UTP23[gene] - ClinVar

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Items: 78

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 153413	GRCh38/hg38 8p23.3-q24.3(chr8:208048-145070385)x3	LOC126860438, LOC126860439 +3663 more	Copy number gain	See cases	GPathogenic
Select item 154791	GRCh38/hg38 8p23.3-q24.3(chr8:226452-145068712)x3	AARD, ABRA +3663 more	Copy number gain	See cases	GPathogenic
Select item 59738	GRCh38/hg38 8p23.3-q24.3(chr8:241530-145054634)x3	AARD, ABRA +3661 more	Copy number gain	See cases	GPathogenic
Select item 57496	GRCh38/hg38 8p23.3-q24.3(chr8:241530-145049449)x3	LOC105379224, LOC105379230 +3657 more	Copy number gain	See cases	GPathogenic
Select item 149660	GRCh38/hg38 8p23.3-q24.3(chr8:241605-145054781)x3	AARD, ABRA +3661 more	Copy number gain	See cases	GPathogenic
Select item 153737	GRCh38/hg38 8p21.3-q24.3(chr8:21291522-145070385)x3	LOC129999966, LOC129999967 +3111 more	Copy number gain	See cases	GPathogenic
Select item 150723	GRCh38/hg38 8q11.1-24.3(chr8:46031340-139285494)x3	LOC126860489, LOC126860490 +1963 more	Copy number gain	See cases	GPathogenic
Select item 150141	GRCh38/hg38 8q21.13-24.3(chr8:77480050-145068712)x3	AARD, ABRA +1691 more	Copy number gain	See cases	GPathogenic
Select item 154530	GRCh38/hg38 8q21.13-24.3(chr8:78614077-145054634)x3	LOC126860535, LOC126860536 +1687 more	Copy number gain	See cases	GPathogenic
Select item 155592	GRCh38/hg38 8q21.2-24.3(chr8:85765999-145070385)x3	LOC105375713, LOC105375742 +1553 more	Copy number gain	See cases	GPathogenic
Select item 146316	GRCh38/hg38 8q21.3-24.23(chr8:86300584-137022587)x3	AARD, ABRA +1153 more	Copy number gain	See cases	GPathogenic
Select item 149554	GRCh38/hg38 8q21.3-24.3(chr8:87931152-145068712)x3	LOC130001109, LOC130001110 +1532 more	Copy number gain	See cases	GPathogenic
Select item 144949	GRCh38/hg38 8q22.1-24.3(chr8:94682154-145068656)x3	LOC130001226, LOC130001227 +1407 more	Copy number gain	See cases	GPathogenic
Select item 151754	GRCh38/hg38 8q22.1-24.3(chr8:97382873-145070385)x3	AARD, ABRA +1330 more	Copy number gain	See cases	GPathogenic
Select item 153231	GRCh38/hg38 8q22.3-24.3(chr8:100867343-145070385)x3	LOC130000987, LOC130000988 +1205 more	Copy number gain	See cases	GPathogenic
Select item 154743	GRCh38/hg38 8q22.3-24.3(chr8:103306336-145068712)x3	LOC130001173, LOC130001174 +1068 more	Copy number gain	See cases	GPathogenic
Select item 146552	GRCh38/hg38 8q23.3-24.12(chr8:112528342-120083041)x1	LOC110120802, LOC111556135 +93 more	Copy number loss	See cases	GPathogenic
Select item 60403	GRCh38/hg38 8q23.3-24.21(chr8:113288454-126716087)x1	AARD, ANXA13 +315 more	Copy number loss	See cases	GPathogenic
Select item 145965	GRCh38/hg38 8q23.3-24.12(chr8:113418060-120975305)x1	MTBP, RAD21 +101 more	Copy number loss	See cases	GPathogenic
Select item 57045	GRCh38/hg38 8q23.3-24.3(chr8:113580402-145054634)x3	LOC130001070, LOC130001071 +962 more	Copy number gain	See cases	GPathogenic
Select item 152006	GRCh38/hg38 8q23.3-24.13(chr8:113933305-122621741)x1	AARD, CCN3 +108 more	Copy number loss	See cases	GPathogenic
Select item 150131	GRCh38/hg38 8q23.3-24.13(chr8:114560780-122594102)x1	AARD, CCN3 +106 more	Copy number loss	See cases	GPathogenic
Select item 2579176	GRCh38/hg38 8q23.3-24.23(chr8:115586904-135607135)x3	LOC130001241, LOC130001242 +559 more	Copy number gain	Neurodevelopmental disorder	GPathogenic
Select item 154486	GRCh38/hg38 8q23.3-24.11(chr8:116497730-117379167)x1	AARD, EIF3H +19 more	Copy number loss	See cases	GUncertain significance
Select item 2552471	NM_032334.3(UTP23):c.8T>A (p.Ile3Asn)	LOC130000991, UTP23 (I3N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3331743	NM_032334.3(UTP23):c.36T>G (p.His12Gln)	LOC130000991, UTP23 (H12Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2361479	NM_032334.3(UTP23):c.161T>G (p.Met54Arg)	LOC130000991, UTP23 (M54R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2303626	NM_032334.3(UTP23):c.266G>A (p.Arg89Gln)	UTP23 (R89Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2291972	NM_032334.3(UTP23):c.323T>C (p.Val108Ala)	UTP23 (V108A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2211831	NM_032334.3(UTP23):c.353T>C (p.Val118Ala)	UTP23 (V118A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2395247	NM_032334.3(UTP23):c.394A>C (p.Lys132Gln)	UTP23 (K132Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2491522	NM_032334.3(UTP23):c.428A>T (p.Asn143Ile)	UTP23 (N143I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 776379	NM_032334.3(UTP23):c.509A>G (p.His170Arg)	UTP23 (H170R)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 3187957	NM_032334.3(UTP23):c.524T>C (p.Ile175Thr)	UTP23 (I175T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2460349	NM_032334.3(UTP23):c.527A>G (p.Lys176Arg)	UTP23 (K176R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2404270	NM_032334.3(UTP23):c.538G>C (p.Glu180Gln)	UTP23 (E180Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3331744	NM_032334.3(UTP23):c.543A>T (p.Glu181Asp)	UTP23 (E181D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2307698	NM_032334.3(UTP23):c.640G>T (p.Ala214Ser)	UTP23 (A214S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1287707	NM_032334.3(UTP23):c.644C>T (p.Pro215Leu)	UTP23 (P215L)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 3187958	NM_032334.3(UTP23):c.728A>G (p.Lys243Arg)	UTP23 (K243R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3245563	NC_000008.10:g.(?_116426251)_(119965024_?)del	AARD, EIF3H +9 more	Deletion	not provided	GPathogenic
Select item 3245509	NC_000008.10:g.(?_116426251)_(120844804_?)del	CCN3, AARD +14 more	Deletion	Trichorhinophalangeal syndrome, type III +1 more	GPathogenic
Select item 3245404	NC_000008.10:g.(?_116426251)_(120844804_?)dup	AARD, CCN3 +14 more	Duplication	Trichorhinophalangeal syndrome, type III +2 more	GUncertain significance
Select item 3063013	GRCh37/hg19 8p23.3-q24.3(chr8:158048-146295771)x3	AARD, ABRA +665 more	Copy number gain	not specified	GPathogenic
Select item 3024645	GRCh37/hg19 8q23.3-24.3(chr8:113392581-146364022)x3	NRBP2, NSMCE2 +173 more	Copy number gain	not provided	GPathogenic
Select item 2422394	NC_000008.10:g.(?_117647788)_(120797526_?)dup	AARD, CCN3 +12 more	Duplication	Multiple congenital exostosis	GUncertain significance
Select item 1809294	GRCh37/hg19 8q23.3-24.11(chr8:117617532-117862147)x3	EIF3H, RAD21 +1 more	Copy number gain	not provided	GUncertain significance
Select item 1808708	GRCh37/hg19 8q23.3-24.22(chr8:112234557-133668379)x1	AARD, ADCY8 +63 more	Copy number loss	not provided	GPathogenic
Select item 1808681	GRCh37/hg19 8q21.12-24.11(chr8:79409349-119040631)x3	AARD, ABRA +141 more	Copy number gain	not provided	GPathogenic
Select item 1711167	GRCh37/hg19 8q13.2-24.3(chr8:68912432-146295771)x2	AARD, ABRA +335 more	Copy number gain	See cases	GPathogenic
Select item 1706511	GRCh37/hg19 8q21.2-24.3(chr8:84712253-146295771)x3	AARD, ABRA +285 more	Copy number gain	See cases	GPathogenic
Select item 1703544	GRCh37/hg19 8p23.3-q24.3(chr8:158048-146295771)	AARD, ABRA +665 more	Copy number gain	Polydactyly	GPathogenic
Select item 1676301	GRCh37/hg19 8q22.1-24.3(chr8:96496503-146295711)	FZD6, PCAT1 +236 more	Copy number gain	not provided	GPathogenic
Select item 1527464	GRCh37/hg19 8q23.3-24.11(chr8:117623123-117862147)	EIF3H, RAD21 +1 more	Copy number gain	not specified	GUncertain significance
Select item 1527461	GRCh37/hg19 8q23.1-24.12(chr8:107032887-120742018)	AARD, ABRA +28 more	Copy number loss	not specified	GPathogenic
Select item 1527440	GRCh37/hg19 8q13.2-24.3(chr8:70382990-146295771)	DCAF4L2, DCSTAMP +333 more	Copy number gain	not specified	GPathogenic
Select item 1444166	NC_000008.10:g.(?_117574515)_(117878968_?)dup	EIF3H, RAD21 +1 more	Duplication	Cornelia de Lange syndrome 4	GUncertain significance
Select item 1341181	GRCh37/hg19 8q23.3-24.11(chr8:117255161-118322087)x3	AARD, EIF3H +4 more	Copy number gain	not provided	GUncertain significance
Select item 1341025	GRCh37/hg19 8q23.3-24.11(chr8:117546387-117871814)x3	EIF3H, RAD21 +1 more	Copy number gain	not provided	GUncertain significance
Select item 979849	GRCh37/hg19 8q23.1-24.13(chr8:108421573-123429638)x3	AARD, ANGPT1 +35 more	Copy number gain	not provided	GPathogenic
Select item 815154	GRCh37/hg19 8q23.2-24.13(chr8:111514791-123192373)x1	AARD, CCN3 +23 more	Copy number loss	not provided	GPathogenic
Select item 687787	GRCh37/hg19 8p23.3-q24.3(chr8:158048-146295771)x3	BAALC, CNOT7 +665 more	Copy number gain	not provided	GPathogenic
Select item 687493	GRCh37/hg19 8p12-q24.3(chr8:31936551-146295771)x3	HSF1, HTRA4 +474 more	Copy number gain	not provided	GPathogenic
Select item 599306	Single allele	PCAT1, POU5F1B +52 more	Deletion	Trichorhinophalangeal dysplasia type I	GPathogenic
Select item 563549	GRCh37/hg19 8q23.1-24.13(chr8:110250943-123515785)x1	AARD, CCN3 +29 more	Copy number loss	not provided	GPathogenic
Select item 563463	GRCh37/hg19 8q23.3-24.11(chr8:117623123-117862147)x3	RAD21, EIF3H +1 more	Copy number gain	not provided	GUncertain significance
Select item 443924	GRCh37/hg19 8q21.2-24.3(chr8:86841154-146295771)x3	AARD, ABRA +277 more	Copy number gain	See cases	GPathogenic
Select item 443619	GRCh37/hg19 8p23.1-q24.3(chr8:12490999-146295771)x3	AARD, ABRA +593 more	Copy number gain	See cases	GPathogenic
Select item 442692	GRCh37/hg19 8q23.3-24.3(chr8:114853126-146295771)x3	AARD, ADCK5 +172 more	Copy number gain	See cases	GPathogenic
Select item 442201	GRCh37/hg19 8p23.3-q24.3(chr8:158049-146295771)x3	AARD, ABRA +665 more	Copy number gain	See cases	GPathogenic
Select item 442200	GRCh37/hg19 8p23.3-q24.3(chr8:158049-146295771)	FGF20, FGFR1 +665 more	Copy number gain	See cases	GPathogenic
Select item 441804	GRCh37/hg19 8q21.3-24.3(chr8:93047482-141355635)x3	RRM2B, SLC30A8 +160 more	Copy number gain	See cases	GPathogenic
Select item 441733	GRCh37/hg19 8q23.2-24.12(chr8:111137305-119897611)x1	AARD, CSMD3 +9 more	Copy number loss	See cases	GPathogenic
Select item 441594	GRCh37/hg19 8q21.2-24.3(chr8:86841228-142689874)x3	SLC45A4, SLC7A13 +189 more	Copy number gain	See cases	GPathogenic
Select item 395449	GRCh37/hg19 8q22.1-24.3(chr8:98432250-146222672)x4	AARD, ABRA +228 more	Copy number gain	See cases	GPathogenic
Select item 394884	GRCh37/hg19 8p23.3-q24.3(chr8:158991-146280828)x3	SCRT1, SCX +665 more	Copy number gain	See cases	GPathogenic
Select item 253883	GRCh37/hg19 8q23.3-24.11(chr8:117649533-117863721)x3	UTP23, RAD21 +1 more	Copy number gain	See cases	GUncertain significance
Select item 253639	GRCh37/hg19 8q24.11(chr8:117714768-119072307)x1	RAD21, UTP23 +5 more	Copy number loss	See cases	GPathogenic

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Items: 78