr10:124593422-125010666)x3	HMX2, FAM24A +8 more	Copy number gain	See cases	GUncertain significance
Select item 253479	GRCh37/hg19 10q24.32-26.3(chr10:103288313-135512075)x3	ABLIM1, ABRAXAS2 +201 more	Copy number gain	See cases	GPathogenic
Select item 253439	GRCh37/hg19 10q26.12-26.2(chr10:122239239-128203032)x1	C10orf90, CHST15 +40 more	Copy number loss	See cases	GPathogenic
Select item 219035	GRCh37/hg19 10q26.13-26.3(chr10:123731209-135353867)x1	ACADSB, ADAM12 +75 more	Copy number loss	See cases	GPathogenic
Select item 154670	GRCh38/hg38 10q26.13-26.3(chr10:121918547-133620674)x1	LOC130004911, LOC130004912 +395 more	Copy number loss	See cases	GPathogenic
Select item 154374	GRCh38/hg38 10q26.13-26.3(chr10:121588992-133620674)x1	FUOM, GLRX3 +399 more	Copy number loss	See cases	GPathogenic
Select item 153718	GRCh38/hg38 10q26.11-26.3(chr10:119707856-133613639)x3	LOC130004884, LOC130004885 +438 more	Copy number gain	See cases	GPathogenic
Select item 150986	GRCh38/hg38 10q26.13(chr10:122143176-124358013)x1	ACADSB, ARMS2 +81 more	Copy number loss	See cases	GPathogenic
Select item 150499	GRCh38/hg38 10q26.12-26.3(chr10:120970558-133622588)x1	LOC130005014, LOC130005015 +409 more	Copy number loss	See cases	GPathogenic
Select item 149417	GRCh38/hg38 10q26.13-26.3(chr10:122881207-133620609)x1	LOC130004994, LOC130004995 +361 more	Copy number loss	See cases	GPathogenic
Select item 148679	GRCh38/hg38 10q24.31-26.3(chr10:100600492-133622588)x3	GSTO1, GSTO2 +1097 more	Copy number gain	See cases	GPathogenic
Select item 144206	GRCh38/hg38 10q25.1-26.3(chr10:108102587-133620674)x3	LOC126861107, LOC128598885 +802 more	Copy number gain	See cases	GPathogenic
Select item 59728	GRCh38/hg38 10q26.11-26.3(chr10:117866565-133554210)x3	ABRAXAS2, ACADSB +514 more	Copy number gain	See cases	GPathogenic
Select item 59707	GRCh38/hg38 10q24.31-26.3(chr10:100194215-132432797)x3	EDRF1-AS1, EDRF1-DT +1036 more	Copy number gain	See cases	GPathogenic
Select item 58821	GRCh38/hg38 10q26.13-26.2(chr10:122973296-128210291)x1	ABRAXAS2, ACADSB +182 more	Copy number loss	See cases	GPathogenic
Select item 58820	GRCh38/hg38 10q26.13-26.2(chr10:122826743-126730948)x1	ABRAXAS2, ACADSB +164 more	Copy number loss	See cases	GPathogenic
Select item 57507	GRCh38/hg38 10q25.2-26.3(chr10:111313099-133620674)x3	ABLIM1, ABRAXAS2 +679 more	Copy number gain	See cases	GPathogenic
Select item 57403	GRCh38/hg38 10q26.12-26.3(chr10:120454430-133620674)x1	LOC130004881, LOC130004882 +418 more	Copy number loss	See cases	GPathogenic
Select item 57376	GRCh38/hg38 10q26.13-26.3(chr10:122265252-133620674)x1	ABRAXAS2, ACADSB +383 more	Copy number loss	See cases	GPathogenic

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Links from Gene

Items: 78