ClinVar for Gene (Select 140738) - ClinVar

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Links from Gene

Items: 38

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3327082	NM_183240.3(TMEM37):c.205C>A (p.Gln69Lys)	TMEM37 (Q69K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3327081	NM_183240.3(TMEM37):c.88A>G (p.Ile30Val)	TMEM37 (I30V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3327080	NM_183240.3(TMEM37):c.451A>T (p.Asn151Tyr)	TMEM37 (N151Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3179442	NM_183240.3(TMEM37):c.461C>T (p.Thr154Ile)	TMEM37 (T154I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3179441	NM_183240.3(TMEM37):c.274C>T (p.Arg92Cys)	TMEM37 (R92C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3179440	NM_183240.3(TMEM37):c.125C>T (p.Ser42Leu)	TMEM37 (S42L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3062651	GRCh37/hg19 2q12.2-21.2(chr2:106755586-134302739)x1	ACOXL, ACTR3 +121 more	Copy number loss	not specified	GPathogenic
Select item 3062627	GRCh37/hg19 2q14.1-14.3(chr2:116646793-126388760)x1	C1QL2, C2orf76 +22 more	Copy number loss	not specified	GLikely pathogenic
Select item 2545932	NM_183240.3(TMEM37):c.52C>T (p.Arg18Cys)	TMEM37 (R18C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2520342	NM_183240.3(TMEM37):c.53G>A (p.Arg18His)	TMEM37 (R18H)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2463329	NM_183240.3(TMEM37):c.295G>A (p.Val99Met)	TMEM37 (V99M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2458418	NM_183240.3(TMEM37):c.301G>T (p.Ala101Ser)	TMEM37 (A101S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2369774	NM_183240.3(TMEM37):c.351C>A (p.Asp117Glu)	TMEM37 (D117E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2271101	NM_183240.3(TMEM37):c.61T>C (p.Phe21Leu)	TMEM37 (F21L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1809385	GRCh37/hg19 2q14.1-14.3(chr2:116761476-123897262)x1	C1QL2, C2orf76 +21 more	Copy number loss	not provided	GPathogenic
Select item 1808512	GRCh37/hg19 2q14.2(chr2:120079538-120626557)x4	C2orf76, DBI +4 more	Copy number gain	not provided	GUncertain significance
Select item 1703543	GRCh37/hg19 2p25.3-q37.3(chr2:1-243199373)	ABCA12, ABCB11 +1216 more	Copy number gain	Mosaic trisomy 2	GPathogenic
Select item 1679114	GRCh37/hg19 2q13-22.3(chr2:112475655-145691999)x3	EPB41L5, ERCC3 +120 more	Copy number gain	2q13q22.3 microduplication syndrome	GPathogenic
Select item 1526888	GRCh37/hg19 2q13-14.3(chr2:113188197-128144700)	ACTR3, BIN1 +51 more	Copy number loss	not specified	GPathogenic
Select item 1341178	GRCh37/hg19 2q14.2(chr2:119967365-121555029)x3	C2orf76, DBI +10 more	Copy number gain	not provided	GUncertain significance
Select item 1340017	GRCh37/hg19 2q13-22.3(chr2:111484468-146333604)x3	GPR39, IL1F10 +122 more	Copy number gain	not provided	GPathogenic
Select item 814298	GRCh37/hg19 2q14.2-14.3(chr2:118903294-123099547)x1	TMEM177, TFCP2L1 +18 more	Copy number loss	not provided	GPathogenic
Select item 814297	GRCh37/hg19 2q14.2-14.3(chr2:118872395-128069813)x1	BIN1, PTPN4 +24 more	Copy number loss	not provided	GPathogenic
Select item 814296	GRCh37/hg19 2q14.1-14.2(chr2:115416190-122399064)x1	TMEM177, C2orf76 +20 more	Copy number loss	not provided	GPathogenic
Select item 780835	NM_183240.3(TMEM37):c.230G>A (p.Gly77Asp)	TMEM37 (G77D)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 767819	NM_183240.3(TMEM37):c.208_209insGTGTGC (p.Thr70delinsSerValPro)	TMEM37	Insertion (inframe_indel)	not provided	GBenign
Select item 562675	GRCh37/hg19 2q14.1-14.3(chr2:114707932-124328692)x1	STEAP3, PTPN4 +23 more	Copy number loss	not provided	GPathogenic
Select item 562561	GRCh37/hg19 2q14.2(chr2:120003938-120280012)x3	DBI, TMEM37 +3 more	Copy number gain	not provided	GLikely benign
Select item 524189	Single allele	ACMSD, C2orf27A +486 more	Deletion	not provided	GLikely pathogenic
Select item 523163	GRCh37/hg19 2q12.1-24.3(chr2:104172062-168223828)x1	CCDC74B, CCDC93 +218 more	Copy number loss	Poly (ADP-Ribose) polymerase inhibitor response	Gdrug response
Select item 442998	GRCh37/hg19 2p25.3-q37.3(chr2:12771-242783384)	RGPD4, RGPD5 +1214 more	Copy number gain	See cases	GPathogenic
Select item 442997	GRCh37/hg19 2p25.3-q37.3(chr2:12771-242783384)x3	IL1F10, IL1R1 +1214 more	Copy number gain	See cases	GPathogenic
Select item 442443	GRCh37/hg19 2q14.1-14.3(chr2:116754600-123897370)x1	C1QL2, C2orf76 +21 more	Copy number loss	See cases	GPathogenic
Select item 442204	GRCh37/hg19 2q13-14.3(chr2:114056441-123673800)x1	FOXD4L1, ACTR3 +27 more	Copy number loss	See cases	GPathogenic
Select item 253388	GRCh37/hg19 2q12.3-14.3(chr2:109798247-125658380)x1	RGPD8, ACTR3 +63 more	Copy number loss	See cases	GPathogenic
Select item 155658	GRCh38/hg38 2q14.2-14.3(chr2:118687829-121621814)x1	C1QL2, C2orf76 +92 more	Copy number loss	See cases	GPathogenic
Select item 153085	GRCh38/hg38 2q14.1-14.3(chr2:115302067-129071130)x1	AMMECR1L, BIN1 +254 more	Copy number loss	See cases	GPathogenic
Select item 60184	GRCh38/hg38 2q14.1-21.3(chr2:118086324-134964738)x1	ACMSD, AMER3 +391 more	Copy number loss	See cases	GPathogenic

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Links from Gene

Items: 38