Variant report

Variant	nsv973630
Chromosome Location	chr9:44088181-44090734
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 121 )
Associated
traits (count: 68 )

Variant overlapped rSNPs/rCNVs (count:121 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs577510922	chr9:44088194-44088195	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs368963028	chr9:44088346-44088347	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs552982036	chr9:44088390-44088391	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs375135400	chr9:44088391-44088392	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs371331032	chr9:44088420-44088421	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs374463785	chr9:44088428-44088429	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs541941241	chr9:44088437-44088438	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs554308717	chr9:44088458-44088459	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs575841534	chr9:44088467-44088468	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs543654663	chr9:44088487-44088488	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs565025434	chr9:44088489-44088490	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs62538271	chr9:44088502-44088503	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs367750944	chr9:44088565-44088566	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs532473123	chr9:44088614-44088615	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs202154264	chr9:44088640-44088641	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs374955160	chr9:44088756-44088757	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs540648708	chr9:44088795-44088796	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs559413544	chr9:44088811-44088812	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs529782886	chr9:44088812-44088813	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs550778499	chr9:44088843-44088844	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs548318243	chr9:44088850-44088851	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs190320826	chr9:44088870-44088871	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs531010323	chr9:44088885-44088886	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs552775786	chr9:44088898-44088899	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs62538273	chr9:44088899-44088900	Weak transcription	n/a	n/a	Overlapped CNVs	mRNA abundance
26	rs553007244	chr9:44088929-44088930	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs552918642	chr9:44088988-44088989	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs568130553	chr9:44089027-44089028	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs112602125	chr9:44089186-44089187	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs573150398	chr9:44089217-44089218	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs192837559	chr9:44089247-44089248	Weak transcription	n/a	n/a	Overlapped CNVs	mRNA abundance
32	rs557037881	chr9:44089334-44089335	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs575738238	chr9:44089347-44089348	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs185729007	chr9:44089362-44089363	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs558745260	chr9:44089369-44089370	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs62538274	chr9:44089391-44089392	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs541336921	chr9:44089394-44089395	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs190201649	chr9:44089401-44089402	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs575320003	chr9:44089405-44089406	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs544329776	chr9:44089412-44089413	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs541895134	chr9:44089544-44089545	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs563361952	chr9:44089565-44089566	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs370176434	chr9:44089598-44089599	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs564311761	chr9:44089629-44089630	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs577832194	chr9:44089667-44089668	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs571044330	chr9:44089671-44089672	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs528745486	chr9:44089673-44089674	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs546898557	chr9:44089684-44089685	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs181017956	chr9:44089741-44089742	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs535453612	chr9:44089767-44089768	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:68)

Disease	PMID	Source
Gastric cancer	21586687	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Myopathy	18421352	CNVD
Neuroblastoma	18664255	CNVD
Acute lymphoblastic leukemia	18957548	CNVD
Myeloproliferative neoplasm	17564968	CNVD
Malignant meningioma	17937814	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Glioma	21971842	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Melanoma	18172304	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	17603634	CNVD
Medulloblastoma	21979893	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Glioblastoma multiforme	21080181	CNVD
Hepatocellular carcinoma	22174799	CNVD
Oligodendroglial tumors	17285580	CNVD
Cutaneous squamous cell carcinomas	19131950	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17133270	CNVD
Chordoma	18071362	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chordoma	21602918	CNVD
Renal cell carcinoma	18592004	CNVD
Developmental delay	19490664	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
microdeletion syndrome	16199537	CNVD
Cancer	20164919	CNVD
Ovarian cancer	21720365	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Urothelial carcinoma	21177765	CNVD
Renal cell carcinoma	21668985	CNVD
Autism	22495311	CNVD
Melanoma	22183965	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Cancer	16751803	CNVD
Myelofibrosis	22110671	CNVD
lymphocytic leukemia	21291569	CNVD
Non-syndromic sensorineural hearing loss	17289997	CNVD
Oral cancer	21386901	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21509527	CNVD
Sezary syndrome	18413736	CNVD
early-passage human iPS cells	21368824	CNVD
Schizophrenia	21346763	CNVD
Breast cancer	21990379	CNVD
Astrocytoma	22246337	CNVD
Lung adenocarcinoma	17086460	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Lung cancer	17086460	CNVD
Rhabdomyosarcoma	16790082	CNVD
Schizophrenia	20967226	CNVD
Schizophrenia	23813976	CNVD
Breast cancer	22522925	CNVD

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:44071000-44092000	Weak transcription	Liver	Liver

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