il1b[All Fields] AND 1[has_clinical] - dbVar - NCBI

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Number of Variants: 17

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv3910630	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr2: 50,739,936-242,751,149 , GRCh37.p13 chr2: 50,886,432-243,102,476 , GRCh38.p12 chr2: 50,659,294-242,160,331	IL1B, DAZAP2P1, 2991 more genes
nsv3873957	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 109,798,247-125,658,380 , GRCh38.p12 chr2: 109,181,791-124,900,803	IL1B, MTND1P28, 230 more genes
nsv6313770	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 113,188,197-128,144,700 , GRCh38.p12 chr2: 112,430,620-127,387,124	IL1B, LOC105373575, 174 more genes
nsv3872550	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 106,423,310-115,054,828 , GRCh38.p12 chr2: 105,806,853-114,297,251	IL1B, SMIM12P1, 189 more genes
nsv3888610	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 109,556,627-117,570,152 , GRCh38.p12 chr2: 108,940,171-116,812,576	IL1B, LOC112268438, 149 more genes
nsv6315390	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 1-243,199,373 , GRCh38.p12 chr2: 10,001-242,157,305	IL1B, LOC112268439, 3737 more genes
nsv3874648	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 15,672-243,101,834 , GRCh38.p12 chr2: 15,672-242,157,305	IL1B, IGKV2OR2-10, 3737 more genes
nsv3885544	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 14,238-243,048,760 , GRCh38.p12 chr2: 14,238-242,106,609	IL1B, RNU6-674P, 3735 more genes
nsv3882615	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr2: 12,771-242,783,384 , GRCh38.p12 chr2: 12,771-241,841,232	IL1B, MTND2P22, 3724 more genes
nsv6291353	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 111,484,468-146,333,604 , GRCh38.p12 chr2: 110,726,891-145,576,036	IL1B, LINC01120, 490 more genes
nsv6314748	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 112,475,655-145,691,999 , GRCh38.p12 chr2: 111,718,078-144,934,432	IL1B, MED15P9, 474 more genes
nsv3876227	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 96,353,030-114,045,463 , GRCh38.p12 chr2: 95,687,282-113,287,886	IL1B, RNU4-8P, 346 more genes
nsv3921207	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr2: 110,857,227-116,449,787 , GRCh37.p13 chr2: 111,334,455-116,733,317 , GRCh38.p12 chr2: 110,576,878-115,975,741	IL1B, RABL2A, 98 more genes
nsv6314726	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr2: 40,607,042-146,902,764 , GRCh38.p12 chr2: 40,379,902-146,145,196	IL1B, ACTG2, 1713 more genes
nsv3923963	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr2: 110,190,938-242,751,149 , GRCh37.p13 chr2: 110,833,649-243,102,476 , GRCh38.p12 chr2: 110,076,072-242,160,331	IL1B, NMTRQ-TTG9-1, 1944 more genes
nsv3876086	copy number variation	1	nstd102	human	drug response	GRCh37 chr2: 104,172,062-168,223,828 , GRCh38.p12 chr2: 103,555,604-167,367,318	IL1B, SLC4A10, 871 more genes
nsv6291237	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr2: 113,295,194-114,085,649 , GRCh38.p12 chr2: 112,537,617-113,328,072	IL1B, CKAP2L, 30 more genes

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il1b[All Fields] AND 1[has_clinical] (18)
dbVar
Burns
Burns
Injuries to tissues caused by contact with heat, steam, chemicals (BURNS, CHEMICAL), electricity (BURNS, ELECTRIC), or the like.<br/>

MeSH
D002056 (1)
MeSH

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