ClinVar for Gene (Select 85480) - ClinVar

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Links from Gene

Items: 50

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3329616	NM_033035.5(TSLP):c.445C>T (p.Arg149Cys)	TSLP (R149C +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3329615	NM_033035.5(TSLP):c.394G>C (p.Val132Leu)	TSLP (V36L +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3183756	NM_033035.5(TSLP):c.410G>C (p.Cys137Ser)	TSLP (C41S +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3062848	GRCh37/hg19 5q15-23.2(chr5:93828571-123711334)x1	AP3S1, APC +80 more	Copy number loss	not specified	GPathogenic
Select item 2685167	GRCh37/hg19 5q22.1(chr5:110371834-110456849)x1	TSLP, WDR36	Copy number loss	not provided	GUncertain significance
Select item 2685165	GRCh37/hg19 5q22.1(chr5:110328036-110438929)x1	TSLP, WDR36	Copy number loss	not provided	GUncertain significance
Select item 2671613	Single allele	CAMK4, EFNA5 +11 more	Deletion	not provided	GUncertain significance
Select item 2594703	NM_033035.5(TSLP):c.35T>A (p.Val12Asp)	TSLP (V12D)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2557352	NM_033035.5(TSLP):c.108T>G (p.Phe36Leu)	TSLP (F36L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2537567	NM_033035.5(TSLP):c.103G>A (p.Asp35Asn)	TSLP (D35N)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2499479	GRCh37/hg19 5q21.3-22.1(chr5:108634380-110629961)x3	CAMK4, MAN2A1 +5 more	Copy number gain	See cases	GUncertain significance
Select item 2496160	NM_033035.5(TSLP):c.203C>G (p.Ser68Cys)	TSLP (S68C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2400424	NM_033035.5(TSLP):c.418C>A (p.Gln140Lys)	TSLP (Q140K +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2370216	NM_033035.5(TSLP):c.181A>G (p.Thr61Ala)	TSLP (T61A)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2329524	NM_033035.5(TSLP):c.70G>C (p.Gly24Arg)	TSLP (G24R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2253341	NM_033035.5(TSLP):c.275C>G (p.Ser92Trp)	TSLP (S92W)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 1808130	GRCh37/hg19 5q22.1(chr5:109786744-110813071)x1	CAMK4, SLC25A46 +3 more	Copy number loss	not provided	GUncertain significance
Select item 1527183	GRCh37/hg19 5q21.1-23.2(chr5:100607918-125900735)	CAMK4, CCDC112 +60 more	Copy number loss	not specified	GPathogenic
Select item 1527179	GRCh37/hg19 5q15-22.3(chr5:93650000-114969108)	DCP2, EFNA5 +56 more	Copy number loss	not specified	GPathogenic
Select item 1340255	GRCh37/hg19 5q22.1(chr5:110299633-110427052)x1	TSLP	Copy number loss	not provided	GLikely benign
Select item 980177	GRCh37/hg19 5q22.1(chr5:110338499-110668272)x3	TSLP, WDR36 +1 more	Copy number gain	not provided	GUncertain significance
Select item 688598	GRCh37/hg19 5q14.3-23.3(chr5:89949118-129317455)x3	ADAMTS19, ADGRV1 +104 more	Copy number gain	not provided	GPathogenic
Select item 685538	GRCh37/hg19 5q21.3-23.1(chr5:108304806-121335239)x1	AP3S1, APC +39 more	Copy number loss	not provided	GPathogenic
Select item 635930	Single allele	C5orf24, C5orf34 +600 more	Deletion	Neurodevelopmental disorder	GUncertain significance
Select item 563100	GRCh37/hg19 5q22.1(chr5:110234471-110761241)x3	CAMK4, TSLP +1 more	Copy number gain	not provided	GUncertain significance
Select item 457359	NC_000005.9:g.(?_86400000)_(154000000_?)del	ARAP3, ARB2A +385 more	Deletion	Familial adenomatous polyposis 1 +1 more	GPathogenic
Select item 442882	GRCh37/hg19 5q21.3-22.1(chr5:108604653-110636716)x4	CAMK4, MAN2A1 +5 more	Copy number gain	See cases	GUncertain significance
Select item 442744	GRCh37/hg19 5q21.3-22.1(chr5:109146807-111474789)x4	CAMK4, MAN2A1 +6 more	Copy number gain	See cases	GUncertain significance
Select item 442431	GRCh37/hg19 5p15.1-q35.2(chr5:17628741-176575720)x1	DHFR, DHX29 +738 more	Copy number loss	See cases	GPathogenic
Select item 441920	GRCh37/hg19 5p15.33-q35.3(chr5:113577-180719789)	ABLIM3, ACOT12 +870 more	Copy number gain	See cases	GPathogenic
Select item 441919	GRCh37/hg19 5p15.33-q35.3(chr5:113577-180719789)x3	ABLIM3, ACOT12 +870 more	Copy number gain	See cases	GPathogenic
Select item 425542	GRCh37/hg19 5q15-35.3(chr5:94844077-178830410)x3	ARL10, ARL14EPL +511 more	Copy number gain	not provided	GLikely benign
Select item 395290	GRCh37/hg19 5q22.1-23.2(chr5:110407606-122522885)x1	TRIM36, TSLP +41 more	Copy number loss	See cases	GPathogenic
Select item 394550	GRCh37/hg19 5q21.3-35.3(chr5:106716357-180687338)x3	HRH2, HSD17B4 +520 more	Copy number gain	See cases	GPathogenic
Select item 253705	GRCh37/hg19 5q21.3-22.1(chr5:109438167-110644401)x3	WDR36, CAMK4 +3 more	Copy number gain	See cases	GUncertain significance
Select item 155679	GRCh38/hg38 5q14.3-31.1(chr5:91411708-131319563)x1	LOC126807500, LOC126807501 +689 more	Copy number loss	See cases	GPathogenic
Select item 155259	GRCh38/hg38 5q21.3-23.2(chr5:108308463-125777797)x1	LOC129994389, LOC129994390 +340 more	Copy number loss	See cases	GPathogenic
Select item 155182	GRCh38/hg38 5q15-22.2(chr5:93193104-113287795)x1	APC, ARB2A +343 more	Copy number loss	See cases	GPathogenic
Select item 153994	GRCh38/hg38 5q21.3-22.2(chr5:106586078-113006585)x1	EPB41L4A-DT, APC +134 more	Copy number loss	See cases	GPathogenic
Select item 153508	GRCh38/hg38 5q22.1(chr5:110469276-111738442)x1	CAMK4, LOC126807474 +32 more	Copy number loss	See cases	GUncertain significance
Select item 152734	GRCh38/hg38 5q14.3-23.1(chr5:92899734-119614119)x1	DMXL1, DMXL1-DT +496 more	Copy number loss	See cases	GPathogenic
Select item 151143	GRCh38/hg38 5q14.3-23.3(chr5:90374606-128076423)x1	LOC129994523, LOC129994524 +683 more	Copy number loss	See cases	GPathogenic
Select item 150860	GRCh38/hg38 5q14.3-22.1(chr5:84603580-111435081)x1	ADGRV1, ARB2A +436 more	Copy number loss	See cases	GPathogenic
Select item 150374	GRCh38/hg38 5q22.1-23.3(chr5:110687442-130103838)x1	LOC129389350, LOC129389351 +377 more	Copy number loss	See cases	GPathogenic
Select item 146399	GRCh38/hg38 5q21.3-23.1(chr5:107002209-118025316)x1	AP3S1, APC +230 more	Copy number loss	See cases	GPathogenic
Select item 144331	GRCh38/hg38 5q21.3-23.1(chr5:108585264-116815075)x1	AP3S1, APC +186 more	Copy number loss	See cases	GPathogenic
Select item 59672	GRCh38/hg38 5q21.3-33.2(chr5:106619588-156124387)x1	ABLIM3, ACSL6 +1672 more	Copy number loss	See cases	GPathogenic
Select item 59671	GRCh38/hg38 5q21.1-22.2(chr5:102373396-113594030)x1	EPB41L4A-DT, APC +180 more	Copy number loss	See cases	GPathogenic
Select item 59447	GRCh38/hg38 5q22.1(chr5:110564896-111731572)x3	CAMK4, LOC126807474 +31 more	Copy number gain	See cases	GUncertain significance
Select item 58098	GRCh38/hg38 5q15-22.3(chr5:96454445-114050905)x3	TSSK1B, WDR36 +275 more	Copy number gain	See cases	GPathogenic

ClinVar

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Germline classification

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Links from Gene

Items: 50