2762[Gene ID] - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 58124	GRCh38/hg38 6p25.3-22.3(chr6:106431-18360595)x3	LINC02522, LINC02525 +823 more	Copy number gain	See cases	GPathogenic
Select item 58405	GRCh38/hg38 6p25.3-25.1(chr6:107682-4978781)x1	BPHL, C6orf201 +258 more	Copy number loss	See cases	GPathogenic
Select item 58125	GRCh38/hg38 6p25.3-25.1(chr6:144957-5239181)x3	BPHL, C6orf201 +279 more	Copy number gain	See cases	GPathogenic
Select item 155267	GRCh38/hg38 6p25.3-23(chr6:152634-14417003)x3	LOC132089500, LOC132090749 +641 more	Copy number gain	See cases	GPathogenic
Select item 154849	GRCh38/hg38 6p25.3-25.1(chr6:152634-6289804)x1	BPHL, C6orf201 +312 more	Copy number loss	See cases	GPathogenic
Select item 149755	GRCh38/hg38 6p25.3-25.1(chr6:152634-6027547)x1	BPHL, C6orf201 +307 more	Copy number loss	See cases	GPathogenic
Select item 149754	GRCh38/hg38 6p25.3-25.1(chr6:152634-6027547)x3	LOC129995684, LOC129995685 +307 more	Copy number gain	See cases	GLikely pathogenic
Select item 148422	GRCh38/hg38 6p25.3-25.1(chr6:152634-5315679)x1	LOC129995551, LOC129995552 +287 more	Copy number loss	See cases	GPathogenic
Select item 151603	GRCh38/hg38 6p25.3-22.3(chr6:155807-17058414)x3	LOC129995714, LOC129995715 +777 more	Copy number gain	See cases	GPathogenic
Select item 155715	GRCh38/hg38 6p25.3-23(chr6:156974-13855925)x1	LOC129995520, LOC129995521 +610 more	Copy number loss	See cases	GPathogenic
Select item 155631	GRCh38/hg38 6p25.3-24.1(chr6:156974-13081201)x3	LOC121106426, LOC121113497 +557 more	Copy number gain	See cases	GLikely pathogenic
Select item 155430	GRCh38/hg38 6p25.3-12.3(chr6:156974-46789291)x3	CYP39A1, DAAM2 +2577 more	Copy number gain	See cases	GPathogenic
Select item 155308	GRCh38/hg38 6p25.3-25.1(chr6:156974-4946857)x3	BPHL, C6orf201 +255 more	Copy number gain	See cases	GUncertain significance
Select item 154201	GRCh38/hg38 6p25.3-25.1(chr6:156974-4907692)x1	LOC121740636, LOC121740637 +255 more	Copy number loss	See cases	GPathogenic
Select item 154194	GRCh38/hg38 6p25.3-24.3(chr6:156974-7122759)x1	LOC123575649, LOC123575650 +345 more	Copy number loss	See cases	GPathogenic
Select item 154190	GRCh38/hg38 6p25.3-24.2(chr6:156974-11550817)x3	LINC02521, LINC02522 +508 more	Copy number gain	See cases	GLikely pathogenic
Select item 149126	GRCh38/hg38 6p25.3-25.2(chr6:163083-3459607)x1	BPHL, DUSP22 +211 more	Copy number loss	See cases	GPathogenic
Select item 147369	GRCh38/hg38 6p25.3-24.3(chr6:163083-9525496)x3	BLOC1S5, BLOC1S5-TXNDC5 +435 more	Copy number gain	See cases	GPathogenic
Select item 146312	GRCh38/hg38 6p25.3(chr6:163083-2029531)x3	DUSP22, EXOC2 +118 more	Copy number gain	See cases	GPathogenic
Select item 58408	GRCh38/hg38 6p25.3-25.2(chr6:163083-2724611)x1	DUSP22, EXOC2 +127 more	Copy number loss	See cases	GPathogenic
Select item 58407	GRCh38/hg38 6p25.3-25.1(chr6:163083-5875402)x1	LOC129389427, LOC129389428 +301 more	Copy number loss	See cases	GPathogenic
Select item 57077	GRCh38/hg38 6p25.3-25.1(chr6:163083-6062800)x1	LOC126859547, LOC126859548 +305 more	Copy number loss	See cases	GPathogenic
Select item 57019	GRCh38/hg38 6p25.3(chr6:163083-1951351)x3	LOC129995574, LOC129995575 +116 more	Copy number gain	See cases	GPathogenic
Select item 144540	GRCh38/hg38 6p25.3-24.1(chr6:164360-13339881)x3	LOC129995778, LOC129995779 +571 more	Copy number gain	See cases	GPathogenic
Select item 58410	GRCh38/hg38 6p25.3-25.1(chr6:164633-5823601)x1	BPHL, C6orf201 +300 more	Copy number loss	See cases	GPathogenic
Select item 58409	GRCh38/hg38 6p25.3-25.1(chr6:164633-6284237)x1	LOC129995595, LOC129995596 +310 more	Copy number loss	See cases	GPathogenic
Select item 58411	GRCh38/hg38 6p25.3-24.3(chr6:165675-9036034)x1	LOC126859546, LOC126859547 +431 more	Copy number loss	See cases	GPathogenic
Select item 58150	GRCh38/hg38 6p25.3-23(chr6:389423-13474956)x3	LOC129995630, LOC129995631 +536 more	Copy number gain	See cases	GPathogenic
Select item 154994	GRCh38/hg38 6p25.3(chr6:1365202-1627578)x3	FOXC1, FOXCUT +13 more	Copy number gain	See cases	GUncertain significance
Select item 146401	GRCh38/hg38 6p25.3-25.2(chr6:1441186-2351374)x1	FOXC1, FOXCUT +19 more	Copy number loss	See cases	GPathogenic
Select item 58421	GRCh38/hg38 6p25.3-25.2(chr6:1490636-2700006)x1	FOXC1, FOXCUT +24 more	Copy number loss	See cases	GPathogenic
Select item 150317	GRCh38/hg38 6p25.3-25.2(chr6:1490637-2677489)x3	FOXC1, FOXCUT +24 more	Copy number gain	See cases	GUncertain significance
Select item 144141	GRCh38/hg38 6p25.3(chr6:1580446-1951292)x1	FOXC1, FOXCUT +12 more	Copy number loss	See cases	GPathogenic
Select item 58422	GRCh38/hg38 6p25.3(chr6:1605533-1739699)x1	FOXC1, FOXCUT +7 more	Copy number loss	See cases	GPathogenic
Select item 2495360	NM_001500.4(GMDS):c.874A>G (p.Ile292Val)	GMDS (I262V +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2656175	NM_001500.4(GMDS):c.804G>A (p.Pro268=)	GMDS	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2408958	NM_001500.4(GMDS):c.803C>T (p.Pro268Leu)	GMDS (P238L +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 148793	GRCh38/hg38 6p25.3(chr6:1744004-2006554)x1	GMDS, LOC126859553 +4 more	Copy number loss	See cases	GUncertain significance
Select item 155123	GRCh38/hg38 6p25.3(chr6:1768205-2246547)x1	GMDS, GMDS-DT +8 more	Copy number loss	See cases	GUncertain significance
Select item 59496	GRCh38/hg38 6p25.3-25.2(chr6:1796838-2854327)x3	GMDS, GMDS-DT +28 more	Copy number gain	See cases	GUncertain significance
Select item 153811	GRCh38/hg38 6p25.3-25.2(chr6:1943429-2507158)x3	GMDS, GMDS-DT +6 more	Copy number gain	See cases	GLikely benign
Select item 2485843	NM_001500.4(GMDS):c.554A>G (p.Tyr185Cys)	GMDS (Y155C +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2496172	NM_001500.4(GMDS):c.389T>C (p.Val130Ala)	GMDS (V100A +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2618510	NM_001500.4(GMDS):c.362C>T (p.Ala121Val)	GMDS (A121V +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2275169	NM_001500.4(GMDS):c.166C>T (p.Arg56Trp)	GMDS (R56W +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2296254	NM_001500.4(GMDS):c.163C>T (p.Arg55Trp)	GMDS (R25W +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2479158	NM_001500.4(GMDS):c.26C>T (p.Pro9Leu)	GMDS (P9L)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3062932	GRCh37/hg19 6p25.3-25.1(chr6:156974-4338899)x1	BPHL, C6orf201 +25 more	Copy number loss	not specified	GPathogenic
Select item 3062928	GRCh37/hg19 6p25.3-25.2(chr6:156974-3175378)x3	BPHL, DUSP22 +16 more	Copy number gain	not specified	GPathogenic
Select item 3062921	GRCh37/hg19 6p25.3-25.2(chr6:1479303-2693757)x3	FOXC1, GMDS +2 more	Copy number gain	not specified	GUncertain significance
Select item 3062906	GRCh37/hg19 6p25.3(chr6:1562445-1646030)x1	FOXC1, GMDS	Copy number loss	not specified	GPathogenic
Select item 3062879	GRCh37/hg19 6p25.3(chr6:1527438-2021057)x3	FOXC1, GMDS	Copy number gain	not specified	GUncertain significance
Select item 3062878	GRCh37/hg19 6p25.3(chr6:1593074-1660677)x3	FOXC1, GMDS	Copy number gain	not specified	GUncertain significance
Select item 2685193	GRCh37/hg19 6p25.3(chr6:647204-1716710)x1	EXOC2, FOXC1 +4 more	Copy number loss	not provided	GPathogenic
Select item 2685192	GRCh37/hg19 6p25.3(chr6:156975-2072578)x1	DUSP22, EXOC2 +6 more	Copy number loss	not provided	GPathogenic
Select item 2684440	GRCh37/hg19 6p25.3(chr6:1286450-1645873)x3	FOXC1, FOXF2 +2 more	Copy number gain	not provided	GLikely pathogenic
Select item 2684439	GRCh37/hg19 6p25.3-22.3(chr6:156975-15478095)x3	ADTRP, BLOC1S5 +73 more	Copy number gain	not provided	GPathogenic
Select item 2571270	GRCh37/hg19 6p25.3-25.2(chr6:393153-3751765)x1	SERPINB9, TUBB2A +19 more	Copy number loss	not provided	GPathogenic
Select item 2506536	GRCh37/hg19 6p25.3(chr6:491126-1624775)	EXOC2, FOXC1 +4 more	Copy number loss	Axenfeld-Rieger syndrome type 3	GPathogenic
Select item 1810398	GRCh37/hg19 6p25.3-22.3(chr6:820000-21700000)x3	ADTRP, ATXN1 +89 more	Copy number gain	See cases	GPathogenic
Select item 1808989	GRCh37/hg19 6p25.3(chr6:1916017-2150008)x1	GMDS	Copy number loss	not provided	GUncertain significance
Select item 1808724	GRCh37/hg19 6p25.3-25.2(chr6:156975-3718881)x1	BPHL, DUSP22 +19 more	Copy number loss	not provided	GPathogenic
Select item 1808377	GRCh37/hg19 6p25.3-25.2(chr6:2162500-2864248)x3	GMDS, LINC01600 +3 more	Copy number gain	not provided	GUncertain significance
Select item 1676308	GRCh37/hg19 6p25.3-25.2(chr6:375263-3655142)x1	BPHL, EXOC2 +18 more	Copy number loss	Axenfeld-Rieger syndrome type 3	GPathogenic
Select item 1527214	GRCh37/hg19 6p25.3(chr6:1527437-1764940)	FOXC1, GMDS	Copy number gain	not specified	GUncertain significance
Select item 1527212	GRCh37/hg19 6p25.3-25.2(chr6:383951-3898619)	BPHL, EXOC2 +20 more	Copy number loss	not specified	GPathogenic
Select item 1340917	GRCh37/hg19 6p25.3(chr6:1440644-1695652)x3	FOXC1, GMDS	Copy number gain	not provided	GUncertain significance
Select item 1340497	GRCh37/hg19 6p25.3(chr6:1705438-1767134)x1	GMDS	Copy number loss	not provided	GUncertain significance
Select item 1340369	GRCh37/hg19 6p25.3(chr6:1397495-1927651)x3	FOXC1, GMDS	Copy number gain	not provided	GUncertain significance
Select item 1180550	GRCh37/hg19 6p25.3-25.2(chr6:149619-3951208)x3	BPHL, DUSP22 +21 more	Copy number gain	not provided	GPathogenic
Select item 983174	GRCh37/hg19 6p25.3(chr6:152849-1888703)x1	FOXC1, FOXF2 +6 more	Copy number loss	See cases	GPathogenic
Select item 980203	GRCh37/hg19 6p25.3-25.2(chr6:302183-3290583)x3	TUBB2A, DUSP22 +19 more	Copy number gain	not provided	GPathogenic
Select item 980202	GRCh37/hg19 6p25.3-25.2(chr6:2094762-2376301)x3	GMDS	Copy number gain	not provided	GLikely benign
Select item 973777	GRCh37/hg19 6p25.3(chr6:1347995-1713458)x3	FOXC1, FOXF2 +2 more	Copy number gain	Late onset congenital glaucoma	GPathogenic
Select item 973776	GRCh37/hg19 6p25.3(chr6:1318643-1837594)x3	FOXC1, FOXF2 +2 more	Copy number gain	Anterior segment dysgenesis 3	GPathogenic
Select item 814773	GRCh37/hg19 6p25.3-25.2(chr6:2167407-2775133)x3	WRNIP1, MYLK4 +2 more	Copy number gain	not provided	GUncertain significance
Select item 814772	GRCh37/hg19 6p25.3-25.2(chr6:2058918-2362369)x3	GMDS	Copy number gain	not provided	GLikely benign
Select item 814771	GRCh37/hg19 6p25.3(chr6:1949490-1999263)x1	GMDS	Copy number loss	not provided	GUncertain significance
Select item 814767	GRCh37/hg19 6p25.3(chr6:156974-2208360)x1	HUS1B, EXOC2 +6 more	Copy number loss	not provided	GPathogenic
Select item 813838	GRCh37/hg19 6p25.3(chr6:1989529-2084356)x1	GMDS	Copy number loss	Intellectual disability +1 more	GUncertain significance
Select item 688851	GRCh37/hg19 6p25.3-25.2(chr6:2129442-2500820)x3	GMDS	Copy number gain	not provided	GUncertain significance
Select item 687645	GRCh37/hg19 6p25.3(chr6:2113808-2188830)x1	GMDS	Copy number loss	not provided	GUncertain significance
Select item 687409	GRCh37/hg19 6p25.3-22.3(chr6:156974-23221621)x3	ADTRP, ATXN1 +95 more	Copy number gain	not provided	GPathogenic
Select item 687230	GRCh37/hg19 6p25.3(chr6:1910715-2150669)x1	GMDS	Copy number loss	not provided	GUncertain significance
Select item 563147	GRCh37/hg19 6p25.3-25.2(chr6:2162499-2624262)x3	LINC01600, GMDS	Copy number gain	not provided	GUncertain significance
Select item 563146	GRCh37/hg19 6p25.3-25.2(chr6:1920928-2489477)x3	GMDS	Copy number gain	not provided	GLikely benign
Select item 563145	GRCh37/hg19 6p25.3(chr6:1875823-1964471)x1	GMDS	Copy number loss	not provided	GUncertain significance
Select item 563144	GRCh37/hg19 6p25.3-24.3(chr6:1860928-8884071)x3	BLOC1S5, BMP6 +38 more	Copy number gain	not provided	GLikely pathogenic
Select item 563140	GRCh37/hg19 6p25.3-22.3(chr6:156974-21955964)x3	ADTRP, ATXN1 +93 more	Copy number gain	not provided	GPathogenic
Select item 563139	GRCh37/hg19 6p25.3-23(chr6:156974-13502033)x3	ADTRP, BLOC1S5 +66 more	Copy number gain	not provided	GPathogenic
Select item 563138	GRCh37/hg19 6p25.3-25.2(chr6:156974-3398920)x1	HUS1B, SERPINB6 +19 more	Copy number loss	not provided	GPathogenic
Select item 560067	Single allele	ADTRP, ATXN1 +95 more	Duplication	not provided	GPathogenic
Select item 443604	GRCh37/hg19 6p25.3(chr6:1703078-1918006)x1	GMDS	Copy number loss	See cases	GLikely pathogenic
Select item 443497	GRCh37/hg19 6p25.3-q27(chr6:156975-170919482)	AIRN, BNIP5 +1028 more	Copy number gain	See cases	GPathogenic
Select item 443496	GRCh37/hg19 6p25.3-q27(chr6:156975-170919482)x3	PDE10A, PDE7B +1028 more	Copy number gain	See cases	GPathogenic
Select item 443199	GRCh37/hg19 6p25.3-25.2(chr6:383951-4183288)x1	BPHL, C6orf201 +24 more	Copy number loss	See cases	GPathogenic
Select item 442601	GRCh37/hg19 6p25.3(chr6:195229-2117379)x1	DUSP22, EXOC2 +6 more	Copy number loss	See cases	GPathogenic
Select item 442393	GRCh37/hg19 6p25.3-25.1(chr6:156974-6417749)x1	BPHL, C6orf201 +33 more	Copy number loss	See cases	GPathogenic
Select item 442040	GRCh37/hg19 6p25.3-25.1(chr6:2109893-5962832)x1	BPHL, C6orf201 +24 more	Copy number loss	See cases	GPathogenic
Select item 441966	GRCh37/hg19 6p25.3(chr6:1305572-1825339)x3	FOXC1, FOXF2 +2 more	Copy number gain	See cases	GUncertain significance

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