Variant report

Variant	nsv64575
Chromosome Location	chr13:67401507-67403849
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 87 )
Associated
traits (count: 97 )

Variant overlapped rSNPs/rCNVs (count:87 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs74738197	chr13:67401507-67401508	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs528790219	chr13:67401520-67401521	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs9599157	chr13:67401531-67401532	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs569814368	chr13:67401562-67401563	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs201515088	chr13:67401580-67401581	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs565434592	chr13:67401597-67401598	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs530954342	chr13:67401608-67401609	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs577549603	chr13:67401658-67401659	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs544798639	chr13:67401693-67401694	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs550974694	chr13:67401713-67401714	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs147498736	chr13:67401725-67401726	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs148560726	chr13:67401743-67401744	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs367624447	chr13:67401763-67401764	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs558360849	chr13:67401776-67401777	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs115308786	chr13:67401797-67401798	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs565908179	chr13:67401799-67401800	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs534515268	chr13:67401879-67401880	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs192055557	chr13:67401909-67401910	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs184498270	chr13:67401917-67401918	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs142959758	chr13:67401922-67401923	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs114717163	chr13:67401959-67401960	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs116415708	chr13:67401965-67401966	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs542664805	chr13:67402037-67402038	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs552782268	chr13:67402082-67402083	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs35278079	chr13:67402108-67402109	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs199516252	chr13:67402115-67402116	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs573428436	chr13:67402122-67402123	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs74093623	chr13:67402160-67402161	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs565604173	chr13:67402183-67402184	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs150696697	chr13:67402220-67402221	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs544622475	chr13:67402237-67402238	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs554181092	chr13:67402273-67402274	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs563394147	chr13:67402353-67402354	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs367898602	chr13:67402407-67402408	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs189479273	chr13:67402433-67402434	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs77214075	chr13:67402491-67402492	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs547119545	chr13:67402492-67402493	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs530658126	chr13:67402506-67402507	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs140019996	chr13:67402556-67402557	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs181528763	chr13:67402564-67402565	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs80149754	chr13:67402569-67402570	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs149660405	chr13:67402617-67402618	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs146678430	chr13:67402674-67402675	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs556548218	chr13:67402700-67402701	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs11617188	chr13:67402728-67402729	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs575481196	chr13:67402840-67402841	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs553057553	chr13:67402933-67402934	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs71207607	chr13:67402942-67402943	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs369139479	chr13:67402943-67402944	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs199817881	chr13:67402957-67402958	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:97)

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
Myelofibrosis	22110671	CNVD

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:67401400-67405200	Weak transcription	Muscle Satellite Cultured Cells	--

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