Variant report

Variant	nsv961073
Chromosome Location	chr18:14785627-14792591
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 354 )
Associated
traits (count: 56 )

Variant overlapped rSNPs/rCNVs (count:354 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs573357146	chr18:14785691-14785692	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs151013319	chr18:14785705-14785706	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs562253830	chr18:14785803-14785804	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs191602890	chr18:14785808-14785809	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs562910986	chr18:14785872-14785873	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs183740052	chr18:14785874-14785875	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs551833542	chr18:14785893-14785894	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs367833401	chr18:14785894-14785895	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs559545148	chr18:14785905-14785906	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs528262433	chr18:14785910-14785911	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs548322712	chr18:14785917-14785918	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs568265363	chr18:14785931-14785932	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs537322497	chr18:14785960-14785961	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs141079576	chr18:14786005-14786006	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs551031622	chr18:14786031-14786032	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs10572502	chr18:14786044-14786045	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs398032057	chr18:14786070-14786071	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs188803908	chr18:14786118-14786119	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs570839196	chr18:14786147-14786148	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs149679291	chr18:14786148-14786149	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs181172835	chr18:14786191-14786192	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs147792345	chr18:14786192-14786193	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs141265325	chr18:14786296-14786297	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs555902828	chr18:14786304-14786305	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs575865181	chr18:14786306-14786307	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs544487631	chr18:14786308-14786309	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs562972086	chr18:14786315-14786316	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs186388594	chr18:14786345-14786346	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs545533437	chr18:14786380-14786381	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs528204561	chr18:14786418-14786419	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs527514803	chr18:14786422-14786423	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs548104362	chr18:14786424-14786425	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs561884844	chr18:14786470-14786471	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs113726659	chr18:14786524-14786525	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs376376199	chr18:14786551-14786552	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs570901927	chr18:14786558-14786559	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs539854354	chr18:14786590-14786591	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs138455504	chr18:14786618-14786619	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs190060045	chr18:14786629-14786630	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs535911152	chr18:14786685-14786686	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs74986665	chr18:14786699-14786700	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs12605171	chr18:14786742-14786743	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs555719021	chr18:14786773-14786774	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs149193935	chr18:14786807-14786808	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs560399218	chr18:14786818-14786819	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs558019598	chr18:14786882-14786883	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs577873090	chr18:14786905-14786906	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs181641470	chr18:14786916-14786917	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs559272339	chr18:14786951-14786952	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs546260638	chr18:14786971-14786972	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:56)

Disease	PMID	Source
Chronic lymphocytic leukemia	21546498	CNVD
Intellectual disability	22102821	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Acute myeloid leukemia	16864856	CNVD
Seminomas	18059402	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Kartagener syndrome	16639409	CNVD
Basal cell lymphoma	21115979	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Cancer	21183584	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Basal cell lymphoma	17053054	CNVD
Colorectal cancer	19359472	CNVD
Human rectal carcinomas	16397240	CNVD
Melanoma	18172304	CNVD
Colorectal cancer	16272173	CNVD
Colorectal cancer	19150955	CNVD
Follicular lymphoma	20505157	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	18923191	CNVD
Glioblastoma multiforme	21080181	CNVD
Cancer	21637783	CNVD
Medulloblastoma	21979893	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Trisomy 18 syndrome	17576883	CNVD
lymphocytic leukemia	21291569	CNVD
Barrett''s syndrome	19417022	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Ewing''s sarcoma	17952124	CNVD
Multiple myeloma	17550852	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Breast cancer	21364760	CNVD
Heart disease	21282601	CNVD
Glioblastoma multiforme	21922591	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Acute myeloid leukemia	17377590	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Lung cancer	18438408	CNVD
Breast cancer	16620391	CNVD
Myelofibrosis	22110671	CNVD
Retinoblastoma	21504564	CNVD
Glioma	17123091	CNVD
Neurodevelopmental disorder	22521361	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
small cell lung cancer	20016488	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:14779400-14796600	Weak transcription	Osteobl	bone

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