ClinVar for Gene (Select 81502) - ClinVar

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Links from Gene

Items: 41

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3062405	GRCh37/hg19 20q11.21(chr20:29917837-31886619)x3	BPIFB1, BPIFB2 +37 more	Copy number gain	not specified	GUncertain significance
Select item 2614997	NM_178581.3(HM13):c.436T>G (p.Ser146Ala)	HM13 (S146A)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2603355	NM_178581.3(HM13):c.1160G>A (p.Arg387His)	HM13, HM13-AS1 (R387H)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2512394	NM_178581.3(HM13):c.95T>C (p.Ile32Thr)	HM13 (I32T)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2461709	NM_178581.3(HM13):c.520G>A (p.Val174Ile)	HM13 (V174I)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2412208	NM_178581.3(HM13):c.32G>T (p.Gly11Val)	HM13 (G11V)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2390835	NM_178581.3(HM13):c.536G>A (p.Arg179Lys)	HM13 (R179K)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2377530	NM_178581.3(HM13):c.1163C>T (p.Pro388Leu)	HM13, HM13-AS1 (P388L)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2372421	NM_178581.3(HM13):c.1177G>A (p.Ala393Thr)	HM13, HM13-AS1 (A393T)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2370086	NM_178581.3(HM13):c.1120G>A (p.Asp374Asn)	HM13, HM13-AS1 (D374N)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2322700	NM_178581.3(HM13):c.439G>A (p.Gly147Arg)	HM13 (G147R)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2321931	NM_178581.3(HM13):c.73C>T (p.Pro25Ser)	HM13 (P25S)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2293787	NM_178581.3(HM13):c.121C>T (p.Leu41Phe)	HM13 (L41F)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2292884	NM_178581.3(HM13):c.41A>T (p.Glu14Val)	HM13 (E14V)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 1809278	GRCh37/hg19 20q11.21-11.23(chr20:29652122-35603726)x3	AAR2, ACSS2 +98 more	Copy number gain	not provided	GLikely pathogenic
Select item 1808687	GRCh37/hg19 20q11.21-11.23(chr20:29833535-34815537)x3	ACSS2, ACTL10 +86 more	Copy number gain	not provided	GLikely pathogenic
Select item 1526690	GRCh37/hg19 20p11.21-q11.22(chr20:25442597-33761550)	ACSS2, ACTL10 +71 more	Copy number gain	not specified	GPathogenic
Select item 1526688	GRCh37/hg19 20p11.21-q11.21(chr20:24162775-31820857)	ABHD12, ACSS1 +50 more	Copy number gain	not specified	GLikely pathogenic
Select item 1341087	GRCh37/hg19 20p11.23-q11.22(chr20:18665879-33903216)x3	ABHD12, ACSS1 +117 more	Copy number gain	not provided	GLikely pathogenic
Select item 1340492	GRCh37/hg19 20q11.21(chr20:29652122-30518304)x3	BCL2L1, COX4I2 +15 more	Copy number gain	not provided	GLikely benign
Select item 1340481	GRCh37/hg19 20q11.21(chr20:29833535-30195919)x3	DEFB115, DEFB116 +8 more	Copy number gain	not provided	GLikely benign
Select item 1340141	GRCh37/hg19 20q11.21(chr20:29652122-30272637)x3	BCL2L1, COX4I2 +10 more	Copy number gain	not provided	GLikely benign
Select item 979729	GRCh37/hg19 20q11.21(chr20:29833534-30494851)x3	DEFB115, DEFB123 +15 more	Copy number gain	not provided	GLikely benign
Select item 979562	GRCh37/hg19 20p11.23-q11.21(chr20:19750804-30479077)x3	CST9, ACSS1 +57 more	Copy number gain	not provided	GLikely pathogenic
Select item 816123	GRCh37/hg19 20q11.21(chr20:29651839-30195919)x3	REM1, DEFB116 +8 more	Copy number gain	not provided	GLikely benign
Select item 689044	GRCh37/hg19 20q11.21-11.23(chr20:29833608-35087952)x3	AAR2, ACSS2 +88 more	Copy number gain	not provided	GPathogenic
Select item 688778	GRCh37/hg19 20q11.21(chr20:29835457-30232565)x3	COX4I2, DEFB115 +9 more	Copy number gain	not provided	GUncertain significance
Select item 560101	Single allele	CST11, CST2 +89 more	Duplication	not provided	GPathogenic
Select item 446352	GRCh37/hg19 20q11.21(chr20:29425357-30226690)x3	COX4I2, DEFB115 +10 more	Copy number gain	See cases	GUncertain significance
Select item 443671	GRCh37/hg19 20p11.21-q11.21(chr20:24876569-30494851)x3	ABHD12, ACSS1 +27 more	Copy number gain	See cases	GUncertain significance
Select item 443340	GRCh37/hg19 20p13-q13.33(chr20:61569-62915555)x3	KIF3B, KIZ +540 more	Copy number gain	See cases	GPathogenic
Select item 443339	GRCh37/hg19 20p13-q13.33(chr20:61569-62915555)	AAR2, ABHD12 +540 more	Copy number gain	See cases	GPathogenic
Select item 442379	GRCh37/hg19 20q11.21(chr20:29833535-30599771)x3	BCL2L1, CCM2L +18 more	Copy number gain	See cases	GUncertain significance
Select item 395214	GRCh37/hg19 20q11.21(chr20:29877878-30231917)x3	COX4I2, DEFB116 +8 more	Copy number gain	See cases	GLikely benign
Select item 253408	GRCh37/hg19 20p12.1-q11.21(chr20:17705775-31600738)x3	CD93, PDRG1 +89 more	Copy number gain	See cases	GPathogenic
Select item 152494	GRCh38/hg38 20q11.21(chr20:31254983-31660401)x3	COX4I2, DEFB115 +27 more	Copy number gain	See cases	GUncertain significance
Select item 149125	GRCh38/hg38 20q11.21(chr20:31245583-32017285)x4	ABALON, BCL2L1 +62 more	Copy number gain	See cases	GLikely pathogenic
Select item 146596	GRCh38/hg38 20p13-q13.33(chr20:99557-64277321)x3	LOC130065566, LOC130065567 +2522 more	Copy number gain	See cases	GPathogenic
Select item 146032	GRCh38/hg38 20q11.21(chr20:31254983-33473080)x3	LOC121627902, LOC121853002 +160 more	Copy number gain	See cases	GPathogenic
Select item 145102	GRCh38/hg38 20q11.21(chr20:31254983-32575288)x3	ABALON, ASXL1 +104 more	Copy number gain	See cases	GPathogenic
Select item 59195	GRCh38/hg38 20p12.2-q12(chr20:9811433-39316956)x3	LOC130065574, LOC130065575 +950 more	Copy number gain	See cases	GPathogenic

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Links from Gene

Items: 41