ClinVar for Gene (Select 55156) - ClinVar

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Links from Gene

Items: 38

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3129598	NM_018120.6(ARMC1):c.367G>A (p.Glu123Lys)	ARMC1 (E123K)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3129597	NM_018120.6(ARMC1):c.103G>A (p.Val35Ile)	ARMC1 (V35I)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 3063025	GRCh37/hg19 8p21.2-q21.3(chr8:27024288-89410121)x3	PREX2, PRKDC +240 more	Copy number gain	not specified	GPathogenic
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 2658630	NM_018120.6(ARMC1):c.12C>T (p.Ser4=)	ARMC1	Single nucleotide variant (5 prime UTR variant +1 more)	not provided	GLikely benign
Select item 2408739	NM_018120.6(ARMC1):c.47C>T (p.Ser16Leu)	ARMC1 (S16L)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2371095	NM_018120.6(ARMC1):c.133A>G (p.Ile45Val)	ARMC1 (I45V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2366585	NM_018120.6(ARMC1):c.464C>T (p.Thr155Met)	ARMC1 (T155M)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2344555	NM_018120.6(ARMC1):c.776G>A (p.Gly259Asp)	ARMC1 (G259D +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2332489	NM_018120.6(ARMC1):c.104T>G (p.Val35Gly)	ARMC1 (V35G)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2326280	NM_018120.6(ARMC1):c.379C>T (p.Arg127Cys)	ARMC1 (R127C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2248299	NM_018120.6(ARMC1):c.772G>C (p.Val258Leu)	ARMC1 (V156L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2222564	NM_018120.6(ARMC1):c.166G>A (p.Val56Ile)	ARMC1 (V56I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1809323	GRCh37/hg19 8q12.3-13.1(chr8:64049070-66671663)x1	ARMC1, BHLHE22 +4 more	Copy number loss	not provided	GUncertain significance
Select item 1703544	GRCh37/hg19 8p23.3-q24.3(chr8:158048-146295771)	AARD, ABRA +665 more	Copy number gain	Polydactyly	GPathogenic
Select item 1527436	GRCh37/hg19 8q12.3-13.2(chr8:65194424-68570319)	ADHFE1, ARFGEF1 +23 more	Copy number loss	not specified	GPathogenic
Select item 1340821	GRCh37/hg19 8q13.1-13.2(chr8:66045954-69807260)x1	ADHFE1, ARFGEF1 +23 more	Copy number loss	not provided	GPathogenic
Select item 687977	GRCh37/hg19 8q13.1(chr8:66320808-66641126)x3	ARMC1, MTFR1 +1 more	Copy number gain	not provided	GUncertain significance
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 686117	GRCh37/hg19 8q12.3-13.1(chr8:65280508-67782846)x1	ADHFE1, ARMC1 +14 more	Copy number loss	not provided	GPathogenic
Select item 563478	GRCh37/hg19 8q13.1(chr8:66403054-66705320)x3	MTFR1, PDE7A +1 more	Copy number gain	not provided	GUncertain significance
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 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 394884	GRCh37/hg19 8p23.3-q24.3(chr8:158991-146280828)x3	SCRT1, SCX +665 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 153737	GRCh38/hg38 8p21.3-q24.3(chr8:21291522-145070385)x3	LOC129999966, LOC129999967 +3111 more	Copy number gain	See cases	GPathogenic
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 150723	GRCh38/hg38 8q11.1-24.3(chr8:46031340-139285494)x3	LOC126860489, LOC126860490 +1963 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 145461	GRCh38/hg38 8q12.1-13.1(chr8:60519222-66659025)x3	ADHFE1, ARMC1 +150 more	Copy number gain	See cases	GPathogenic
Select item 144238	GRCh38/hg38 8q11.1-13.2(chr8:46031334-69303787)x3	ADHFE1, ALKAL1 +491 more	Copy number gain	See cases	GPathogenic
Select item 60364	GRCh38/hg38 8q12.3-21.11(chr8:62230636-73227786)x1	ADHFE1, ARFGEF1 +228 more	Copy number loss	See cases	GPathogenic
Select item 59788	GRCh38/hg38 8q12.3-21.13(chr8:61691800-82537696)x3	ADHFE1, ARFGEF1 +417 more	Copy number gain	See cases	GPathogenic
Select item 59787	GRCh38/hg38 8q12.1-21.13(chr8:57361243-79170078)x3	ADHFE1, ARFGEF1 +421 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

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Links from Gene

Items: 38