Variant report

Variant	nsv9084
Chromosome Location	chr13:67011210-67014947
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 140 )
Associated
traits (count: 96 )

Variant overlapped rSNPs/rCNVs (count:140 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs113165030	chr13:67011337-67011338	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs531692953	chr13:67011355-67011356	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs186420050	chr13:67011376-67011377	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs143133398	chr13:67011395-67011396	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs560238751	chr13:67011408-67011409	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs201037429	chr13:67011412-67011413	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs112829507	chr13:67011439-67011440	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs538474973	chr13:67011442-67011443	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs552401453	chr13:67011447-67011448	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs539071574	chr13:67011470-67011471	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs377157456	chr13:67011471-67011472	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs569788324	chr13:67011478-67011479	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs142759667	chr13:67011479-67011480	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs549219419	chr13:67011485-67011486	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs150620197	chr13:67011513-67011514	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs66796123	chr13:67011537-67011538	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs398023161	chr13:67011558-67011559	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs139725160	chr13:67011687-67011688	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs533870240	chr13:67011715-67011716	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs553602598	chr13:67011739-67011740	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs373579559	chr13:67011760-67011761	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs531371269	chr13:67011780-67011781	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs577341858	chr13:67011856-67011857	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs546085400	chr13:67011863-67011864	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs563136421	chr13:67011881-67011882	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs34154192	chr13:67011887-67011888	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs576802467	chr13:67011911-67011912	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs542594054	chr13:67011941-67011942	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs549675550	chr13:67011959-67011960	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs189611640	chr13:67012020-67012021	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs143703161	chr13:67012024-67012025	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs375670656	chr13:67012042-67012043	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs564424864	chr13:67012054-67012055	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs146828652	chr13:67012091-67012092	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs115988267	chr13:67012093-67012094	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs140664076	chr13:67012108-67012109	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs537726558	chr13:67012129-67012130	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs573568208	chr13:67012136-67012137	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs181536765	chr13:67012149-67012150	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs533575612	chr13:67012167-67012168	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs186861634	chr13:67012239-67012240	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs576877314	chr13:67012250-67012251	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs529335781	chr13:67012272-67012273	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs556795558	chr13:67012290-67012291	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs642827	chr13:67012293-67012294	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs565826820	chr13:67012325-67012326	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs547465940	chr13:67012346-67012347	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs542503668	chr13:67012361-67012362	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs573919913	chr13:67012366-67012367	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs517198	chr13:67012381-67012382	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:96)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
HIV/AIDS	22032296	CNVD
Prostate cancer	16705090	CNVD
High-proliferative meningiomas	17937814	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Autism	22495311	CNVD
Chordoma	21602918	CNVD
Bladder cancer	21949216	CNVD
Acute myeloid leukemia	16864856	CNVD
Burkitt''s lymphoma	18698080	CNVD
Cancer	21637783	CNVD
Medulloblastoma	21979893	CNVD
Chronic lymphocytic leukemia	21518781	CNVD
colon cancer	17210682	CNVD
Endometrial cancer	22040021	CNVD
Colorectal cancer	20709793	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Ovarian cancer	20844748	CNVD
Colorectal cancer	19359472	CNVD
Intracranial aneurysm	19064780	CNVD
Breast cancer	19287154	CNVD
Acute myeloid leukemia	18379011	CNVD
Human rectal carcinomas	16397240	CNVD
Olfactory neuroblastoma	18408657	CNVD
Multiple myeloma	17077331	CNVD
Ependymoma	16718352	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Colorectal cancer	16272173	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Squamous cell cancer	20885788	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Thyroid cancer	19087340	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Breast cancer	16608533	CNVD
Neuroblastoma	18923191	CNVD
Ovarian cancer	22174824	CNVD
Breast cancer	17133270	CNVD
Myoepithelioma	18604193	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Prostate cancer	16573809	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Paraganglioma	21461997	CNVD
Pheochromocytoma	21461997	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Prostate cancer	17245344	CNVD
Prostate cancer	18632612	CNVD
Colorectal cancer	21586687	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Retinoblastoma	19183342	CNVD
Developmental delay	21147756	CNVD
Melanoma	18172304	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Merkel cell carcinoma	19020549	CNVD
Basal cell lymphoma	17053054	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
lymphocytic leukemia	21291569	CNVD
Breast cancer	21858162	CNVD
Glioblastoma multiforme	21922591	CNVD
Metanephric adenoma	20802469	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Gastric cancer	17908304	CNVD
Glioblastoma multiforme	21750150	CNVD
Breast cancer	17603634	CNVD
Cancer	21183584	CNVD
Breast cancer	17393978	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Liposarcoma	21253554	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Colorectal cancer	16774939	CNVD
Adenoid cystic carcinoma	17372589	CNVD
abnormal development	18461090	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute myeloid leukemia	20729466	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Prostate cancer	16461572	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
Schizophrenia	23813976	CNVD
Prostate cancer	22341455	CNVD

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:67005400-67016400	Weak transcription	Brain Substantia Nigra	brain

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