ClinVar for Gene (Select 2919) - ClinVar

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Links from Gene

Items: 31

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3270398	NM_001511.4(CXCL1):c.296A>T (p.Lys99Met)	CXCL1 (K99M)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3270397	NM_001511.4(CXCL1):c.151G>A (p.Gly51Arg)	CXCL1 (G51R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3079165	NM_001511.4(CXCL1):c.184G>A (p.Val62Met)	CXCL1 (V62M)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3024631	GRCh37/hg19 4p12-q35.2(chr4:45455621-191003541)x3	HPGDS, SCRG1 +537 more	Copy number gain	not provided	GPathogenic
Select item 2685114	GRCh37/hg19 4q13.2-13.3(chr4:69146217-75500577)x1	ADAMTS3, AFM +58 more	Copy number loss	not provided	GPathogenic
Select item 2528374	NM_001511.4(CXCL1):c.130C>G (p.Gln44Glu)	CXCL1 (Q44E)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2397242	NM_001511.4(CXCL1):c.148C>A (p.Gln50Lys)	CXCL1 (Q50K)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2356554	NM_001511.4(CXCL1):c.183C>G (p.Asn61Lys)	CXCL1 (N61K)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2342161	NM_001511.4(CXCL1):c.170T>C (p.Ile57Thr)	CXCL1 (I57T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2308790	NM_001511.4(CXCL1):c.28C>T (p.Pro10Ser)	CXCL1 (P10S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 1684642	NC_000004.12:g.67833055_82716065del	BTC, CABS1 +330 more	Deletion	See cases	GPathogenic
Select item 1527095	GRCh37/hg19 4q13.3-21.21(chr4:73055313-80083154)	CXCL5, CXCL6 +51 more	Copy number loss	not specified	GPathogenic
Select item 1340288	GRCh37/hg19 4q12-31.21(chr4:52866944-143582507)x3	AASDH, ABCG2 +359 more	Copy number gain	not provided	GPathogenic
Select item 1098574	GRCh38/hg38 4q12-21.1(chr4:51891814-76009719)x1	ENAM, LOC123477761 +360 more	Copy number loss	Piebaldism	GPathogenic
Select item 983172	GRCh37/hg19 4q13.3-21.3(chr4:71412409-87920784)x1	ABRAXAS1, ADAMTS3 +97 more	Copy number loss	See cases	GPathogenic
Select item 814566	GRCh37/hg19 4q13.3-21.23(chr4:72680879-86426232)x1	CXCL3, LIN54 +82 more	Copy number loss	not provided	GPathogenic
Select item 814563	GRCh37/hg19 4q13.2-21.21(chr4:68950363-79738598)x1	ADAMTS3, AFM +92 more	Copy number loss	not provided	GPathogenic
Select item 784041	NM_001511.4(CXCL1):c.209C>T (p.Ala70Val)	CXCL1 (A70V)	Single nucleotide variant (missense variant +1 more)	not provided	GBenign
Select item 685523	GRCh37/hg19 4q13.3-21.1(chr4:71561780-78304341)x1	ADAMTS3, AFM +51 more	Copy number loss	not provided	GPathogenic
Select item 685236	GRCh37/hg19 4q13.2-21.22(chr4:68242784-82991431)x3	CCNG2, CCNI +109 more	Copy number gain	not provided	GPathogenic
Select item 562931	GRCh37/hg19 4q13.3(chr4:73952783-75261407)x3	CXCL1, EPGN +15 more	Copy number gain	not provided	GUncertain significance
Select item 443262	GRCh37/hg19 4q13.1-21.1(chr4:66017575-76772947)x1	ADAMTS3, AFM +75 more	Copy number loss	See cases	GPathogenic
Select item 441728	GRCh37/hg19 4p16.3-q35.2(chr4:68346-190957473)	AADAT, AASDH +745 more	Copy number gain	See cases	GPathogenic
Select item 441727	GRCh37/hg19 4p16.3-q35.2(chr4:68346-190957473)x3	MRPL1, MSANTD1 +745 more	Copy number gain	See cases	GPathogenic
Select item 394609	GRCh37/hg19 4p16.3-q35.2(chr4:12440-190904441)x3	H2AZ1, HADH +744 more	Copy number gain	See cases	GPathogenic
Select item 155391	GRCh38/hg38 4q13.2-22.3(chr4:68686088-95294456)x3	LOC129992695, LOC129992696 +533 more	Copy number gain	See cases	GPathogenic
Select item 149262	GRCh38/hg38 4q13.3-21.3(chr4:72262258-86002147)x3	ABRAXAS1, ADAMTS3 +331 more	Copy number gain	See cases	GPathogenic
Select item 148549	GRCh38/hg38 4q13.2-13.3(chr4:67799665-74240920)x1	ADAMTS3, AFM +121 more	Copy number loss	See cases	GLikely pathogenic
Select item 58031	GRCh38/hg38 4q13.3-21.21(chr4:71128874-78099088)x3	ADAMTS3, AFM +166 more	Copy number gain	See cases	GPathogenic
Select item 58029	GRCh38/hg38 4q12-22.3(chr4:51831622-97505618)x3	LOC129389216, LOC129389217 +757 more	Copy number gain	See cases	GPathogenic
Select item 57863	GRCh38/hg38 4q13.3(chr4:73510905-73978175)x3	CXCL1, CXCL6 +14 more	Copy number gain	See cases	GUncertain significance

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Links from Gene

Items: 31