Variant report

Variant	nsv981949
Chromosome Location	chr8:69437326-69438055
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 36 )
Associated
traits (count: 100 )

Variant overlapped rSNPs/rCNVs (count:36 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs141237240	chr8:69437360-69437361	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs376781969	chr8:69437385-69437386	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs528392472	chr8:69437388-69437389	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs548187014	chr8:69437398-69437399	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs568090405	chr8:69437514-69437515	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs184458358	chr8:69437523-69437524	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs536305075	chr8:69437591-69437592	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs190542810	chr8:69437642-69437643	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs146970852	chr8:69437644-69437645	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs546682317	chr8:69437649-69437650	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs539102975	chr8:69437653-69437654	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs114182675	chr8:69437658-69437659	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs573353271	chr8:69437663-69437664	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs566308784	chr8:69437678-69437679	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs555768101	chr8:69437679-69437680	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs542267643	chr8:69437706-69437707	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs182207314	chr8:69437718-69437719	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs544640577	chr8:69437723-69437724	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs185950541	chr8:69437730-69437731	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs533474826	chr8:69437787-69437788	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs190822442	chr8:69437790-69437791	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs111932097	chr8:69437792-69437793	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs528266634	chr8:69437793-69437794	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs138044435	chr8:69437847-69437848	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs185691654	chr8:69437858-69437859	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs190416952	chr8:69437873-69437874	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs546014614	chr8:69437878-69437879	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs550168006	chr8:69437975-69437976	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs10110831	chr8:69437994-69437995	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs539193870	chr8:69438016-69438017	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs200337190	chr8:69438017-69438018	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs142192026	chr8:69438018-69438019	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs201342464	chr8:69438022-69438023	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs397815502	chr8:69438023-69438024	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs117039781	chr8:69438025-69438026	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs369626810	chr8:69438035-69438036	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:100)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Gastric cancer	17908304	CNVD
Melanoma	18172304	CNVD
Medulloblastoma	21979893	CNVD
Ewing''s sarcoma	21437220	CNVD
Autism	19415332	CNVD
Malaria	21533027	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Esophageal cancer	21851588	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21245420	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Seminomas	18059402	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Pancreatic cancer	21811587	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	21080181	CNVD
Breast cancer	17603634	CNVD
Testicular cancer	18059402	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21509527	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Cancer	20164919	CNVD
primary effusion lymphomas	17116491	CNVD
Esophageal cancer	20955586	CNVD
Multiple myeloma	16461302	CNVD
abnormal development	18461090	CNVD
Cancer	20164920	CNVD
Oral cancer	21386901	CNVD
Uveal melanoma	21693616	CNVD
Langer-Giedion syndrome	22283845	CNVD
Cancer	21637783	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	20632083	CNVD
Breast cancer	19602461	CNVD
Cancer	22429812	CNVD
Endometrial cancer	22040021	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Oral cancer	19627613	CNVD
Prostate cancer	21088497	CNVD
colon cancer	17210682	CNVD
Breast cancer	21264507	CNVD
Breast cancer	22028636	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	16751803	CNVD
Salivary gland tumor	18059337	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Gastric cancer	17167181	CNVD
Colorectal cancer	19359472	CNVD
Breast cancer	16461572	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	16968546	CNVD
head and neck squamous cell carcinoma	18028549	CNVD
Breast cancer	17001317	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ewing''s sarcoma	17952124	CNVD
Urothelial carcinoma	21177765	CNVD
Lung cancer	18438408	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	16608533	CNVD
Metanephric adenoma	20802469	CNVD
Hepatocellular carcinoma	18803288	CNVD
Prostate cancer	18632612	CNVD
Glioblastoma multiforme	18628472	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	16573809	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Colorectal cancer	16272173	CNVD
Melanoma	22183965	CNVD
Cancer	21949371	CNVD
Non-small cell lung cancer	21829676	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Acute myeloid leukemia	21358987	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Adenocarcinoma	21044232	CNVD
Squamous cell cancer	20885788	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Sezary syndrome	18413736	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
head and neck squamous cell carcinoma	16715129	CNVD
Prostate cancer	16461572	CNVD
Ovarian cancer	20844748	CNVD
Breast cancer	21399628	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	22522925	CNVD
Colorectal cancer	21645411	CNVD

Chromatin state (count:1 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:69423800-69445600	Weak transcription	Aorta	Aorta

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links