CNIH3[gene] - ClinVar

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Items: 52

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 153790	GRCh38/hg38 1q32.1-42.12(chr1:204764914-225408698)x3	LOC129388734, LOC129388735 +723 more	Copy number gain	See cases	GPathogenic
Select item 155660	GRCh38/hg38 1q32.2-44(chr1:207346642-248930485)x3	ABCB10, ACBD3 +1428 more	Copy number gain	See cases	GPathogenic
Select item 1809607	GRCh38/hg38 1q32.2-42.13(chr1:228006998-228061271)x2	LOC126806029, LOC129932471 +720 more	Copy number loss	Orofacial cleft 2	Gassociation
Select item 58116	GRCh38/hg38 1q32.2-44(chr1:209646207-248931113)x3	LOC120908923, LOC120947224 +1352 more	Copy number gain	See cases	GPathogenic
Select item 145652	GRCh38/hg38 1q32.2-44(chr1:209963625-248918469)x3	ABCB10, ACBD3 +1326 more	Copy number gain	See cases	GPathogenic
Select item 57302	GRCh38/hg38 1q32.3-44(chr1:214023812-248918469)x3	LOC129932855, LOC129932856 +1168 more	Copy number gain	See cases	GPathogenic
Select item 147449	GRCh38/hg38 1q41-42.13(chr1:223347693-228556332)x1	ACBD3, ACBD3-AS1 +287 more	Copy number loss	See cases	GPathogenic
Select item 57010	GRCh38/hg38 1q41-44(chr1:223347693-248918469)x3	TARBP1, TBCE +968 more	Copy number gain	See cases	GPathogenic
Select item 146036	GRCh38/hg38 1q41-42.12(chr1:223749425-224604271)x1	CAPN2, CNIH3 +40 more	Copy number loss	See cases	GUncertain significance
Select item 146575	GRCh38/hg38 1q41-44(chr1:223815147-248918469)x3	LINC02765, LINC02768 +955 more	Copy number gain	See cases	GPathogenic
Select item 58133	GRCh38/hg38 1q41-44(chr1:223828500-248891309)x3	LOC440742, LYPD8 +955 more	Copy number gain	See cases	GPathogenic
Select item 57169	GRCh38/hg38 1q41-42.12(chr1:223882252-224902629)x1	CNIH3, CNIH3-AS1 +43 more	Copy number loss	See cases	GUncertain significance
Select item 58135	GRCh38/hg38 1q41-44(chr1:223887780-248891309)x3	ABCB10, ACBD3 +953 more	Copy number gain	See cases	GPathogenic
Select item 148701	GRCh38/hg38 1q42.11-44(chr1:224022862-248918469)x3	LOC129932825, LOC129932826 +952 more	Copy number gain	See cases	GPathogenic
Select item 58137	GRCh38/hg38 1q42.11-44(chr1:224096488-248918469)x3	LOC129932658, LOC129932659 +950 more	Copy number gain	See cases	GPathogenic
Select item 2579189	GRCh38/hg38 1q42.11-42.12(chr1:224304638-224434886)x1	CNIH3, CNIH4 +12 more	Copy number loss	Skraban-Deardorff syndrome	GPathogenic
Select item 1879112	NC_000001.11:g.224435176C>G	CNIH3, WDR26 (Q30E)	Single nucleotide variant (missense variant +2 more)	not provided	GBenign
Select item 2639938	NC_000001.11:g.224454289T>C	CNIH3, WDR26	Single nucleotide variant (synonymous variant +2 more)	not provided	GBenign
Select item 2248358	NM_152495.2(CNIH3):c.16G>A (p.Ala6Thr)	CNIH3 (A6T)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2400408	NM_152495.2(CNIH3):c.68T>G (p.Phe23Cys)	CNIH3 (F23C)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2518609	NM_152495.2(CNIH3):c.104G>C (p.Arg35Thr)	CNIH3 (R63T +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3146472	NM_152495.2(CNIH3):c.116A>G (p.Lys39Arg)	CNIH3 (K21R +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2261398	NM_152495.2(CNIH3):c.142G>A (p.Val48Ile)	CNIH3 (V30I +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2243618	NM_152495.2(CNIH3):c.149C>A (p.Ala50Glu)	CNIH3 (A32E +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2550600	NM_152495.2(CNIH3):c.162G>C (p.Leu54Phe)	CNIH3 (L36F +3 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2508327	NM_152495.2(CNIH3):c.176G>A (p.Arg59His)	CNIH3 (R41H +3 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 154238	GRCh38/hg38 1q42.12(chr1:224722478-225761035)x1	CNIH3, CNIH3-AS1 +31 more	Copy number loss	See cases	GUncertain significance
Select item 2472981	NM_152495.2(CNIH3):c.376G>A (p.Asp126Asn)	CNIH3 (D110N +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3148877	GRCh37/hg19 1q41-42.12(chr1:216147522-226765691)x1	ACBD3, AIDA +53 more	Copy number loss	not provided	GPathogenic
Select item 1810315	GRCh37/hg19 1q42.11-43(chr1:224230307-243181599)x3	ABCB10, ACBD3 +113 more	Copy number gain	not provided	Gnot provided
Select item 1809372	GRCh37/hg19 1q41-44(chr1:223972939-249224684)x3	ABCB10, ACBD3 +185 more	Copy number gain	not provided	GPathogenic
Select item 1809014	GRCh37/hg19 1q41-42.12(chr1:221325488-225804228)x1	AIDA, BROX +21 more	Copy number loss	not provided	GUncertain significance
Select item 1708464	GRCh37/hg19 1q31.3-44(chr1:197867914-249224684)x3	COA6, COG2 +381 more	Copy number gain	See cases	GPathogenic
Select item 1703636	GRCh37/hg19 1q42.11-42.12(chr1:224432682-225142704)	CNIH3, CNIH4 +3 more	Copy number loss	Chromosome 1q41-q42 deletion syndrome	GPathogenic
Select item 1527559	GRCh37/hg19 1q41-42.13(chr1:221303919-227461343)	ACBD3, AIDA +38 more	Copy number gain	not specified	GPathogenic
Select item 1003645	NC_000001.10:g.(?_130980840)_(248900000_?)dup	FCGR3A, LCE3C +956 more	Duplication	Parathyroid carcinoma +2 more	GUncertain significance
Select item 929379	GRCh37/hg19 1q32.2-44(chr1:210152794-249218992)x3	CHML, CHRM3 +250 more	Copy number gain	See cases	GPathogenic
Select item 816482	GRCh37/hg19 1q32.1-44(chr1:204045948-249218992)x3	C1orf35, C1orf74 +320 more	Copy number gain	See cases	GPathogenic
Select item 814170	GRCh37/hg19 1q42.12(chr1:224702780-224838234)x3	CNIH3	Copy number gain	not provided	GUncertain significance
Select item 814169	GRCh37/hg19 1q42.12(chr1:224694958-225034105)x3	CNIH3	Copy number gain	not provided	GUncertain significance
Select item 814168	GRCh37/hg19 1q41-42.2(chr1:223653722-234591807)x1	FBXO28, ACBD3 +83 more	Copy number loss	not provided	GPathogenic
Select item 814166	GRCh37/hg19 1q41-42.13(chr1:222641389-228137574)x1	PSEN2, FBXO28 +42 more	Copy number loss	not provided	GPathogenic
Select item 814163	GRCh37/hg19 1q41-43(chr1:219916966-239004378)x3	CCDC185, NTPCR +127 more	Copy number gain	not provided	GPathogenic
Select item 685144	GRCh37/hg19 1q25.3-44(chr1:182388773-249111240)x3	C4BPB, CACNA1S +433 more	Copy number gain	not provided	GPathogenic
Select item 685030	GRCh37/hg19 1q42.11-42.12(chr1:224486843-225283297)x3	CNIH3, CNIH4 +3 more	Copy number gain	not provided	GUncertain significance
Select item 625540	GRCh37/hg19 1q42.11-42.12(chr1:224340881-225147932)	CNIH3, CNIH4 +5 more	Copy number loss	not provided	GPathogenic
Select item 565225	GRCh37/hg19 1q41-44(chr1:218252551-249224684)x3	H2BC26, H3-3A +213 more	Copy number gain	not provided	GPathogenic
Select item 442387	GRCh37/hg19 1p36.33-q44(chr1:849467-249224684)	CD34, CD46 +2014 more	Copy number gain	See cases	GPathogenic
Select item 442386	GRCh37/hg19 1p36.33-q44(chr1:849467-249224684)x3	GPATCH2, GPATCH3 +2014 more	Copy number gain	See cases	GPathogenic
Select item 441866	GRCh37/hg19 1q42.11-44(chr1:224105294-249224684)x3	ABCB10, ACBD3 +184 more	Copy number gain	See cases	GPathogenic
Select item 394081	GRCh37/hg19 1q31.3-44(chr1:195483439-249213000)x3	AVPR1B, B3GALNT2 +393 more	Copy number gain	See cases	GPathogenic
Select item 253654	GRCh37/hg19 1q31.3-42.13(chr1:197811907-228997888)x3	ACBD3, ADIPOR1 +242 more	Copy number gain	See cases	GPathogenic

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Items: 52