Variant report

Variant	nsv960155
Chromosome Location	chr17:15765431-15766496
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 43 )
Associated
traits (count: 125 )

Variant overlapped rSNPs/rCNVs (count:43 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs144361853	chr17:15765445-15765446	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs146701016	chr17:15765475-15765476	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs538630032	chr17:15765480-15765481	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs514780	chr17:15765481-15765482	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs558915002	chr17:15765517-15765518	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs371019172	chr17:15765524-15765525	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs373024433	chr17:15765526-15765527	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs28604277	chr17:15765530-15765531	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs56256939	chr17:15765531-15765532	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs577821476	chr17:15765535-15765536	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs513190	chr17:15765591-15765592	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs58711104	chr17:15765608-15765609	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs513076	chr17:15765627-15765628	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs137909713	chr17:15765630-15765631	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs573861557	chr17:15765660-15765661	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs71358373	chr17:15765719-15765720	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs542855866	chr17:15765776-15765777	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs140659663	chr17:15765791-15765792	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs531436917	chr17:15765799-15765800	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs661571	chr17:15765817-15765818	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs58259296	chr17:15765839-15765840	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs569892450	chr17:15765856-15765857	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs564886906	chr17:15765884-15765885	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs527341867	chr17:15765925-15765926	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs113643975	chr17:15765935-15765936	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs547662937	chr17:15766011-15766012	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs538750409	chr17:15766067-15766068	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs509405	chr17:15766070-15766071	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs487494	chr17:15766099-15766100	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs530198539	chr17:15766100-15766101	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs72302868	chr17:15766121-15766122	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs549984636	chr17:15766168-15766169	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs397832294	chr17:15766180-15766181	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs397832290	chr17:15766190-15766191	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs570007152	chr17:15766231-15766232	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs539134878	chr17:15766251-15766252	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs535390481	chr17:15766272-15766273	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs566064289	chr17:15766349-15766350	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs113268267	chr17:15766367-15766368	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs149303667	chr17:15766388-15766389	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs554095330	chr17:15766407-15766408	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs574002419	chr17:15766422-15766423	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs571928792	chr17:15766490-15766491	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:125)

Disease	PMID	Source
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	17603634	CNVD
Melanoma	18172304	CNVD
Glioblastoma multiforme	19435819	CNVD
Non-small cell lung cancer	19010865	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Colorectal cancer	16774939	CNVD
Hepatocellular carcinoma	18803288	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Burkitt''s lymphoma	19759907	CNVD
Wilms tumour	21544195	CNVD
Esophageal adenocarcinoma	18519675	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Medulloblastoma	21979893	CNVD
Breast cancer	16608533	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Chordoma	21602918	CNVD
Miller-Dieker syndrome	22283845	CNVD
Non-syndromic sensorineural hearing loss	17457615	CNVD
Cancer	22429812	CNVD
Chronic lymphocytic leukemia	21795749	CNVD
Ewing''s sarcoma	21437220	CNVD
Follicular lymphoma	19010834	CNVD
Colorectal cancer	20709793	CNVD
Acute myeloid leukemia	16864856	CNVD
Endometrial cancer	22040021	CNVD
Paraganglioma	21461997	CNVD
Pheochromocytoma	21461997	CNVD
Breast cancer	22028636	CNVD
Breast cancer	20837533	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
colon cancer	17210682	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Basal cell lymphoma	17053054	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Cancer	16751803	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Colorectal cancer	19359472	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Chronic lymphocytic leukemia	17971485	CNVD
Basal cell lymphoma	17170743	CNVD
Breast cancer	16461572	CNVD
Colorectal cancer	16272173	CNVD
Follicular lymphoma	17170743	CNVD
Human rectal carcinomas	16397240	CNVD
Breast cancer	17133270	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Ovarian cancer	22174824	CNVD
Moyamoya disease	22323933	CNVD
small cell lung cancer	20016488	CNVD
Acute myeloid leukemia	20729466	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Urothelial carcinoma	21177765	CNVD
Acute myeloid leukemia	21251322	CNVD
Myelodysplastic syndrome	21251322	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Acute myeloid leukemia	20724749	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Acute myeloid leukemia	17237825	CNVD
Colorectal cancer	21645411	CNVD
HIV/AIDS	22844521	CNVD
Psoriasis	22844521	CNVD
Rheumatoid arthritis	22844521	CNVD
Sclerosis systemic	22844521	CNVD
Systemic lupus erythematosus	22844521	CNVD
HIV/AIDS	17953491	CNVD
HIV/AIDS	20877625	CNVD
Immune disease	21076436	CNVD
Rheumatoid arthritis	17953491	CNVD
Type 1 diabetes	17953491	CNVD
HIV/AIDS	15637236	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Ovarian cancer	21781307	CNVD
Autism	22495311	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Neurofibromatosis	18196300	CNVD
Adenoid cystic carcinoma	18332873	CNVD
Multiple myeloma	16616336	CNVD
Multiple myeloma	17550852	CNVD
Pancreatic cancer	21811587	CNVD
Autism	17322880	CNVD
Hereditary neuropathy with liability to pressure palsy	19521722	CNVD
Schizophrenia	19571808	CNVD
Schizophrenia	19955444	CNVD
Charcot-marie-tooth disease	18787571	CNVD
Breast cancer	20409316	CNVD
Autism	18414403	CNVD
Breast cancer	17001317	CNVD
Rhabdomyosarcoma	16790082	CNVD
Myelofibrosis	22110671	CNVD
Peripheral neuropathy	21193943	CNVD
Schizophrenia	20587603	CNVD
Schizophrenia	22958593	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Ovarian cancer	20844748	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Charcot-marie-tooth disease	16463004	CNVD
Osteosarcoma	22292074	CNVD
Charcot	16760730	CNVD
Mental retardation	17901693	CNVD
ovarian endometriomas	16273235	CNVD
Breast cancer	21858162	CNVD
Ovarian cancer	21720365	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	17142309	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Autism	22102821	CNVD
Gastric cancer	18160780	CNVD

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:15765400-15773800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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