Nexn Variant Search Result - Rat Genome Database

Advanced Search (OLGA)

Variants search result for Homo sapiens
(View Results for all Objects and Ontologies)

795 records found for search term Nexn

Refine Term:

Assembly:

Chr

Sort By:

Export

CSV

TAB

RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
8555557	CV15364	deletion	NEXN, 3-BP DEL, 1948GGA	Dilated cardiomyopathy 1CC [RCV000000353]	pathogenic				Human		name
155747749	CV1849751	single nucleotide variant	NM_144573.4(NEXN):c.-1C>T	Cardiovascular phenotype [RCV002417129]	uncertain significance	1	77916106	77916106	Human		name
8692250	CV142216	single nucleotide variant	NM_144573.4(NEXN):c.-58T>C	not specified [RCV000127195]	benign	1	77888754	77888754	Human		name
9691017	CV172456	single nucleotide variant	NM_144573.4(NEXN):c.-10T>C	not specified [RCV000156717]	uncertain significance	1	77916097	77916097	Human		name
10055883	CV198073	single nucleotide variant	NM_144573.4(NEXN):c.-34C>A	not specified [RCV000183641]	benign	1	77916073	77916073	Human		name
11593930	CV281843	single nucleotide variant	NM_144573.4(NEXN):c.*22C>G	not provided [RCV001636402]	benign\|likely benign	1	77942851	77942851	Human		name
13538750	CV498791	single nucleotide variant	NM_144573.4(NEXN):c.-43T>A	not specified [RCV000612285]	likely benign	1	77916064	77916064	Human		name
150407459	CV1192908	single nucleotide variant	NM_144573.4(NEXN):c.28-9C>T	Dilated cardiomyopathy 1CC [RCV005225439]\|not provided [RCV001572349]	likely benign	1	77917557	77917557	Human	1	name
152173416	CV1662601	single nucleotide variant	NM_144573.4(NEXN):c.27+7C>T	Dilated cardiomyopathy 1CC [RCV002144097]	likely benign	1	77916140	77916140	Human	1	name
11651404	CV281219	single nucleotide variant	NM_144573.3(NEXN):c.-233T>C	Dilated Cardiomyopathy, Dominant [RCV000298645]\|Hypertrophic cardiomyopathy [RCV000341829]	uncertain significance	1	77888579	77888579	Human	1	name
11652721	CV281220	single nucleotide variant	NM_144573.3(NEXN):c.-194A>G	Dilated Cardiomyopathy, Dominant [RCV000306583]\|Hypertrophic cardiomyopathy [RCV000363525]	uncertain significance	1	77888618	77888618	Human	1	name
11583160	CV281231	single nucleotide variant	NM_144573.4(NEXN):c.*279G>A	not provided [RCV001577177]	likely benign\|uncertain significance	1	77943108	77943108	Human		name
11583998	CV281232	single nucleotide variant	NM_144573.4(NEXN):c.*314A>C	not provided [RCV001568183]	likely benign\|uncertain significance	1	77943143	77943143	Human		name
11585031	CV281236	single nucleotide variant	NM_144573.4(NEXN):c.*414A>C	not provided [RCV003406569]	benign\|uncertain significance	1	77943243	77943243	Human		name
11652332	CV281242	duplication	NM_144573.3(NEXN):c.*511dup	Dilated Cardiomyopathy, Dominant [RCV000363598]\|Hypertrophic cardiomyopathy [RCV000304217]	likely benign	1	77943338	77943339	Human	1	name
11647438	CV281841	single nucleotide variant	NM_144573.3(NEXN):c.-128A>G	Dilated Cardiomyopathy, Dominant [RCV000276219]\|Hypertrophic cardiomyopathy [RCV000333658]	uncertain significance	1	77888684	77888684	Human	1	name
11591075	CV281845	single nucleotide variant	NM_144573.3(NEXN):c.*356A>G	Dilated Cardiomyopathy, Dominant [RCV000384521]\|Hypertrophic cardiomyopathy [RCV000325328]	uncertain significance	1	77943185	77943185	Human	1	name
11584103	CV281850	single nucleotide variant	NM_144573.3(NEXN):c.*362G>C	Dilated Cardiomyopathy, Dominant [RCV000271326]\|Hypertrophic cardiomyopathy [RCV000331120]	uncertain significance	1	77943191	77943191	Human	1	name
11658709	CV281853	deletion	NM_144573.4(NEXN):c.*418del	Dilated Cardiomyopathy, Dominant [RCV000373077]\|Dilated cardiomyopathy 1CC [RCV002487322]\|Hypertrophic cardiomyopathy [RCV000351117]	uncertain significance	1	77943238	77943238	Human	4	name
11650978	CV281856	duplication	NM_144573.4(NEXN):c.*418dup	Dilated Cardiomyopathy, Dominant [RCV000296079]\|Hypertrophic cardiomyopathy [RCV000385787]	likely benign	1	77943237	77943238	Human	3	name
11646859	CV281861	single nucleotide variant	NM_144573.3(NEXN):c.*661A>G	Dilated Cardiomyopathy, Dominant [RCV000272972]\|Hypertrophic cardiomyopathy [RCV000309311]	uncertain significance	1	77943490	77943490	Human	1	name
11582641	CV281868	single nucleotide variant	NM_144573.3(NEXN):c.*809T>G	Dilated Cardiomyopathy, Dominant [RCV000261163]\|Hypertrophic cardiomyopathy [RCV000316334]	uncertain significance	1	77943638	77943638	Human	1	name
11651979	CV283083	single nucleotide variant	NM_144573.3(NEXN):c.-230A>C	Dilated Cardiomyopathy, Dominant [RCV000302271]\|Hypertrophic cardiomyopathy [RCV000394778]	uncertain significance	1	77888582	77888582	Human	1	name
11588050	CV283084	single nucleotide variant	NM_144573.3(NEXN):c.*209A>G	Dilated Cardiomyopathy, Dominant [RCV000300049]\|Hypertrophic cardiomyopathy [RCV000359470]	uncertain significance	1	77943038	77943038	Human	1	name
11657207	CV283092	single nucleotide variant	NM_144573.3(NEXN):c.*418A>C	Dilated Cardiomyopathy, Dominant [RCV000339344]\|Hypertrophic cardiomyopathy [RCV000393274]	uncertain significance	1	77943247	77943247	Human	1	name
11591913	CV283112	single nucleotide variant	NM_144573.3(NEXN):c.*759T>A	Dilated Cardiomyopathy, Dominant [RCV000333692]\|Hypertrophic cardiomyopathy [RCV000388248]	uncertain significance	1	77943588	77943588	Human	1	name
11651459	CV283301	microsatellite	NM_144573.4(NEXN):c.*4CT[1]	Cardiomyopathy [RCV000768812]\|Dilated Cardiomyopathy, Dominant [RCV000402554]\|Hypertrophic cardiomyopathy [RCV000298933]\|not provided [RCV001618514]\|not specified [RCV004701400]	benign\|likely benign\|uncertain significance	1	77942833	77942834	Human		name
11648363	CV283313	single nucleotide variant	NM_144573.3(NEXN):c.*899G>A	Dilated Cardiomyopathy, Dominant [RCV000281375]\|Hypertrophic cardiomyopathy [RCV000375851]	uncertain significance	1	77943728	77943728	Human	1	name
150467580	CV1277594	deletion	NM_144573.4(NEXN):c.28-85del	not provided [RCV001710889]	benign	1	77917476	77917476	Human		name
151715550	CV1392734	single nucleotide variant	NM_144573.4(NEXN):c.688-1G>C	Cardiovascular phenotype [RCV004651799]\|Dilated cardiomyopathy 1CC [RCV001908895]	conflicting interpretations of pathogenicity\|uncertain significance	1	77926715	77926715	Human	2	name
151740154	CV1412874	single nucleotide variant	NM_144573.4(NEXN):c.219+5T>G	Dilated cardiomyopathy 1CC [RCV001926388]	uncertain significance	1	77917762	77917762	Human	1	name
9692065	CV172458	single nucleotide variant	NM_144573.4(NEXN):c.447+5C>T	Cardiovascular phenotype [RCV002326867]\|not specified [RCV000151559]	uncertain significance	1	77918278	77918278	Human		name
9691202	CV172459	single nucleotide variant	NM_144573.4(NEXN):c.865-5G>A	Cardiovascular phenotype [RCV002444647]\|Dilated cardiomyopathy 1CC [RCV001456331]\|Primary dilated cardiomyopathy [RCV000157392]\|not provided [RCV000869575]\|not specified [RCV000156912]	likely benign\|conflicting interpretations of pathogenicity\|uncertain significance	1	77929311	77929311	Human	3	name
155977615	CV1886167	single nucleotide variant	NM_144573.4(NEXN):c.688-1G>A	Dilated cardiomyopathy 1CC [RCV003075494]	likely pathogenic	1	77926715	77926715	Human	1	name
156411834	CV1972750	single nucleotide variant	NM_144573.4(NEXN):c.298+9C>T	Dilated cardiomyopathy 1CC [RCV002587619]	likely benign	1	77918047	77918047	Human	1	name
156117072	CV2035630	single nucleotide variant	NM_144573.4(NEXN):c.687+6T>A	Dilated cardiomyopathy 1CC [RCV002785635]	uncertain significance	1	77926617	77926617	Human	1	name
156152815	CV2098543	single nucleotide variant	NM_144573.4(NEXN):c.28-12C>A	Dilated cardiomyopathy 1CC [RCV002890711]	likely benign	1	77917554	77917554	Human	1	name
11345958	CV238346	single nucleotide variant	NM_144573.4(NEXN):c.687+4A>T	Cardiomyopathy [RCV001798744]\|Cardiovascular phenotype [RCV002365219]\|Dilated cardiomyopathy 1CC [RCV000226888]\|not provided [RCV001697593]\|not specified [RCV005418030]	uncertain significance	1	77926615	77926615	Human	4	name
401887017	CV2784431	single nucleotide variant	NM_144573.4(NEXN):c.865-1G>A	Cardiovascular phenotype [RCV003387407]	uncertain significance	1	77929315	77929315	Human		name
11592646	CV281243	single nucleotide variant	NM_144573.3(NEXN):c.*1020T>A	Dilated Cardiomyopathy, Dominant [RCV000340936]\|Hypertrophic cardiomyopathy [RCV000376965]	uncertain significance	1	77943849	77943849	Human	1	name
405075819	CV3100281	single nucleotide variant	NM_144573.4(NEXN):c.298+2T>C	Dilated cardiomyopathy 1CC [RCV003799834]	likely pathogenic	1	77918040	77918040	Human	1	name
597880732	CV3868381	deletion	NM_144573.4(NEXN):c.220-7del	Dilated cardiomyopathy 1CC [RCV005217281]	likely benign	1	77917952	77917952	Human	1	name
597838424	CV3871053	single nucleotide variant	NM_144573.4(NEXN):c.687+2T>C	Dilated cardiomyopathy 1CC [RCV005210713]	likely pathogenic	1	77926613	77926613	Human	1	name
13540026	CV498600	deletion	NM_144573.4(NEXN):c.-52-4del	not provided [RCV001712707]	likely benign	1	77916045	77916045	Human		name
13535877	CV498613	single nucleotide variant	NM_144573.4(NEXN):c.220-6A>G	Dilated cardiomyopathy 1CC [RCV005209518]\|not specified [RCV000608182]	likely benign	1	77917954	77917954	Human	1	name
8610770	CV57068	single nucleotide variant	NM_144573.4(NEXN):c.299-3T>C	Cardiomyopathy [RCV001798221]\|Dilated cardiomyopathy 1CC [RCV002513573]\|not specified [RCV000041175]	uncertain significance	1	77918122	77918122	Human	3	name
14688769	CV615194	single nucleotide variant	NM_144573.4(NEXN):c.865-4T>C	Cardiomyopathy [RCV000769819]\|Cardiovascular phenotype [RCV002442574]	uncertain significance	1	77929312	77929312	Human	2	name
15115263	CV685109	single nucleotide variant	NM_144573.4(NEXN):c.865-9T>C	Dilated cardiomyopathy 1CC [RCV000860699]\|not provided [RCV001561270]	likely benign	1	77929307	77929307	Human	1	name
126772953	CV1003009	single nucleotide variant	NM_144573.4(NEXN):c.1659+5C>T	Dilated cardiomyopathy 1CC [RCV001324047]	uncertain significance	1	77942213	77942213	Human	1	name
127266705	CV1089326	single nucleotide variant	NM_144573.4(NEXN):c.448-10C>T	Dilated cardiomyopathy 1CC [RCV001440312]	likely benign	1	77925178	77925178	Human	1	name
150334557	CV1164099	single nucleotide variant	NM_144573.4(NEXN):c.865-17A>G	Dilated cardiomyopathy 1CC [RCV002070371]\|not provided [RCV001529710]\|not specified [RCV001699811]	benign\|likely benign	1	77929299	77929299	Human	1	name
150424716	CV1182964	single nucleotide variant	NM_144573.4(NEXN):c.-53+36T>G	not provided [RCV001557028]	likely benign	1	77888795	77888795	Human		name
150425023	CV1182965	single nucleotide variant	NM_144573.4(NEXN):c.864+43T>G	not provided [RCV001557452]	likely benign	1	77926935	77926935	Human		name
150465273	CV1201049	deletion	NM_144573.4(NEXN):c.448-47del	not provided [RCV001587529]	likely benign	1	77925137	77925137	Human		name
151232920	CV1320020	single nucleotide variant	NM_144573.4(NEXN):c.1473+5A>G	Cardiomyopathy [RCV001799376]	uncertain significance	1	77936049	77936049	Human	2	name
151723499	CV1494625	deletion	NM_144573.4(NEXN):c.1251+1del	Dilated cardiomyopathy 1CC [RCV001983393]\|not provided [RCV002223331]	likely pathogenic\|uncertain significance	1	77933479	77933479	Human	1	name
152981663	CV1676972	single nucleotide variant	NM_144573.4(NEXN):c.1252-1G>A	Dilated cardiomyopathy 1CC [RCV003093990]\|not specified [RCV002248039]	likely pathogenic\|uncertain significance	1	77935822	77935822	Human	1	name
153346143	CV1691579	single nucleotide variant	NM_144573.4(NEXN):c.1251+1G>A	Cardiomyopathy [RCV002273062]	uncertain significance	1	77933480	77933480	Human	2	name
155950174	CV1879108	single nucleotide variant	NM_144573.4(NEXN):c.220-17T>C	Dilated cardiomyopathy 1CC [RCV003074101]	likely benign	1	77917943	77917943	Human	1	name
156349096	CV1889653	single nucleotide variant	NM_144573.4(NEXN):c.864+11A>G	Dilated cardiomyopathy 1CC [RCV003090822]	likely benign	1	77926903	77926903	Human	1	name
10049900	CV191105	deletion	NM_144573.4(NEXN):c.1252-5del	not provided [RCV000174177]	uncertain significance	1	77935811	77935811	Human		name
10055882	CV198072	single nucleotide variant	NM_144573.4(NEXN):c.-52-16T>C	not specified [RCV000183640]	benign	1	77916039	77916039	Human		name
10055884	CV198081	deletion	NM_144573.4(NEXN):c.687+23del	Cardiomyopathy [RCV000183642]\|Dilated cardiomyopathy 1CC [RCV002054183]\|not specified [RCV001699149]	benign	1	77926631	77926631	Human	3	name
156244463	CV1991630	single nucleotide variant	NM_144573.4(NEXN):c.447+11A>T	Dilated cardiomyopathy 1CC [RCV002645688]	likely benign	1	77918284	77918284	Human	1	name
156017648	CV2019152	single nucleotide variant	NM_144573.4(NEXN):c.490-14A>G	Dilated cardiomyopathy 1CC [RCV002690844]	likely benign	1	77926400	77926400	Human	1	name
156207974	CV2103150	single nucleotide variant	NM_144573.4(NEXN):c.1659+2T>C	Dilated cardiomyopathy 1CC [RCV002918048]	uncertain significance	1	77942210	77942210	Human	1	name
156212010	CV2175766	single nucleotide variant	NM_144573.4(NEXN):c.1659+8G>A	Dilated cardiomyopathy 1CC [RCV003024841]	likely benign	1	77942216	77942216	Human	1	name
156232379	CV2184159	single nucleotide variant	NM_144573.4(NEXN):c.490-15T>A	Dilated cardiomyopathy 1CC [RCV003043135]	likely benign	1	77926399	77926399	Human	1	name
11349238	CV238347	single nucleotide variant	NM_144573.4(NEXN):c.688-10G>A	Dilated cardiomyopathy 1CC [RCV001493385]\|NEXN-related disorder [RCV004532969]\|not provided [RCV000229736]\|not specified [RCV000605590]	likely benign	1	77926706	77926706	Human	2	name , trait , alternate_id
404981315	CV3099739	single nucleotide variant	NM_144573.4(NEXN):c.1659+9C>T	Dilated cardiomyopathy 1CC [RCV003791568]	likely benign	1	77942217	77942217	Human	1	name
405087018	CV3107990	duplication	NM_144573.4(NEXN):c.1473+7dup	Dilated cardiomyopathy 1CC [RCV003800688]	likely benign	1	77936049	77936050	Human	1	name
12848153	CV365510	single nucleotide variant	NM_144573.4(NEXN):c.299-14T>C	Dilated cardiomyopathy 1CC [RCV002059839]\|not specified [RCV000444767]	likely benign	1	77918111	77918111	Human	1	name
597884359	CV3866321	single nucleotide variant	NM_144573.4(NEXN):c.1473+8A>G	Dilated cardiomyopathy 1CC [RCV005217797]	likely benign	1	77936052	77936052	Human	1	name
597909714	CV3870829	single nucleotide variant	NM_144573.4(NEXN):c.490-16C>T	Dilated cardiomyopathy 1CC [RCV005221691]	likely benign	1	77926398	77926398	Human	1	name
597877290	CV3871567	single nucleotide variant	NM_144573.4(NEXN):c.688-11C>T	Dilated cardiomyopathy 1CC [RCV005216783]	likely benign	1	77926705	77926705	Human	1	name
597841393	CV3873718	single nucleotide variant	NM_144573.4(NEXN):c.865-19G>A	Dilated cardiomyopathy 1CC [RCV005226545]	likely benign	1	77929297	77929297	Human	1	name
597851951	CV3877151	single nucleotide variant	NM_144573.4(NEXN):c.865-12T>G	Dilated cardiomyopathy 1CC [RCV005228380]	likely benign	1	77929304	77929304	Human	1	name
597857762	CV3877860	single nucleotide variant	NM_144573.4(NEXN):c.489+19T>C	Dilated cardiomyopathy 1CC [RCV005229169]	likely benign	1	77925248	77925248	Human	1	name
616936934	CV4010877	single nucleotide variant	NM_144573.4(NEXN):c.1474-7C>G	not specified [RCV005404224]	likely benign	1	77942016	77942016	Human		name
13620086	CV516113	single nucleotide variant	NM_144573.4(NEXN):c.299-10A>G	Dilated cardiomyopathy 1CC [RCV000647291]	likely benign	1	77918115	77918115	Human	1	name
8610752	CV57050	single nucleotide variant	NM_144573.4(NEXN):c.1053+1G>A	Cardiomyopathy [RCV001798218]\|Cardiovascular phenotype [RCV004018905]\|Dilated cardiomyopathy 1CC [RCV000692171]\|Hypertrophic cardiomyopathy 20 [RCV002466420]\|NEXN-related disorder [RCV004537144]\|Primary familial hypertrophic cardiomyopathy [RCV000208507]\|not pro ... (more) vided [RCV000766515]\|not specified [RCV000041156]	conflicting interpretations of pathogenicity\|uncertain significance	1	77929505	77929505	Human	6	name , trait , alternate_id
8610768	CV57066	single nucleotide variant	NM_144573.4(NEXN):c.298+10T>C	not specified [RCV000041173]	likely benign	1	77918048	77918048	Human		name
8610769	CV57067	deletion	NM_144573.4(NEXN):c.299-14del	not provided [RCV001668169]\|not specified [RCV000041174]	benign\|likely benign	1	77918104	77918104	Human		name
8610779	CV57077	single nucleotide variant	NM_144573.4(NEXN):c.864+12T>A	Dilated cardiomyopathy 1CC [RCV002054805]\|NEXN-related disorder [RCV004537145]\|not provided [RCV001529294]\|not specified [RCV000041185]	benign\|likely benign\|conflicting interpretations of pathogenicity\|uncertain significance	1	77926904	77926904	Human	2	name , trait , alternate_id
14728427	CV657923	single nucleotide variant	NM_144573.4(NEXN):c.27+200T>C	not provided [RCV000834769]	benign	1	77916333	77916333	Human		name
14725936	CV658066	single nucleotide variant	NM_144573.4(NEXN):c.27+220A>C	not provided [RCV000833654]	benign	1	77916353	77916353	Human		name
14718328	CV658068	single nucleotide variant	NM_144573.4(NEXN):c.219+25G>A	not provided [RCV000830358]	benign	1	77917782	77917782	Human		name
14710059	CV658093	duplication	NM_144573.4(NEXN):c.1252-5dup	Cardiovascular phenotype [RCV002409004]\|Dilated cardiomyopathy 1CC [RCV003768597]\|not provided [RCV000841497]	benign\|likely benign	1	77935810	77935811	Human	2	name
15105693	CV774545	single nucleotide variant	NM_144573.4(NEXN):c.1252-6T>C	Dilated cardiomyopathy 1CC [RCV001431025]	likely benign	1	77935817	77935817	Human	1	name
26923602	CV850812	single nucleotide variant	NM_144573.4(NEXN):c.1473+1G>T	Dilated cardiomyopathy 1CC [RCV001064288]	uncertain significance	1	77936045	77936045	Human	1	name
150502773	CV1223302	single nucleotide variant	NM_144573.4(NEXN):c.489+106T>C	not provided [RCV001621236]	benign	1	77925335	77925335	Human		name
150492582	CV1225502	single nucleotide variant	NM_144573.4(NEXN):c.-53+141G>T	not provided [RCV001619018]	benign	1	77888900	77888900	Human	3	name
150450277	CV1232660	single nucleotide variant	NM_144573.4(NEXN):c.489+207C>T	not provided [RCV001647735]	benign	1	77925436	77925436	Human		name
150449745	CV1254017	deletion	NM_144573.4(NEXN):c.1660-80del	not provided [RCV001667654]	benign	1	77942371	77942371	Human		name
8692249	CV142215	single nucleotide variant	NM_144573.4(NEXN):c.1659+18C>G	Dilated cardiomyopathy 1CC [RCV002055714]\|not provided [RCV001529933]\|not specified [RCV000127194]	benign\|likely benign	1	77942226	77942226	Human	1	name
152126471	CV1596248	single nucleotide variant	NM_144573.4(NEXN):c.1252-12T>A	Dilated cardiomyopathy 1CC [RCV002118522]	likely benign	1	77935811	77935811	Human	1	name
152171961	CV1598911	single nucleotide variant	NM_144573.4(NEXN):c.1251+10T>C	Dilated cardiomyopathy 1CC [RCV002143613]	likely benign	1	77933489	77933489	Human	1	name
9690006	CV172462	single nucleotide variant	NM_144573.4(NEXN):c.1252-10T>G	Cardiomyopathy [RCV003149948]\|Dilated cardiomyopathy 1CC [RCV000862187]\|NEXN-related disorder [RCV004544441]\|not provided [RCV001704131]\|not specified [RCV000155650]	benign\|likely benign\|conflicting interpretations of pathogenicity\|uncertain significance	1	77935813	77935813	Human	4	name , trait , alternate_id
10055917	CV198107	deletion	NM_144573.3(NEXN):c.2026_*1del	Cardiovascular phenotype [RCV002415786]\|Dilated cardiomyopathy 1CC [RCV001043340]\|not provided [RCV001704887]\|not specified [RCV000183688]	uncertain significance	1	77942824	77942827	Human	2	name
156313998	CV2017843	single nucleotide variant	NM_144573.4(NEXN):c.1474-18T>C	Dilated cardiomyopathy 1CC [RCV002671792]	likely benign	1	77942005	77942005	Human	1	name
401775569	CV2724142	deletion	NM_144573.4(NEXN):c.25_27+2del	Cardiovascular phenotype [RCV003305662]	uncertain significance	1	77916130	77916134	Human		name
405087030	CV3107991	deletion	NM_144573.4(NEXN):c.1473+15del	Dilated cardiomyopathy 1CC [RCV003800689]	likely benign	1	77936059	77936059	Human	1	name
405074148	CV3111550	single nucleotide variant	NM_144573.4(NEXN):c.1660-16A>C	Dilated cardiomyopathy 1CC [RCV003809890]	likely benign	1	77942445	77942445	Human	1	name
12843155	CV365394	single nucleotide variant	NM_144573.4(NEXN):c.1252-16T>C	not specified [RCV000435721]	likely benign	1	77935807	77935807	Human		name
12848122	CV365409	single nucleotide variant	NM_144573.4(NEXN):c.1473+15T>C	not provided [RCV001698155]	likely benign	1	77936059	77936059	Human		name
12836340	CV365420	single nucleotide variant	NM_144573.4(NEXN):c.1474-10T>C	Dilated cardiomyopathy 1CC [RCV001454603]\|not provided [RCV001703866]	likely benign	1	77942013	77942013	Human	1	name
597885241	CV3866466	single nucleotide variant	NM_144573.4(NEXN):c.1252-14A>C	Dilated cardiomyopathy 1CC [RCV005217942]	likely benign	1	77935809	77935809	Human	1	name
597839693	CV3867755	single nucleotide variant	NM_144573.4(NEXN):c.1251+13G>T	Dilated cardiomyopathy 1CC [RCV005210951]	likely benign	1	77933492	77933492	Human	1	name
13520981	CV495342	single nucleotide variant	NM_144573.4(NEXN):c.1252-11T>G	Dilated cardiomyopathy 1CC [RCV002062113]\|not provided [RCV000599078]	likely benign\|uncertain significance	1	77935812	77935812	Human	1	name
13539343	CV498602	single nucleotide variant	NM_144573.4(NEXN):c.1252-13A>C	not specified [RCV000613151]	likely benign	1	77935810	77935810	Human		name
13530930	CV498847	single nucleotide variant	NM_144573.4(NEXN):c.1252-20C>A	Dilated cardiomyopathy 1CC [RCV002066640]\|not specified [RCV000606305]	likely benign	1	77935803	77935803	Human	1	name
14718330	CV657924	single nucleotide variant	NM_144573.4(NEXN):c.1251+43C>G	not provided [RCV000830359]	benign	1	77933522	77933522	Human		name
14719188	CV657983	single nucleotide variant	NM_144573.4(NEXN):c.447+105A>G	not provided [RCV000830666]	likely benign	1	77918378	77918378	Human		name
14736063	CV658076	single nucleotide variant	NM_144573.4(NEXN):c.864+231A>G	not provided [RCV000838298]	likely benign	1	77927123	77927123	Human		name
14745875	CV658080	single nucleotide variant	NM_144573.4(NEXN):c.864+290C>T	not provided [RCV000843841]	benign	1	77927182	77927182	Human		name
14714797	CV658084	single nucleotide variant	NM_144573.4(NEXN):c.864+294A>G	not provided [RCV000829157]	benign	1	77927186	77927186	Human		name
14718973	CV658091	single nucleotide variant	NM_144573.4(NEXN):c.1251+48T>C	not provided [RCV000830570]	benign	1	77933527	77933527	Human		name
150423485	CV1182966	single nucleotide variant	NM_144573.4(NEXN):c.1054-206G>A	not provided [RCV001555384]	likely benign	1	77933076	77933076	Human		name
150439751	CV1201592	single nucleotide variant	NM_144573.4(NEXN):c.1252-241T>C	not provided [RCV001583404]	likely benign	1	77935582	77935582	Human		name
150482427	CV1244275	duplication	NM_144573.4(NEXN):c.1474-198dup	not provided [RCV001653122]	benign	1	77941824	77941825	Human		name
14745890	CV657986	single nucleotide variant	NM_144573.4(NEXN):c.1252-301T>C	not provided [RCV000843856]	benign	1	77935522	77935522	Human		name
14729775	CV658086	single nucleotide variant	NM_144573.4(NEXN):c.1053+128T>C	not provided [RCV000835373]	benign	1	77929632	77929632	Human		name
404987218	CV3083707	deletion	NM_144573.4(NEXN):c.865-9_892del	Dilated cardiomyopathy 1CC [RCV003782060]	likely pathogenic	1	77929306	77929342	Human	1	name
12900630	CV405241	microsatellite	NM_144573.4(NEXN):c.687+8TTTG[2]	Dilated cardiomyopathy 1CC [RCV005208570]\|not specified [RCV000482817]	benign\|likely benign\|uncertain significance	1	77926619	77926622	Human		name
11588468	CV283312	insertion	NM_144573.3(NEXN):c.417_418insC	Dilated Cardiomyopathy, Dominant [RCV000404266]\|Hypertrophic cardiomyopathy [RCV000303151]	likely benign	1	77943246	77943247	Human	1	name
155686537	CV1852621	single nucleotide variant	NM_144573.4(NEXN):c.27G>A (p.Glu9=)	Cardiovascular phenotype [RCV002441560]	uncertain significance	1	77916133	77916133	Human		name
11646845	CV283295	microsatellite	NM_144573.3(NEXN):c.-212_-210GGC[7]	Dilated Cardiomyopathy, Dominant [RCV000272577]\|Hypertrophic cardiomyopathy [RCV000364861]\|not provided [RCV004691225]	uncertain significance	1	77888598	77888599	Human		name
404991783	CV3091336	single nucleotide variant	NM_144573.4(NEXN):c.15C>T (p.Ser5=)	Dilated cardiomyopathy 1CC [RCV003792809]	likely benign	1	77916121	77916121	Human	1	name
152052649	CV1607271	deletion	NM_144573.4(NEXN):c.220-19_220-16del	Dilated cardiomyopathy 1CC [RCV002109169]	likely benign	1	77917938	77917941	Human	1	name
152158072	CV1639560	microsatellite	NM_144573.4(NEXN):c.220-13_220-10del	Dilated cardiomyopathy 1CC [RCV002180429]	likely benign	1	77917942	77917945	Human		name
152090605	CV1654876	deletion	NM_144573.4(NEXN):c.490-21_490-18del	Dilated cardiomyopathy 1CC [RCV002212670]	likely benign	1	77926391	77926394	Human	1	name
155738754	CV1801457	single nucleotide variant	NM_144573.4(NEXN):c.45T>C (p.Ser15=)	Cardiovascular phenotype [RCV002342380]	likely benign	1	77917583	77917583	Human		name
155700322	CV1821057	single nucleotide variant	NM_144573.4(NEXN):c.8A>T (p.Asp3Val)	Cardiovascular phenotype [RCV002376339]\|NEXN-related disorder [RCV004534076]	uncertain significance	1	77916114	77916114	Human	1	name , trait , alternate_id
597698216	CV3565791	single nucleotide variant	NM_144573.4(NEXN):c.54C>A (p.Val18=)	Cardiovascular phenotype [RCV004987534]	likely benign	1	77917592	77917592	Human		name
597698220	CV3565792	single nucleotide variant	NM_144573.4(NEXN):c.69A>G (p.Val23=)	Cardiovascular phenotype [RCV004987535]	likely benign	1	77917607	77917607	Human		name
13476002	CV448242	single nucleotide variant	NM_144573.4(NEXN):c.78T>C (p.Leu26=)	Cardiomyopathy [RCV001170494]\|Cardiovascular phenotype [RCV000617787]\|Dilated cardiomyopathy 1CC [RCV000526535]\|not provided [RCV001696999]\|not specified [RCV000615643]	benign\|likely benign	1	77917616	77917616	Human	4	name
13527140	CV509225	single nucleotide variant	NM_144573.4(NEXN):c.1A>C (p.Met1Leu)	Cardiovascular phenotype [RCV000619501]\|Dilated cardiomyopathy 1CC [RCV002531762]	uncertain significance	1	77916107	77916107	Human	2	name
15197076	CV762083	single nucleotide variant	NM_144573.4(NEXN):c.66T>C (p.Tyr22=)	Cardiovascular phenotype [RCV002363402]\|Dilated cardiomyopathy 1CC [RCV000934404]\|not provided [RCV001529774]\|not specified [RCV001699472]	benign\|likely benign	1	77917604	77917604	Human	2	name
127272549	CV1067593	single nucleotide variant	NM_144573.4(NEXN):c.133A>C (p.Arg45=)	Dilated cardiomyopathy 1CC [RCV001405743]	likely benign	1	77917671	77917671	Human	1	name
127255422	CV1089325	single nucleotide variant	NM_144573.4(NEXN):c.270A>G (p.Val90=)	Cardiovascular phenotype [RCV002438995]\|Dilated cardiomyopathy 1CC [RCV001426561]	likely benign	1	77918010	77918010	Human	2	name
127302828	CV1131720	single nucleotide variant	NM_144573.4(NEXN):c.207G>A (p.Arg69=)	Dilated cardiomyopathy 1CC [RCV001499183]	likely benign	1	77917745	77917745	Human	1	name
150419268	CV1196667	single nucleotide variant	NM_144573.4(NEXN):c.135A>G (p.Arg45=)	not provided [RCV001577097]	likely benign	1	77917673	77917673	Human		name
152135935	CV1560503	single nucleotide variant	NM_144573.4(NEXN):c.195A>G (p.Arg65=)	Dilated cardiomyopathy 1CC [RCV002137541]	likely benign	1	77917733	77917733	Human	1	name
9690062	CV172457	single nucleotide variant	NM_144573.4(NEXN):c.237T>C (p.Ala79=)	Cardiovascular phenotype [RCV000248876]\|Dilated cardiomyopathy 1CC [RCV001436210]\|not specified [RCV000155711]	likely benign	1	77917977	77917977	Human	2	name
9689313	CV172596	single nucleotide variant	NM_144573.4(NEXN):c.249G>A (p.Glu83=)	Cardiomyopathy [RCV000768798]\|Cardiovascular phenotype [RCV002426746]\|Dilated cardiomyopathy 1CC [RCV001086673]\|NEXN-related disorder [RCV004544414]\|not provided [RCV000724770]\|not specified [RCV000154797]	likely benign\|conflicting interpretations of pathogenicity\|uncertain significance	1	77917989	77917989	Human	4	name , trait , alternate_id
9692067	CV173020	deletion	NM_144573.4(NEXN):c.1660-11_1660-7del	Dilated cardiomyopathy 1CC [RCV002514918]\|not specified [RCV000151561]	likely benign\|uncertain significance	1	77942446	77942450	Human	1	name
155696043	CV1840923	single nucleotide variant	NM_144573.4(NEXN):c.108A>G (p.Glu36=)	Cardiovascular phenotype [RCV002443818]	likely benign	1	77917646	77917646	Human		name
11096490	CV228514	single nucleotide variant	NM_144573.4(NEXN):c.156C>T (p.Asp52=)	Cardiomyopathy [RCV001170495]\|Cardiovascular phenotype [RCV000622079]\|Dilated cardiomyopathy 1CC [RCV000465499]\|not provided [RCV001726046]\|not specified [RCV000223646]	benign\|likely benign	1	77917694	77917694	Human	4	name
11346588	CV238345	single nucleotide variant	NM_144573.4(NEXN):c.222T>C (p.Ile74=)	Cardiovascular phenotype [RCV002429136]\|Dilated cardiomyopathy 1CC [RCV000229049]\|not specified [RCV005404426]	likely benign	1	77917962	77917962	Human	2	name
401777352	CV2730293	single nucleotide variant	NM_144573.4(NEXN):c.246T>C (p.Asp82=)	Cardiovascular phenotype [RCV003306352]	likely benign	1	77917986	77917986	Human		name
405269923	CV3187542	single nucleotide variant	NM_144573.4(NEXN):c.151A>C (p.Arg51=)	not provided [RCV003887626]	uncertain significance	1	77917689	77917689	Human		name
405727898	CV3391084	single nucleotide variant	NM_144573.4(NEXN):c.138T>C (p.Asn46=)	Cardiovascular phenotype [RCV004524745]	likely benign	1	77917676	77917676	Human		name
597698225	CV3565793	single nucleotide variant	NM_144573.4(NEXN):c.123C>A (p.Ala41=)	Cardiovascular phenotype [RCV004987536]	likely benign	1	77917661	77917661	Human		name
597698230	CV3565794	single nucleotide variant	NM_144573.4(NEXN):c.162A>G (p.Lys54=)	Cardiovascular phenotype [RCV004987537]	likely benign	1	77917700	77917700	Human		name
13534042	CV509227	single nucleotide variant	NM_144573.4(NEXN):c.141A>G (p.Gln47=)	Cardiovascular phenotype [RCV000618228]	likely benign	1	77917679	77917679	Human		name
14688359	CV614728	single nucleotide variant	NM_144573.4(NEXN):c.216G>A (p.Gln72=)	Cardiomyopathy [RCV000768797]	likely benign	1	77917754	77917754	Human	2	name
15126460	CV690675	single nucleotide variant	NM_144573.4(NEXN):c.292T>C (p.Leu98=)	not provided [RCV000875134]	likely benign	1	77918032	77918032	Human		name
127252248	CV1067594	single nucleotide variant	NM_144573.4(NEXN):c.855G>A (p.Arg285=)	Dilated cardiomyopathy 1CC [RCV001418033]	likely benign	1	77926883	77926883	Human	1	name
127270139	CV1089327	single nucleotide variant	NM_144573.4(NEXN):c.711A>C (p.Ala237=)	Cardiovascular phenotype [RCV002368360]\|Dilated cardiomyopathy 1CC [RCV001441346]	likely benign	1	77926739	77926739	Human	2	name
127336014	CV1110850	single nucleotide variant	NM_144573.4(NEXN):c.591A>G (p.Glu197=)	Dilated cardiomyopathy 1CC [RCV001474705]	likely benign	1	77926515	77926515	Human	1	name
127288357	CV1131721	single nucleotide variant	NM_144573.4(NEXN):c.669G>A (p.Lys223=)	Dilated cardiomyopathy 1CC [RCV001495188]	likely benign	1	77926593	77926593	Human	1	name
150333249	CV1164098	single nucleotide variant	NM_144573.4(NEXN):c.67G>A (p.Val23Ile)	not provided [RCV001528775]	uncertain significance	1	77917605	77917605	Human		name
151232931	CV1320025	single nucleotide variant	NM_144573.4(NEXN):c.408G>A (p.Lys136=)	Cardiomyopathy [RCV001799381]\|Dilated cardiomyopathy 1CC [RCV002077231]	likely benign	1	77918234	77918234	Human	3	name
151232933	CV1320026	single nucleotide variant	NM_144573.4(NEXN):c.52G>A (p.Val18Ile)	Cardiomyopathy [RCV001799382]\|Cardiovascular phenotype [RCV004988751]	uncertain significance	1	77917590	77917590	Human	2	name
152151957	CV1572408	single nucleotide variant	NM_144573.4(NEXN):c.381C>A (p.Arg127=)	Dilated cardiomyopathy 1CC [RCV002139653]	likely benign	1	77918207	77918207	Human	1	name
152154055	CV1592191	deletion	NM_144573.4(NEXN):c.1252-14_1252-11del	Dilated cardiomyopathy 1CC [RCV002102678]	likely benign	1	77935806	77935809	Human	1	name
152130346	CV1630948	single nucleotide variant	NM_144573.4(NEXN):c.352A>C (p.Arg118=)	Dilated cardiomyopathy 1CC [RCV002119005]	likely benign	1	77918178	77918178	Human	1	name
152070935	CV1638689	single nucleotide variant	NM_144573.4(NEXN):c.373C>A (p.Arg125=)	Dilated cardiomyopathy 1CC [RCV002075091]	likely benign	1	77918199	77918199	Human	1	name
152039587	CV1669600	deletion	NM_144573.4(NEXN):c.137del (p.Asn46fs)	Dilated cardiomyopathy 1CC [RCV002496163]\|not provided [RCV002224501]	uncertain significance	1	77917673	77917673	Human	1	name
155673079	CV1792171	single nucleotide variant	NM_144573.4(NEXN):c.32T>C (p.Leu11Pro)	Cardiovascular phenotype [RCV002454689]	uncertain significance	1	77917570	77917570	Human		name
155717665	CV1792528	single nucleotide variant	NM_144573.4(NEXN):c.345G>A (p.Glu115=)	Cardiovascular phenotype [RCV002337477]\|Dilated cardiomyopathy 1CC [RCV003775629]	likely benign	1	77918171	77918171	Human	2	name
155672133	CV1793252	single nucleotide variant	NM_144573.4(NEXN):c.378A>G (p.Lys126=)	Cardiovascular phenotype [RCV002351192]\|Dilated cardiomyopathy 1CC [RCV003775732]	likely benign	1	77918204	77918204	Human	2	name
155707797	CV1798727	single nucleotide variant	NM_144573.4(NEXN):c.46A>G (p.Lys16Glu)	Cardiovascular phenotype [RCV002335294]	uncertain significance	1	77917584	77917584	Human		name
155743712	CV1806926	single nucleotide variant	NM_144573.4(NEXN):c.561G>A (p.Lys187=)	Cardiovascular phenotype [RCV002345007]	likely benign	1	77926485	77926485	Human		name
155736594	CV1808921	single nucleotide variant	NM_144573.4(NEXN):c.474T>C (p.Thr158=)	Cardiovascular phenotype [RCV002330624]	uncertain significance	1	77925214	77925214	Human		name
155742260	CV1809679	single nucleotide variant	NM_144573.4(NEXN):c.522A>C (p.Val174=)	Cardiovascular phenotype [RCV002344304]\|Dilated cardiomyopathy 1CC [RCV003096660]	likely benign	1	77926446	77926446	Human	2	name
155698266	CV1816872	single nucleotide variant	NM_144573.4(NEXN):c.820T>C (p.Leu274=)	Cardiovascular phenotype [RCV002427964]	likely benign	1	77926848	77926848	Human		name
155670382	CV1819166	single nucleotide variant	NM_144573.4(NEXN):c.70C>G (p.Pro24Ala)	Cardiovascular phenotype [RCV002367346]	uncertain significance	1	77917608	77917608	Human		name
155670712	CV1819253	single nucleotide variant	NM_144573.4(NEXN):c.711A>G (p.Ala237=)	Cardiovascular phenotype [RCV002367427]	likely benign	1	77926739	77926739	Human		name
155674334	CV1820388	single nucleotide variant	NM_144573.4(NEXN):c.816A>G (p.Lys272=)	Cardiovascular phenotype [RCV002421457]	likely benign	1	77926844	77926844	Human		name
155667917	CV1823943	single nucleotide variant	NM_144573.4(NEXN):c.80G>T (p.Gly27Val)	Cardiovascular phenotype [RCV002419486]	uncertain significance	1	77917618	77917618	Human		name
155730218	CV1825753	single nucleotide variant	NM_144573.4(NEXN):c.996A>G (p.Glu332=)	Cardiovascular phenotype [RCV002382970]	likely benign	1	77929447	77929447	Human		name
155690699	CV1826879	deletion	NM_144573.4(NEXN):c.142del (p.Arg48fs)	Cardiovascular phenotype [RCV002392029]	uncertain significance	1	77917678	77917678	Human		name
155675399	CV1828944	single nucleotide variant	NM_144573.4(NEXN):c.98A>G (p.Asp33Gly)	Cardiovascular phenotype [RCV002387443]\|not provided [RCV005002833]	uncertain significance	1	77917636	77917636	Human		name
156158844	CV1906751	single nucleotide variant	NM_144573.4(NEXN):c.612C>T (p.Tyr204=)	Cardiovascular phenotype [RCV004985191]\|Dilated cardiomyopathy 1CC [RCV003082812]	likely benign	1	77926536	77926536	Human	2	name
156446792	CV1948145	deletion	NM_144573.4(NEXN):c.1252-19_1252-18del	Dilated cardiomyopathy 1CC [RCV003118308]	likely benign	1	77935804	77935805	Human	1	name
156338211	CV1977005	single nucleotide variant	NM_144573.4(NEXN):c.47A>C (p.Lys16Thr)	Dilated cardiomyopathy 1CC [RCV002601142]	uncertain significance	1	77917585	77917585	Human	1	name
10055885	CV198074	single nucleotide variant	NM_144573.4(NEXN):c.62C>T (p.Thr21Ile)	not provided [RCV000183647]	uncertain significance	1	77917600	77917600	Human		name
156390272	CV1998682	single nucleotide variant	NM_144573.4(NEXN):c.789G>A (p.Lys263=)	Dilated cardiomyopathy 1CC [RCV002680695]	likely benign	1	77926817	77926817	Human	1	name
155950148	CV2084315	single nucleotide variant	NM_144573.4(NEXN):c.651A>G (p.Pro217=)	Cardiovascular phenotype [RCV003308307]\|Dilated cardiomyopathy 1CC [RCV002880454]	likely benign	1	77926575	77926575	Human	2	name
11093753	CV228513	single nucleotide variant	NM_144573.4(NEXN):c.86G>T (p.Gly29Val)	Dilated cardiomyopathy 1CC [RCV000765399]\|not specified [RCV000220183]	uncertain significance	1	77917624	77917624	Human	1	name
329364048	CV2432745	single nucleotide variant	NM_144573.4(NEXN):c.50C>G (p.Pro17Arg)	Cardiovascular phenotype [RCV003168463]	uncertain significance	1	77917588	77917588	Human		name
401777649	CV2704235	single nucleotide variant	NM_144573.4(NEXN):c.71C>T (p.Pro24Leu)	Cardiovascular phenotype [RCV004311235]	uncertain significance	1	77917609	77917609	Human		name
401777345	CV2730290	single nucleotide variant	NM_144573.4(NEXN):c.29T>G (p.Ile10Ser)	Cardiovascular phenotype [RCV003306349]	uncertain significance	1	77917567	77917567	Human		name
404978810	CV2852255	single nucleotide variant	NM_144573.4(NEXN):c.43T>C (p.Ser15Pro)	Cardiomyopathy [RCV003487251]	uncertain significance	1	77917581	77917581	Human	2	name
405051729	CV3084721	single nucleotide variant	NM_144573.4(NEXN):c.666A>G (p.Ala222=)	Dilated cardiomyopathy 1CC [RCV003798128]	likely benign	1	77926590	77926590	Human	1	name
402515015	CV3087609	single nucleotide variant	NM_144573.4(NEXN):c.972T>C (p.Asp324=)	Dilated cardiomyopathy 1CC [RCV003789960]	likely benign	1	77929423	77929423	Human	1	name
402490972	CV3091026	single nucleotide variant	NM_144573.4(NEXN):c.930C>T (p.Leu310=)	Cardiovascular phenotype [RCV004366564]\|Dilated cardiomyopathy 1CC [RCV003787530]	likely benign	1	77929381	77929381	Human	2	name
405727993	CV3391097	single nucleotide variant	NM_144573.4(NEXN):c.741G>A (p.Leu247=)	Cardiovascular phenotype [RCV004524759]	likely benign	1	77926769	77926769	Human		name
405728003	CV3391099	single nucleotide variant	NM_144573.4(NEXN):c.921T>C (p.Pro307=)	Cardiovascular phenotype [RCV004524761]\|Dilated cardiomyopathy 1CC [RCV005220936]	likely benign	1	77929372	77929372	Human	2	name
407526580	CV3451099	single nucleotide variant	NM_144573.4(NEXN):c.975A>G (p.Glu325=)	Cardiovascular phenotype [RCV004654865]	likely benign	1	77929426	77929426	Human		name
597698201	CV3565787	single nucleotide variant	NM_144573.4(NEXN):c.621T>C (p.Asp207=)	Cardiovascular phenotype [RCV004987531]	likely benign	1	77926545	77926545	Human		name
597698239	CV3565796	single nucleotide variant	NM_144573.4(NEXN):c.573T>C (p.Asp191=)	Cardiovascular phenotype [RCV004987539]	likely benign	1	77926497	77926497	Human		name
12741287	CV359367	single nucleotide variant	NM_144573.4(NEXN):c.65A>G (p.Tyr22Cys)	not specified [RCV000414636]	uncertain significance	1	77917603	77917603	Human		name
12833355	CV365381	single nucleotide variant	NM_144573.4(NEXN):c.468G>A (p.Thr156=)	Dilated cardiomyopathy 1CC [RCV001406340]\|not specified [RCV000418328]	likely benign	1	77925208	77925208	Human	1	name
597694684	CV3727076	single nucleotide variant	NM_144573.4(NEXN):c.86G>C (p.Gly29Ala)	Dilated cardiomyopathy 1CC [RCV005032825]	uncertain significance	1	77917624	77917624	Human	1	name
597836543	CV3875580	single nucleotide variant	NM_144573.4(NEXN):c.354G>A (p.Arg118=)	Dilated cardiomyopathy 1CC [RCV005225625]	likely benign	1	77918180	77918180	Human	1	name
597887074	CV3876484	single nucleotide variant	NM_144573.4(NEXN):c.810A>C (p.Ala270=)	Dilated cardiomyopathy 1CC [RCV005218230]	likely benign	1	77926838	77926838	Human	1	name
597923997	CV3877227	single nucleotide variant	NM_144573.4(NEXN):c.504A>C (p.Ser168=)	Dilated cardiomyopathy 1CC [RCV005223923]	likely benign	1	77926428	77926428	Human	1	name
616937193	CV4011116	single nucleotide variant	NM_144573.4(NEXN):c.324A>G (p.Glu108=)	not specified [RCV005404960]	likely benign	1	77918150	77918150	Human		name
12898572	CV405240	single nucleotide variant	NM_144573.4(NEXN):c.450T>A (p.Ile150=)	Cardiovascular phenotype [RCV002341153]\|not provided [RCV000478213]	uncertain significance	1	77925190	77925190	Human		name
13473679	CV442887	single nucleotide variant	NM_144573.4(NEXN):c.64T>A (p.Tyr22Asn)	Cardiovascular phenotype [RCV004984942]\|Dilated cardiomyopathy 1CC [RCV001231383]\|not provided [RCV000519442]	uncertain significance	1	77917602	77917602	Human	2	name
13533587	CV509226	deletion	NM_144573.4(NEXN):c.7_9del (p.Asp3del)	Cardiovascular phenotype [RCV000617761]\|Dilated cardiomyopathy 1CC [RCV001301572]	uncertain significance	1	77916111	77916113	Human	2	name
13592782	CV509233	single nucleotide variant	NM_144573.4(NEXN):c.739T>C (p.Leu247=)	Cardiovascular phenotype [RCV000620810]\|Dilated cardiomyopathy 1CC [RCV001462534]\|not provided [RCV001797113]	likely benign	1	77926767	77926767	Human	2	name
13620085	CV516079	single nucleotide variant	NM_144573.4(NEXN):c.507A>G (p.Leu169=)	Cardiovascular phenotype [RCV002343328]\|Dilated cardiomyopathy 1CC [RCV000647290]	likely benign	1	77926431	77926431	Human	2	name
13620088	CV516080	single nucleotide variant	NM_144573.4(NEXN):c.321T>A (p.Ala107=)	Dilated cardiomyopathy 1CC [RCV000647292]	likely benign	1	77918147	77918147	Human	1	name
8610772	CV57070	single nucleotide variant	NM_144573.4(NEXN):c.363G>A (p.Thr121=)	Cardiomyopathy [RCV000768800]\|Cardiovascular phenotype [RCV000242769]\|Dilated cardiomyopathy 1CC [RCV000231898]\|not provided [RCV001811305]\|not specified [RCV000041177]	benign\|likely benign	1	77918189	77918189	Human	4	name
8610776	CV57074	single nucleotide variant	NM_144573.4(NEXN):c.732C>A (p.Pro244=)	Cardiomyopathy [RCV000769816]\|Cardiovascular phenotype [RCV000618507]\|Dilated cardiomyopathy 1CC [RCV000458710]\|NEXN-related disorder [RCV004541207]\|not provided [RCV001529872]\|not specified [RCV000041181]	benign\|likely benign\|conflicting interpretations of pathogenicity\|uncertain significance	1	77926760	77926760	Human	4	name , trait , alternate_id
8610778	CV57076	single nucleotide variant	NM_144573.4(NEXN):c.777A>G (p.Gln259=)	Cardiovascular phenotype [RCV000620116]\|Dilated cardiomyopathy 1CC [RCV000647289]\|not provided [RCV001725956]\|not specified [RCV000041183]	benign\|likely benign\|conflicting interpretations of pathogenicity	1	77926805	77926805	Human	2	name
14688355	CV614726	single nucleotide variant	NM_144573.4(NEXN):c.60A>C (p.Lys20Asn)	Cardiomyopathy [RCV000768795]	uncertain significance	1	77917598	77917598	Human	2	name
14688766	CV614731	single nucleotide variant	NM_144573.4(NEXN):c.732C>T (p.Pro244=)	Cardiomyopathy [RCV000769817]\|Cardiovascular phenotype [RCV002386330]\|Dilated cardiomyopathy 1CC [RCV002533955]\|not specified [RCV005405300]	benign\|likely benign	1	77926760	77926760	Human	4	name
14743721	CV655127	single nucleotide variant	NM_144573.4(NEXN):c.483A>C (p.Ala161=)	not provided [RCV000842256]	likely benign	1	77925223	77925223	Human		name
15097896	CV685827	single nucleotide variant	NM_144573.4(NEXN):c.456C>T (p.Asp152=)	Cardiovascular phenotype [RCV002336812]\|Dilated cardiomyopathy 1CC [RCV002539045]	likely benign	1	77925196	77925196	Human	2	name
15156082	CV685828	single nucleotide variant	NM_144573.4(NEXN):c.492A>G (p.Glu164=)	Cardiomyopathy [RCV003486939]\|not provided [RCV000868162]	likely benign	1	77926416	77926416	Human	2	name
15098302	CV719085	single nucleotide variant	NM_144573.4(NEXN):c.579A>G (p.Glu193=)	Cardiovascular phenotype [RCV002354727]\|Dilated cardiomyopathy 1CC [RCV001483348]	likely benign	1	77926503	77926503	Human	2	name
15197664	CV762084	single nucleotide variant	NM_144573.4(NEXN):c.987A>C (p.Ala329=)	Cardiovascular phenotype [RCV003307718]\|Dilated cardiomyopathy 1CC [RCV001478204]	likely benign	1	77929438	77929438	Human	2	name
26902663	CV824421	single nucleotide variant	NM_144573.4(NEXN):c.55C>T (p.Pro19Ser)	Cardiovascular phenotype [RCV004986737]\|Dilated cardiomyopathy 1CC [RCV001036009]\|not provided [RCV004590033]	uncertain significance	1	77917593	77917593	Human	2	name
126768368	CV1003002	single nucleotide variant	NM_144573.4(NEXN):c.175G>A (p.Glu59Lys)	Cardiovascular phenotype [RCV002412032]\|Dilated cardiomyopathy 1CC [RCV001321324]	uncertain significance	1	77917713	77917713	Human	2	name
126771204	CV1003003	single nucleotide variant	NM_144573.4(NEXN):c.244G>A (p.Asp82Asn)	Dilated cardiomyopathy 1CC [RCV001323023]	uncertain significance	1	77917984	77917984	Human	1	name
126751448	CV1003005	deletion	NM_144573.4(NEXN):c.962del (p.Arg321fs)	Dilated cardiomyopathy 1CC [RCV001316118]	conflicting interpretations of pathogenicity\|uncertain significance	1	77929413	77929413	Human	1	name
126736787	CV1015789	single nucleotide variant	NM_144573.4(NEXN):c.178C>T (p.Gln60Ter)	Dilated cardiomyopathy 1CC [RCV001328615]\|not provided [RCV001773660]	uncertain significance	1	77917716	77917716	Human	1	name
126922677	CV1040322	single nucleotide variant	NM_144573.4(NEXN):c.112A>C (p.Met38Leu)	Dilated cardiomyopathy 1CC [RCV001364950]	uncertain significance	1	77917650	77917650	Human	1	name
127270160	CV1067595	single nucleotide variant	NM_144573.4(NEXN):c.1372T>C (p.Leu458=)	Dilated cardiomyopathy 1CC [RCV001404905]	likely benign	1	77935943	77935943	Human	1	name
127249364	CV1089328	single nucleotide variant	NM_144573.4(NEXN):c.1419A>G (p.Arg473=)	Cardiovascular phenotype [RCV002395973]\|Dilated cardiomyopathy 1CC [RCV001425096]\|NEXN-related disorder [RCV004531290]	likely benign	1	77935990	77935990	Human	2	name , trait , alternate_id
127232969	CV1089329	single nucleotide variant	NM_144573.4(NEXN):c.1651C>T (p.Leu551=)	Cardiovascular phenotype [RCV002395963]\|Dilated cardiomyopathy 1CC [RCV001421532]	likely benign	1	77942200	77942200	Human	2	name
127281853	CV1089330	single nucleotide variant	NM_144573.4(NEXN):c.1995T>C (p.Ser665=)	Cardiomyopathy [RCV003150431]\|Dilated cardiomyopathy 1CC [RCV001447431]\|NEXN-related disorder [RCV004533753]	likely benign	1	77942796	77942796	Human	4	name , trait , alternate_id
127314482	CV1110851	single nucleotide variant	NM_144573.4(NEXN):c.1266T>C (p.Asn422=)	Cardiovascular phenotype [RCV002377769]\|Dilated cardiomyopathy 1CC [RCV001457703]	likely benign	1	77935837	77935837	Human	2	name
127318085	CV1110852	single nucleotide variant	NM_144573.4(NEXN):c.1377T>A (p.Ser459=)	Dilated cardiomyopathy 1CC [RCV001466073]	likely benign	1	77935948	77935948	Human	1	name
127296190	CV1131722	single nucleotide variant	NM_144573.4(NEXN):c.1257G>A (p.Glu419=)	Dilated cardiomyopathy 1CC [RCV001497418]	likely benign	1	77935828	77935828	Human	1	name
127329917	CV1131723	single nucleotide variant	NM_144573.4(NEXN):c.1368A>G (p.Gly456=)	Dilated cardiomyopathy 1CC [RCV001487758]	likely benign	1	77935939	77935939	Human	1	name
127310729	CV1131724	single nucleotide variant	NM_144573.4(NEXN):c.1662A>G (p.Lys554=)	Cardiovascular phenotype [RCV002405189]\|Dilated cardiomyopathy 1CC [RCV001501436]	likely benign\|uncertain significance	1	77942463	77942463	Human	2	name
127302242	CV1131725	single nucleotide variant	NM_144573.4(NEXN):c.1950A>G (p.Gly650=)	Cardiovascular phenotype [RCV002421095]\|Dilated cardiomyopathy 1CC [RCV001478896]	likely benign	1	77942751	77942751	Human	2	name
127289175	CV1151939	duplication	NM_144573.4(NEXN):c.511dup (p.Ile171fs)	not provided [RCV001509040]	uncertain significance	1	77926434	77926435	Human		name
150532577	CV1293552	single nucleotide variant	NM_144573.4(NEXN):c.176A>G (p.Glu59Gly)	Cardiovascular phenotype [RCV003163823]\|Dilated cardiomyopathy 1CC [RCV003771915]\|not provided [RCV001757829]	uncertain significance	1	77917714	77917714	Human	2	name
150555891	CV1305391	single nucleotide variant	NM_144573.4(NEXN):c.185T>A (p.Ile62Asn)	Cardiovascular phenotype [RCV002414328]\|NEXN-related disorder [RCV004536300]\|not provided [RCV001773324]	uncertain significance	1	77917723	77917723	Human	1	name , trait , alternate_id
151232925	CV1320022	single nucleotide variant	NM_144573.4(NEXN):c.1731C>G (p.Thr577=)	Cardiomyopathy [RCV001799378]\|Cardiovascular phenotype [RCV003163936]\|Dilated cardiomyopathy 1CC [RCV002541323]	likely benign	1	77942532	77942532	Human	4	name
151232937	CV1320028	deletion	NM_144573.4(NEXN):c.817del (p.Arg273fs)	Cardiomyopathy [RCV001799384]	uncertain significance	1	77926845	77926845	Human	2	name
151871573	CV1340676	single nucleotide variant	NM_144573.4(NEXN):c.201G>A (p.Trp67Ter)	Cardiomyopathy [RCV003150468]\|Cardiovascular phenotype [RCV004641768]\|Dilated cardiomyopathy 1CC [RCV001939874]\|not provided [RCV003234134]	pathogenic\|likely pathogenic\|uncertain significance	1	77917739	77917739	Human	4	name
151837406	CV1416967	single nucleotide variant	NM_144573.4(NEXN):c.156C>A (p.Asp52Glu)	Dilated cardiomyopathy 1CC [RCV002014941]	uncertain significance	1	77917694	77917694	Human	1	name
151766128	CV1495952	single nucleotide variant	NM_144573.4(NEXN):c.190G>C (p.Glu64Gln)	Cardiovascular phenotype [RCV004988794]\|Dilated cardiomyopathy 1CC [RCV001863623]	uncertain significance	1	77917728	77917728	Human	2	name
152082255	CV1525125	single nucleotide variant	NM_144573.4(NEXN):c.1437T>G (p.Leu479=)	Dilated cardiomyopathy 1CC [RCV002130968]	likely benign	1	77936008	77936008	Human	1	name
152046129	CV1526906	single nucleotide variant	NM_144573.4(NEXN):c.1794A>G (p.Pro598=)	Dilated cardiomyopathy 1CC [RCV002166290]	likely benign	1	77942595	77942595	Human	1	name
152162969	CV1537514	single nucleotide variant	NM_144573.4(NEXN):c.1921T>C (p.Leu641=)	Cardiovascular phenotype [RCV002409527]\|Dilated cardiomyopathy 1CC [RCV002159973]	likely benign	1	77942722	77942722	Human	2	name
152121592	CV1547599	single nucleotide variant	NM_144573.4(NEXN):c.1179A>C (p.Thr393=)	Dilated cardiomyopathy 1CC [RCV002081625]	likely benign	1	77933407	77933407	Human	1	name
152155556	CV1560972	single nucleotide variant	NM_144573.4(NEXN):c.1899G>A (p.Arg633=)	Cardiovascular phenotype [RCV004045796]\|Dilated cardiomyopathy 1CC [RCV002102875]	likely benign	1	77942700	77942700	Human	2	name
152097594	CV1611566	single nucleotide variant	NM_144573.4(NEXN):c.1674G>A (p.Glu558=)	Dilated cardiomyopathy 1CC [RCV002172672]	likely benign	1	77942475	77942475	Human	1	name
9692066	CV172461	single nucleotide variant	NM_144573.4(NEXN):c.1065T>C (p.Asp355=)	Cardiomyopathy [RCV000769822]\|Cardiovascular phenotype [RCV002408670]\|Dilated cardiomyopathy 1CC [RCV002055996]\|not specified [RCV000151560]	benign\|likely benign\|uncertain significance	1	77933293	77933293	Human	4	name
9692064	CV172595	single nucleotide variant	NM_144573.4(NEXN):c.220A>C (p.Ile74Leu)	not provided [RCV004724930]\|not specified [RCV000151558]	uncertain significance	1	77917960	77917960	Human		name
9689314	CV172599	single nucleotide variant	NM_144573.4(NEXN):c.1029G>A (p.Ala343=)	Cardiovascular phenotype [RCV000620851]\|Dilated cardiomyopathy 1CC [RCV000545192]\|not provided [RCV001812130]\|not specified [RCV000154798]	benign\|likely benign\|conflicting interpretations of pathogenicity\|uncertain significance	1	77929480	77929480	Human	2	name
9692068	CV172603	single nucleotide variant	NM_144573.4(NEXN):c.1773A>G (p.Thr591=)	Cardiovascular phenotype [RCV002408671]\|not specified [RCV000151562]	likely benign	1	77942574	77942574	Human		name
9692069	CV173021	single nucleotide variant	NM_144573.4(NEXN):c.1887A>G (p.Gln629=)	Cardiovascular phenotype [RCV002408672]\|not specified [RCV000151563]	likely benign	1	77942688	77942688	Human		name
155727234	CV1822485	deletion	NM_144573.4(NEXN):c.700del (p.Glu234fs)	Cardiovascular phenotype [RCV002364821]	uncertain significance	1	77926728	77926728	Human		name
155722702	CV1828319	single nucleotide variant	NM_144573.4(NEXN):c.1677G>A (p.Glu559=)	Cardiovascular phenotype [RCV002405963]	likely benign	1	77942478	77942478	Human		name
155683869	CV1830302	single nucleotide variant	NM_144573.4(NEXN):c.1491T>C (p.Val497=)	Cardiovascular phenotype [RCV002389713]\|NEXN-related disorder [RCV004545318]	likely benign	1	77942040	77942040	Human	1	name , trait , alternate_id
155684104	CV1830344	single nucleotide variant	NM_144573.4(NEXN):c.103T>G (p.Phe35Val)	Cardiovascular phenotype [RCV002389755]	uncertain significance	1	77917641	77917641	Human		name
155724349	CV1831680	single nucleotide variant	NM_144573.4(NEXN):c.1737A>G (p.Ser579=)	Cardiovascular phenotype [RCV002399263]	likely benign	1	77942538	77942538	Human		name
155712394	CV1833302	single nucleotide variant	NM_144573.4(NEXN):c.1473G>A (p.Glu491=)	Cardiovascular phenotype [RCV002396982]	uncertain significance	1	77936044	77936044	Human		name
155745480	CV1834662	single nucleotide variant	NM_144573.4(NEXN):c.1719T>C (p.Asp573=)	Cardiovascular phenotype [RCV002414766]	likely benign	1	77942520	77942520	Human		name
155706606	CV1837208	single nucleotide variant	NM_144573.4(NEXN):c.1533G>A (p.Val511=)	Cardiovascular phenotype [RCV002403004]	likely benign	1	77942082	77942082	Human		name
155744976	CV1837842	single nucleotide variant	NM_144573.4(NEXN):c.1680G>A (p.Glu560=)	Cardiovascular phenotype [RCV002414537]	likely benign	1	77942481	77942481	Human		name
155743331	CV1839367	single nucleotide variant	NM_144573.4(NEXN):c.1839T>A (p.Ile613=)	Cardiovascular phenotype [RCV002412786]	likely benign	1	77942640	77942640	Human		name
155705712	CV1841117	single nucleotide variant	NM_144573.4(NEXN):c.227A>G (p.Glu76Gly)	Cardiovascular phenotype [RCV002446051]	uncertain significance	1	77917967	77917967	Human		name
155711752	CV1845328	single nucleotide variant	NM_144573.4(NEXN):c.247G>A (p.Glu83Lys)	Cardiovascular phenotype [RCV002430780]\|Dilated cardiomyopathy 1CC [RCV003101867]	uncertain significance	1	77917987	77917987	Human	2	name
155747987	CV1846460	single nucleotide variant	NM_144573.4(NEXN):c.2010C>A (p.Thr670=)	Cardiovascular phenotype [RCV002417336]	likely benign	1	77942811	77942811	Human		name
155671543	CV1848612	single nucleotide variant	NM_144573.4(NEXN):c.255T>G (p.Asp85Glu)	Cardiovascular phenotype [RCV002437082]	likely benign	1	77917995	77917995	Human		name
155725740	CV1851970	single nucleotide variant	NM_144573.4(NEXN):c.254A>G (p.Asp85Gly)	Cardiovascular phenotype [RCV002433288]	uncertain significance	1	77917994	77917994	Human		name
155679769	CV1853073	single nucleotide variant	NM_144573.4(NEXN):c.1113G>A (p.Pro371=)	Cardiovascular phenotype [RCV002439524]\|Dilated cardiomyopathy 1CC [RCV003102190]\|not specified [RCV005405919]	likely benign\|uncertain significance	1	77933341	77933341	Human	2	name
155683315	CV1853523	single nucleotide variant	NM_144573.4(NEXN):c.293T>A (p.Leu98Ter)	Cardiovascular phenotype [RCV002440154]	uncertain significance	1	77918033	77918033	Human		name
156128113	CV1889204	single nucleotide variant	NM_144573.4(NEXN):c.1752C>T (p.Phe584=)	Dilated cardiomyopathy 1CC [RCV003081722]	likely benign	1	77942553	77942553	Human	1	name
156148278	CV1895271	single nucleotide variant	NM_144573.4(NEXN):c.1509C>T (p.Ser503=)	Cardiovascular phenotype [RCV004636655]\|Dilated cardiomyopathy 1CC [RCV003082459]\|not specified [RCV005405961]	likely benign	1	77942058	77942058	Human	2	name
156287780	CV1900814	single nucleotide variant	NM_144573.4(NEXN):c.1200G>A (p.Lys400=)	Dilated cardiomyopathy 1CC [RCV002598625]	likely benign	1	77933428	77933428	Human	1	name
10050024	CV191294	single nucleotide variant	NM_144573.4(NEXN):c.1653A>G (p.Leu551=)	Cardiomyopathy [RCV000768805]\|Cardiovascular phenotype [RCV003298217]\|Dilated cardiomyopathy 1CC [RCV002517676]\|not provided [RCV000174419]	likely benign\|uncertain significance	1	77942202	77942202	Human	4	name
156158758	CV1928425	single nucleotide variant	NM_144573.4(NEXN):c.106G>A (p.Glu36Lys)	Cardiovascular phenotype [RCV004072125]\|Dilated cardiomyopathy 1CC [RCV002664164]	uncertain significance	1	77917644	77917644	Human	2	name
10055886	CV198075	single nucleotide variant	NM_144573.4(NEXN):c.242A>T (p.Asp81Val)	Cardiovascular phenotype [RCV002444744]\|Dilated cardiomyopathy 1CC [RCV000647282]\|Left ventricular hypertrophy [RCV000678728]\|not provided [RCV000183648]\|not specified [RCV001195577]	likely pathogenic\|likely benign\|uncertain significance	1	77917982	77917982	Human	4	name
10055909	CV198080	deletion	NM_144573.4(NEXN):c.571del (p.Asp191fs)	not provided [RCV000183677]	uncertain significance	1	77926494	77926494	Human		name
156192877	CV1994736	single nucleotide variant	NM_144573.4(NEXN):c.1839T>C (p.Ile613=)	Dilated cardiomyopathy 1CC [RCV002643367]	likely benign	1	77942640	77942640	Human	1	name
156011442	CV2075632	single nucleotide variant	NM_144573.4(NEXN):c.1182G>A (p.Glu394=)	Dilated cardiomyopathy 1CC [RCV002843895]	likely benign	1	77933410	77933410	Human	1	name
156141506	CV2082342	single nucleotide variant	NM_144573.4(NEXN):c.1411C>A (p.Arg471=)	Dilated cardiomyopathy 1CC [RCV002872000]	likely benign	1	77935982	77935982	Human	1	name
156319286	CV2165730	duplication	NM_144573.4(NEXN):c.717dup (p.Glu240fs)	Dilated cardiomyopathy 1CC [RCV003029052]	pathogenic	1	77926738	77926739	Human	1	name
156346719	CV2172689	deletion	NM_144573.4(NEXN):c.676del (p.Ser226fs)	Dilated cardiomyopathy 1CC [RCV003030600]	pathogenic	1	77926598	77926598	Human	1	name
156331326	CV2181056	single nucleotide variant	NM_144573.4(NEXN):c.1383A>G (p.Lys461=)	Dilated cardiomyopathy 1CC [RCV003047231]	likely benign	1	77935954	77935954	Human	1	name
11346404	CV238348	single nucleotide variant	NM_144573.4(NEXN):c.1089A>C (p.Thr363=)	Dilated cardiomyopathy 1CC [RCV001453702]	likely benign	1	77933317	77933317	Human	1	name
243055967	CV2416715	single nucleotide variant	NM_144573.4(NEXN):c.1527C>T (p.His509=)	Cardiomyopathy [RCV003150800]	likely benign	1	77942076	77942076	Human	2	name
243054080	CV2418412	single nucleotide variant	NM_144573.4(NEXN):c.125G>A (p.Arg42Lys)	Cardiovascular phenotype [RCV004654191]\|not provided [RCV003154438]\|not specified [RCV005240714]	uncertain significance	1	77917663	77917663	Human		name
329378785	CV2432742	single nucleotide variant	NM_144573.4(NEXN):c.1611A>G (p.Leu537=)	Cardiovascular phenotype [RCV003186929]\|Dilated cardiomyopathy 1CC [RCV005215999]	likely benign	1	77942160	77942160	Human	2	name
329378790	CV2432746	single nucleotide variant	NM_144573.4(NEXN):c.1342C>T (p.Leu448=)	Cardiovascular phenotype [RCV003186932]	likely benign	1	77935913	77935913	Human		name
11543341	CV257984	single nucleotide variant	NM_144573.4(NEXN):c.1785C>T (p.Asp595=)	Cardiovascular phenotype [RCV000242332]\|Dilated cardiomyopathy 1CC [RCV000474832]\|not provided [RCV001705398]\|not specified [RCV000424808]	benign\|likely benign	1	77942586	77942586	Human	2	name
401758225	CV2704234	single nucleotide variant	NM_144573.4(NEXN):c.104T>C (p.Phe35Ser)	Cardiovascular phenotype [RCV004311234]	uncertain significance	1	77917642	77917642	Human		name
401777341	CV2730287	single nucleotide variant	NM_144573.4(NEXN):c.1431T>C (p.Ile477=)	Cardiovascular phenotype [RCV003306346]	likely benign	1	77936002	77936002	Human		name
401777353	CV2730294	single nucleotide variant	NM_144573.4(NEXN):c.214C>A (p.Gln72Lys)	Cardiovascular phenotype [RCV003306353]	uncertain significance	1	77917752	77917752	Human		name
401882523	CV2793583	single nucleotide variant	NM_144573.4(NEXN):c.1965A>G (p.Lys655=)	Cardiovascular phenotype [RCV003385765]	likely benign	1	77942766	77942766	Human		name
401927867	CV2808971	single nucleotide variant	NM_144573.4(NEXN):c.1809T>C (p.Val603=)	not provided [RCV003406568]	likely benign	1	77942610	77942610	Human		name
404986723	CV3083672	single nucleotide variant	NM_144573.4(NEXN):c.1231C>T (p.Leu411=)	Dilated cardiomyopathy 1CC [RCV003782025]\|NEXN-related disorder [RCV004539133]	likely benign	1	77933459	77933459	Human	2	name , trait , alternate_id
405017957	CV3091652	single nucleotide variant	NM_144573.4(NEXN):c.1779T>G (p.Val593=)	Dilated cardiomyopathy 1CC [RCV003795319]	likely benign	1	77942580	77942580	Human	1	name
405042469	CV3103701	single nucleotide variant	NM_144573.4(NEXN):c.1144T>C (p.Leu382=)	Dilated cardiomyopathy 1CC [RCV003797419]	likely benign	1	77933372	77933372	Human	1	name
405040155	CV3112673	single nucleotide variant	NM_144573.4(NEXN):c.1140A>G (p.Glu380=)	Dilated cardiomyopathy 1CC [RCV003807340]	likely benign	1	77933368	77933368	Human	1	name
405042264	CV3112963	single nucleotide variant	NM_144573.4(NEXN):c.1638A>G (p.Glu546=)	Dilated cardiomyopathy 1CC [RCV003807630]	likely benign	1	77942187	77942187	Human	1	name
405080713	CV3114833	deletion	NM_144573.4(NEXN):c.798del (p.Glu267fs)	Dilated cardiomyopathy 1CC [RCV003810396]	pathogenic	1	77926826	77926826	Human	1	name
405727921	CV3391086	single nucleotide variant	NM_144573.4(NEXN):c.1566G>A (p.Lys522=)	Cardiovascular phenotype [RCV004524748]	likely benign	1	77942115	77942115	Human		name
597698189	CV3565784	single nucleotide variant	NM_144573.4(NEXN):c.148T>G (p.Ser50Ala)	Cardiovascular phenotype [RCV004987528]\|Dilated cardiomyopathy 1CC [RCV005221110]	uncertain significance	1	77917686	77917686	Human	2	name
597698192	CV3565785	single nucleotide variant	NM_144573.4(NEXN):c.235G>T (p.Ala79Ser)	Cardiovascular phenotype [RCV004987529]	uncertain significance	1	77917975	77917975	Human		name
597698205	CV3565788	single nucleotide variant	NM_144573.4(NEXN):c.1563T>A (p.Ala521=)	Cardiovascular phenotype [RCV004987532]	likely benign	1	77942112	77942112	Human		name
597698235	CV3565795	single nucleotide variant	NM_144573.4(NEXN):c.116A>G (p.Gln39Arg)	Cardiovascular phenotype [RCV004987538]	uncertain significance	1	77917654	77917654	Human		name
597698244	CV3565797	deletion	NM_144573.4(NEXN):c.984del (p.Ala329fs)	Cardiovascular phenotype [RCV004987540]	uncertain significance	1	77929433	77929433	Human		name
12837584	CV365221	single nucleotide variant	NM_144573.4(NEXN):c.1890T>C (p.Tyr630=)	not specified [RCV000425420]	likely benign	1	77942691	77942691	Human		name
12840440	CV365408	single nucleotide variant	NM_144573.4(NEXN):c.1275T>C (p.Phe425=)	Cardiovascular phenotype [RCV002374653]\|not specified [RCV000430712]	likely benign	1	77935846	77935846	Human		name
12840370	CV365411	single nucleotide variant	NM_144573.4(NEXN):c.1488T>C (p.Asp496=)	Cardiovascular phenotype [RCV000621810]\|Dilated cardiomyopathy 1CC [RCV001416988]\|NEXN-related disorder [RCV004533012]\|not specified [RCV000430578]	likely benign	1	77942037	77942037	Human	2	name , trait , alternate_id
12844235	CV365511	single nucleotide variant	NM_144573.4(NEXN):c.1806G>A (p.Thr602=)	Cardiovascular phenotype [RCV002411330]\|Dilated cardiomyopathy 1CC [RCV001470491]\|not specified [RCV000437637]	likely benign	1	77942607	77942607	Human	2	name
597920358	CV3865458	single nucleotide variant	NM_144573.4(NEXN):c.1086G>A (p.Lys362=)	Dilated cardiomyopathy 1CC [RCV005223402]	likely benign	1	77933314	77933314	Human	1	name
597847688	CV3872729	single nucleotide variant	NM_144573.4(NEXN):c.1407A>G (p.Glu469=)	Dilated cardiomyopathy 1CC [RCV005212365]	likely benign	1	77935978	77935978	Human	1	name
597848195	CV3872799	single nucleotide variant	NM_144573.4(NEXN):c.1599A>G (p.Glu533=)	Dilated cardiomyopathy 1CC [RCV005212436]	likely benign	1	77942148	77942148	Human	1	name
597874287	CV3874881	single nucleotide variant	NM_144573.4(NEXN):c.1596T>C (p.Ile532=)	Dilated cardiomyopathy 1CC [RCV005216357]	likely benign	1	77942145	77942145	Human	1	name
12889508	CV391417	single nucleotide variant	NM_144573.4(NEXN):c.1083T>C (p.Tyr361=)	Cardiovascular phenotype [RCV004639248]\|Dilated cardiomyopathy 1CC [RCV001460355]	likely benign	1	77933311	77933311	Human	2	name
598254848	CV4000592	single nucleotide variant	NM_144573.4(NEXN):c.148T>C (p.Ser50Pro)	Cardiovascular phenotype [RCV005385560]	uncertain significance	1	77917686	77917686	Human		name
598232543	CV4000594	single nucleotide variant	NM_144573.4(NEXN):c.283G>A (p.Val95Ile)	Cardiovascular phenotype [RCV005381568]	uncertain significance	1	77918023	77918023	Human		name
616936311	CV4010566	single nucleotide variant	NM_144573.4(NEXN):c.2001T>C (p.Cys667=)	not specified [RCV005403912]	likely benign	1	77942802	77942802	Human		name
13471176	CV448365	single nucleotide variant	NM_144573.4(NEXN):c.1422G>A (p.Arg474=)	Cardiomyopathy [RCV001170731]\|Dilated cardiomyopathy 1CC [RCV001506161]	benign\|likely benign\|uncertain significance	1	77935993	77935993	Human	3	name
13496774	CV448367	single nucleotide variant	NM_144573.4(NEXN):c.1743T>G (p.Ala581=)	Dilated cardiomyopathy 1CC [RCV000560591]	likely benign	1	77942544	77942544	Human	1	name
13472899	CV448433	single nucleotide variant	NM_144573.4(NEXN):c.277G>C (p.Ala93Pro)	Dilated cardiomyopathy 1CC [RCV000525133]	uncertain significance	1	77918017	77918017	Human	1	name
13492668	CV448437	single nucleotide variant	NM_144573.4(NEXN):c.1137A>G (p.Glu379=)	Dilated cardiomyopathy 1CC [RCV000557603]	likely benign	1	77933365	77933365	Human	1	name
13525030	CV498844	single nucleotide variant	NM_144573.4(NEXN):c.1042A>C (p.Arg348=)	Dilated cardiomyopathy 1CC [RCV005223048]\|not specified [RCV000602602]	likely benign	1	77929493	77929493	Human	1	name
13529820	CV509228	single nucleotide variant	NM_144573.4(NEXN):c.157G>A (p.Glu53Lys)	Cardiovascular phenotype [RCV000621991]\|Dilated cardiomyopathy 1CC [RCV001044221]\|not provided [RCV000994027]	uncertain significance	1	77917695	77917695	Human	2	name
13528763	CV509235	single nucleotide variant	NM_144573.4(NEXN):c.1332A>G (p.Gln444=)	Cardiovascular phenotype [RCV000620969]\|Dilated cardiomyopathy 1CC [RCV003767771]	likely benign	1	77935903	77935903	Human	2	name
13592793	CV509240	single nucleotide variant	NM_144573.4(NEXN):c.1704C>G (p.Gly568=)	Cardiovascular phenotype [RCV000620959]	likely benign	1	77942505	77942505	Human		name
13816683	CV557425	single nucleotide variant	NM_144573.4(NEXN):c.250G>A (p.Glu84Lys)	Cardiovascular phenotype [RCV002440547]\|Dilated cardiomyopathy 1CC [RCV000706477]\|not provided [RCV002245616]	uncertain significance	1	77917990	77917990	Human	2	name
8610755	CV57053	single nucleotide variant	NM_144573.4(NEXN):c.1368A>C (p.Gly456=)	Cardiomyopathy [RCV001798219]\|Cardiovascular phenotype [RCV002381324]\|Dilated cardiomyopathy 1CC [RCV001496600]\|NEXN-related disorder [RCV004541205]\|not provided [RCV000456926]\|not specified [RCV000041159]	likely benign	1	77935939	77935939	Human	4	name , trait , alternate_id
8610761	CV57059	single nucleotide variant	NM_144573.4(NEXN):c.1704C>T (p.Gly568=)	Cardiovascular phenotype [RCV004018908]\|Dilated cardiomyopathy 1CC [RCV000969907]\|not specified [RCV000041165]	likely benign	1	77942505	77942505	Human	2	name
8610767	CV57065	single nucleotide variant	NM_144573.4(NEXN):c.249G>C (p.Glu83Asp)	not specified [RCV000041172]	uncertain significance	1	77917989	77917989	Human		name
8610775	CV57073	deletion	NM_144573.4(NEXN):c.677del (p.Ser226fs)	not specified [RCV000041180]	uncertain significance	1	77926601	77926601	Human		name
14688360	CV614729	single nucleotide variant	NM_144573.4(NEXN):c.257T>C (p.Val86Ala)	Cardiomyopathy [RCV000768799]	uncertain significance	1	77917997	77917997	Human	2	name
14688779	CV614736	single nucleotide variant	NM_144573.4(NEXN):c.1605A>G (p.Gln535=)	Cardiomyopathy [RCV000769830]\|Cardiovascular phenotype [RCV002397537]\|Dilated cardiomyopathy 1CC [RCV001460953]	likely benign	1	77942154	77942154	Human	4	name
14688367	CV614738	single nucleotide variant	NM_144573.4(NEXN):c.1770C>T (p.Asn590=)	Cardiomyopathy [RCV000768807]\|Cardiovascular phenotype [RCV004027217]	likely benign\|uncertain significance	1	77942571	77942571	Human	2	name
14720515	CV628260	single nucleotide variant	NM_144573.4(NEXN):c.134G>T (p.Arg45Ile)	Dilated cardiomyopathy 1CC [RCV000796675]	uncertain significance	1	77917672	77917672	Human	1	name
14975382	CV672382	single nucleotide variant	NM_144573.4(NEXN):c.1593A>G (p.Arg531=)	not provided [RCV000845344]	likely benign	1	77942142	77942142	Human		name
15152003	CV685829	single nucleotide variant	NM_144573.4(NEXN):c.1450C>A (p.Arg484=)	Cardiovascular phenotype [RCV003169140]\|Dilated cardiomyopathy 1CC [RCV000867357]	likely benign	1	77936021	77936021	Human	2	name
15153465	CV719086	single nucleotide variant	NM_144573.4(NEXN):c.1809T>G (p.Val603=)	not provided [RCV000880014]	likely benign	1	77942610	77942610	Human		name
15135719	CV732606	single nucleotide variant	NM_144573.4(NEXN):c.1938A>C (p.Pro646=)	not provided [RCV000898507]	likely benign	1	77942739	77942739	Human		name
15133523	CV746651	single nucleotide variant	NM_144573.4(NEXN):c.1401A>T (p.Ile467=)	Dilated cardiomyopathy 1CC [RCV000920530]	likely benign	1	77935972	77935972	Human	1	name
15146079	CV762085	single nucleotide variant	NM_144573.4(NEXN):c.1413A>G (p.Arg471=)	Dilated cardiomyopathy 1CC [RCV001452979]	likely benign	1	77935984	77935984	Human	1	name
15123810	CV762086	single nucleotide variant	NM_144573.4(NEXN):c.1533G>T (p.Val511=)	Dilated cardiomyopathy 1CC [RCV001500625]	likely benign	1	77942082	77942082	Human	1	name
28894903	CV903741	single nucleotide variant	NM_144573.4(NEXN):c.1683A>G (p.Glu561=)	Cardiomyopathy [RCV001170735]\|Cardiovascular phenotype [RCV004639489]\|Dilated cardiomyopathy 1CC [RCV002068047]\|not specified [RCV005405504]	likely benign	1	77942484	77942484	Human	4	name
38473080	CV942103	single nucleotide variant	NM_144573.4(NEXN):c.244G>C (p.Asp82His)	Dilated cardiomyopathy 1CC [RCV001231760]	uncertain significance	1	77917984	77917984	Human	1	name
126742920	CV1003004	single nucleotide variant	NM_144573.4(NEXN):c.889G>C (p.Asp297His)	Dilated cardiomyopathy 1CC [RCV001314726]	uncertain significance	1	77929340	77929340	Human	1	name
126757576	CV1003006	deletion	NM_144573.4(NEXN):c.1302del (p.Ile435fs)	Dilated cardiomyopathy 1CC [RCV001317526]\|Heart failure [RCV005235562]	pathogenic\|likely pathogenic\|uncertain significance	1	77935873	77935873	Human	3	name
126766978	CV1003008	deletion	NM_144573.4(NEXN):c.1502del (p.Arg501fs)	Cardiovascular phenotype [RCV002395699]\|Dilated cardiomyopathy 1CC [RCV001320664]	pathogenic\|uncertain significance	1	77942051	77942051	Human	2	name
126736793	CV1015790	single nucleotide variant	NM_144573.4(NEXN):c.859C>T (p.Gln287Ter)	Cardiovascular phenotype [RCV002447385]\|Dilated cardiomyopathy 1CC [RCV001328616]	uncertain significance	1	77926887	77926887	Human	1	name
126734236	CV1019427	single nucleotide variant	NM_144573.4(NEXN):c.991G>T (p.Glu331Ter)	Cardiovascular phenotype [RCV004988553]\|Dilated cardiomyopathy 1CC [RCV002547327]\|Hypertrophic cardiomyopathy 20 [RCV001334547]\|not provided [RCV002223302]	pathogenic\|uncertain significance	1	77929442	77929442	Human	2	name
126745211	CV1023494	single nucleotide variant	NM_144573.4(NEXN):c.772A>G (p.Arg258Gly)	Cardiovascular phenotype [RCV004988579]\|Dilated cardiomyopathy 1CC [RCV001351379]	uncertain significance	1	77926800	77926800	Human	2	name
126908719	CV1040323	single nucleotide variant	NM_144573.4(NEXN):c.696A>T (p.Glu232Asp)	Cardiovascular phenotype [RCV002368189]\|Dilated cardiomyopathy 1CC [RCV001368086]	uncertain significance	1	77926724	77926724	Human	2	name
126920830	CV1040324	single nucleotide variant	NM_144573.4(NEXN):c.935T>A (p.Leu312His)	Dilated cardiomyopathy 1CC [RCV001374038]\|not provided [RCV001700994]	uncertain significance	1	77929386	77929386	Human	1	name
126919938	CV1040325	single nucleotide variant	NM_144573.4(NEXN):c.946G>A (p.Glu316Lys)	Dilated cardiomyopathy 1CC [RCV001362579]	uncertain significance	1	77929397	77929397	Human	1	name
150428149	CV1186238	deletion	NM_144573.4(NEXN):c.1473+115_1473+119del	not provided [RCV001561880]	likely benign	1	77936157	77936161	Human		name
150488908	CV1274420	single nucleotide variant	NM_144573.4(NEXN):c.530A>T (p.Lys177Ile)	not provided [RCV001699983]	uncertain significance	1	77926454	77926454	Human		name
150553067	CV1298083	duplication	NM_144573.4(NEXN):c.1878dup (p.Asp627fs)	Left ventricular noncompaction cardiomyopathy [RCV001821979]\|not provided [RCV001768696]	likely pathogenic\|uncertain significance	1	77942677	77942678	Human	2	name
150553147	CV1298176	single nucleotide variant	NM_144573.4(NEXN):c.436A>G (p.Arg146Gly)	not provided [RCV001768789]	uncertain significance	1	77918262	77918262	Human		name
150553251	CV1298292	single nucleotide variant	NM_144573.4(NEXN):c.582A>T (p.Lys194Asn)	not provided [RCV001768906]	uncertain significance	1	77926506	77926506	Human		name
150554006	CV1298413	single nucleotide variant	NM_144573.4(NEXN):c.967G>A (p.Glu323Lys)	Cardiomyopathy [RCV003487001]\|Cardiovascular phenotype [RCV002370277]\|Dilated cardiomyopathy 1CC [RCV002496088]\|not provided [RCV001770612]	uncertain significance	1	77929418	77929418	Human	4	name
150530859	CV1299146	single nucleotide variant	NM_144573.4(NEXN):c.916C>T (p.Arg306Cys)	Cardiomyopathy [RCV001799124]\|Cardiovascular phenotype [RCV002449416]\|Dilated cardiomyopathy 1CC [RCV002477954]\|not provided [RCV001756839]	uncertain significance	1	77929367	77929367	Human	4	name
150552489	CV1301472	single nucleotide variant	NM_144573.4(NEXN):c.644A>G (p.Gln215Arg)	Cardiovascular phenotype [RCV002361033]\|not provided [RCV001767882]	uncertain significance	1	77926568	77926568	Human		name
150543038	CV1315065	single nucleotide variant	NM_144573.4(NEXN):c.595A>G (p.Lys199Glu)	Cardiovascular phenotype [RCV003296176]	likely pathogenic\|uncertain significance	1	77926519	77926519	Human		name
151235851	CV1319278	single nucleotide variant	NM_144573.4(NEXN):c.785G>A (p.Arg262Gln)	Cardiovascular phenotype [RCV004040855]\|Dilated cardiomyopathy 1CC [RCV001868897]\|not provided [RCV001797223]	uncertain significance	1	77926813	77926813	Human	2	name
151232936	CV1320027	single nucleotide variant	NM_144573.4(NEXN):c.685A>G (p.Met229Val)	Cardiomyopathy [RCV001799383]	uncertain significance	1	77926609	77926609	Human	2	name
151232940	CV1320029	single nucleotide variant	NM_144573.4(NEXN):c.821T>C (p.Leu274Ser)	Cardiomyopathy [RCV001799385]	uncertain significance	1	77926849	77926849	Human	2	name
151751573	CV1357323	single nucleotide variant	NM_144573.4(NEXN):c.328G>C (p.Glu110Gln)	Cardiovascular phenotype [RCV002449485]\|Dilated cardiomyopathy 1CC [RCV001894384]	uncertain significance	1	77918154	77918154	Human	2	name
151750609	CV1377646	single nucleotide variant	NM_144573.4(NEXN):c.783C>G (p.Asn261Lys)	Cardiovascular phenotype [RCV002407077]\|Dilated cardiomyopathy 1CC [RCV001948103]	uncertain significance	1	77926811	77926811	Human	2	name
151765160	CV1407758	single nucleotide variant	NM_144573.4(NEXN):c.364G>C (p.Glu122Gln)	Cardiovascular phenotype [RCV004038899]\|Dilated cardiomyopathy 1CC [RCV002044705]	uncertain significance	1	77918190	77918190	Human	2	name
151759100	CV1411069	single nucleotide variant	NM_144573.4(NEXN):c.989A>C (p.Glu330Ala)	Dilated cardiomyopathy 1CC [RCV002007647]	uncertain significance	1	77929440	77929440	Human	1	name
151819585	CV1450054	single nucleotide variant	NM_144573.4(NEXN):c.422G>A (p.Arg141His)	Cardiovascular phenotype [RCV002331383]\|Dilated cardiomyopathy 1CC [RCV001879084]	uncertain significance	1	77918248	77918248	Human	2	name
151769405	CV1454204	single nucleotide variant	NM_144573.4(NEXN):c.797C>G (p.Ala266Gly)	Cardiovascular phenotype [RCV002423080]\|Dilated cardiomyopathy 1CC [RCV001950010]	uncertain significance	1	77926825	77926825	Human	2	name
151788374	CV1479265	single nucleotide variant	NM_144573.4(NEXN):c.914A>G (p.Tyr305Cys)	Cardiovascular phenotype [RCV002370357]\|Dilated cardiomyopathy 1CC [RCV002046855]	uncertain significance	1	77929365	77929365	Human	2	name
151829698	CV1491577	single nucleotide variant	NM_144573.4(NEXN):c.790A>C (p.Lys264Gln)	Dilated cardiomyopathy 1CC [RCV002030677]	uncertain significance	1	77926818	77926818	Human	1	name
152034413	CV1669508	single nucleotide variant	NM_144573.4(NEXN):c.646C>T (p.Arg216Ter)	Dilated cardiomyopathy 1CC [RCV003327554]\|not provided [RCV002223499]	uncertain significance	1	77926570	77926570	Human	1	name
152981664	CV1676973	duplication	NM_144573.4(NEXN):c.1399dup (p.Ile467fs)	not specified [RCV002248040]	uncertain significance	1	77935963	77935964	Human		name
9690128	CV172597	single nucleotide variant	NM_144573.4(NEXN):c.586C>T (p.Arg196Cys)	Cardiomyopathy [RCV000768803]\|Cardiovascular phenotype [RCV002354374]\|Dilated cardiomyopathy 1CC [RCV000647286]\|Primary dilated cardiomyopathy [RCV002221204]\|not provided [RCV001582631]\|not specified [RCV000155781]	uncertain significance	1	77926510	77926510	Human	5	name
9690032	CV172598	single nucleotide variant	NM_144573.4(NEXN):c.949A>C (p.Met317Leu)	Cardiomyopathy [RCV001170727]\|Cardiovascular phenotype [RCV002372017]\|Dilated cardiomyopathy 1CC [RCV000647288]\|not provided [RCV001697084]\|not specified [RCV000155677]	benign\|likely benign\|uncertain significance	1	77929400	77929400	Human	4	name
9832460	CV178470	deletion	NM_144573.4(NEXN):c.1630del (p.Gln544fs)	Primary dilated cardiomyopathy [RCV000157393]	uncertain significance	1	77942179	77942179	Human	1	name
155708418	CV1785200	single nucleotide variant	NM_144573.4(NEXN):c.320C>T (p.Ala107Val)	Cardiovascular phenotype [RCV002324575]	uncertain significance	1	77918146	77918146	Human		name
155704418	CV1787592	single nucleotide variant	NM_144573.4(NEXN):c.408G>T (p.Lys136Asn)	Cardiovascular phenotype [RCV002323219]	uncertain significance	1	77918234	77918234	Human		name
155702302	CV1790471	single nucleotide variant	NM_144573.4(NEXN):c.403G>A (p.Glu135Lys)	Cardiovascular phenotype [RCV002359592]	uncertain significance	1	77918229	77918229	Human		name
155741339	CV1790747	single nucleotide variant	NM_144573.4(NEXN):c.416T>C (p.Ile139Thr)	Cardiovascular phenotype [RCV002333393]\|Dilated cardiomyopathy 1CC [RCV003094559]	uncertain significance	1	77918242	77918242	Human	2	name
155695617	CV1793012	single nucleotide variant	NM_144573.4(NEXN):c.362C>T (p.Thr121Met)	Cardiovascular phenotype [RCV002460325]\|Dilated cardiomyopathy 1CC [RCV003094269]	uncertain significance	1	77918188	77918188	Human	2	name
155695591	CV1793868	single nucleotide variant	NM_144573.4(NEXN):c.399G>A (p.Met133Ile)	Cardiovascular phenotype [RCV002357783]	uncertain significance	1	77918225	77918225	Human		name
155738915	CV1794129	single nucleotide variant	NM_144573.4(NEXN):c.431C>G (p.Ala144Gly)	Cardiovascular phenotype [RCV002332020]\|not provided [RCV005412400]	uncertain significance	1	77918257	77918257	Human		name
155739839	CV1799219	single nucleotide variant	NM_144573.4(NEXN):c.494G>C (p.Gly165Ala)	Cardiovascular phenotype [RCV002342725]	uncertain significance	1	77926418	77926418	Human		name
155733731	CV1802124	single nucleotide variant	NM_144573.4(NEXN):c.487G>C (p.Glu163Gln)	Cardiovascular phenotype [RCV002340473]	uncertain significance	1	77925227	77925227	Human		name
155738197	CV1805056	single nucleotide variant	NM_144573.4(NEXN):c.457A>G (p.Ile153Val)	Cardiovascular phenotype [RCV002342180]	uncertain significance	1	77925197	77925197	Human		name
155679596	CV1806992	single nucleotide variant	NM_144573.4(NEXN):c.583G>C (p.Glu195Gln)	Cardiovascular phenotype [RCV002353280]	uncertain significance	1	77926507	77926507	Human		name
155680475	CV1807224	single nucleotide variant	NM_144573.4(NEXN):c.587G>A (p.Arg196His)	Cardiovascular phenotype [RCV002353513]	uncertain significance	1	77926511	77926511	Human		name
155705404	CV1811194	single nucleotide variant	NM_144573.4(NEXN):c.609G>C (p.Lys203Asn)	Cardiovascular phenotype [RCV002360121]\|not provided [RCV003232613]	uncertain significance	1	77926533	77926533	Human		name
155673936	CV1811328	single nucleotide variant	NM_144573.4(NEXN):c.634T>C (p.Tyr212His)	Cardiovascular phenotype [RCV002368978]	uncertain significance	1	77926558	77926558	Human		name
155706740	CV1815315	single nucleotide variant	NM_144573.4(NEXN):c.685A>C (p.Met229Leu)	Cardiovascular phenotype [RCV002377995]	uncertain significance	1	77926609	77926609	Human		name
155728872	CV1823411	single nucleotide variant	NM_144573.4(NEXN):c.769C>A (p.Gln257Lys)	Cardiovascular phenotype [RCV002400551]	uncertain significance	1	77926797	77926797	Human		name
155705164	CV1824078	single nucleotide variant	NM_144573.4(NEXN):c.842T>C (p.Phe281Ser)	Cardiovascular phenotype [RCV002445909]	uncertain significance	1	77926870	77926870	Human		name
155729843	CV1829108	single nucleotide variant	NM_144573.4(NEXN):c.994G>A (p.Glu332Lys)	Cardiovascular phenotype [RCV002382916]	uncertain significance	1	77929445	77929445	Human		name
155796476	CV1861869	deletion	NM_144573.4(NEXN):c.1814del (p.Val605fs)	not specified [RCV002470151]	uncertain significance	1	77942615	77942615	Human		name
156318550	CV1876124	single nucleotide variant	NM_144573.4(NEXN):c.524C>G (p.Pro175Arg)	Dilated cardiomyopathy 1CC [RCV003062909]	uncertain significance	1	77926448	77926448	Human	1	name
156124522	CV1930319	single nucleotide variant	NM_144573.4(NEXN):c.345G>T (p.Glu115Asp)	Dilated cardiomyopathy 1CC [RCV002640458]	uncertain significance	1	77918171	77918171	Human	1	name
156448506	CV1950789	single nucleotide variant	NM_144573.4(NEXN):c.362C>A (p.Thr121Lys)	Dilated cardiomyopathy 1CC [RCV003120068]	uncertain significance	1	77918188	77918188	Human	1	name
156217388	CV1963401	single nucleotide variant	NM_144573.4(NEXN):c.934C>T (p.Leu312Phe)	Dilated cardiomyopathy 1CC [RCV002575387]	uncertain significance	1	77929385	77929385	Human	1	name
10055887	CV198076	single nucleotide variant	NM_144573.4(NEXN):c.442G>A (p.Glu148Lys)	not provided [RCV000183650]	uncertain significance	1	77918268	77918268	Human		name
10055888	CV198078	single nucleotide variant	NM_144573.4(NEXN):c.512T>C (p.Ile171Thr)	Cardiomyopathy [RCV000768801]\|Cardiovascular phenotype [RCV000619570]\|Dilated cardiomyopathy 1CC [RCV000542710]\|not provided [RCV001701784]\|not specified [RCV000183651]	benign\|likely benign\|conflicting interpretations of pathogenicity\|uncertain significance	1	77926436	77926436	Human	4	name
10055889	CV198079	single nucleotide variant	NM_144573.4(NEXN):c.542C>A (p.Thr181Lys)	not provided [RCV000183652]	uncertain significance	1	77926466	77926466	Human		name
10055890	CV198082	single nucleotide variant	NM_144573.4(NEXN):c.856C>T (p.Arg286Trp)	Cardiomyopathy [RCV001170498]\|Cardiovascular phenotype [RCV000252316]\|Dilated cardiomyopathy 1CC [RCV000456476]\|Primary familial hypertrophic cardiomyopathy [RCV000623726]\|not provided [RCV001704885]	benign\|likely benign\|uncertain significance	1	77926884	77926884	Human	6	name
10055913	CV198083	single nucleotide variant	NM_144573.4(NEXN):c.874G>A (p.Asp292Asn)	Cardiomyopathy [RCV001170726]\|Cardiovascular phenotype [RCV003298241]\|Dilated cardiomyopathy 1CC [RCV001852366]\|not provided [RCV000183684]	uncertain significance	1	77929325	77929325	Human	4	name
156132055	CV1998536	single nucleotide variant	NM_144573.4(NEXN):c.419A>G (p.Gln140Arg)	Dilated cardiomyopathy 1CC [RCV002663257]	uncertain significance	1	77918245	77918245	Human	1	name
156375190	CV2049363	deletion	NM_144573.4(NEXN):c.1170del (p.Lys390fs)	Dilated cardiomyopathy 1CC [RCV002814634]	pathogenic	1	77933394	77933394	Human	1	name
156226983	CV2064386	single nucleotide variant	NM_144573.4(NEXN):c.761T>C (p.Leu254Pro)	Dilated cardiomyopathy 1CC [RCV002829905]	uncertain significance	1	77926789	77926789	Human	1	name
156099669	CV2087933	single nucleotide variant	NM_144573.4(NEXN):c.314G>C (p.Arg105Thr)	Dilated cardiomyopathy 1CC [RCV002848034]	uncertain significance	1	77918140	77918140	Human	1	name
156112862	CV2104475	single nucleotide variant	NM_144573.4(NEXN):c.467C>T (p.Thr156Met)	Cardiovascular phenotype [RCV003308338]\|Dilated cardiomyopathy 1CC [RCV002927505]	uncertain significance	1	77925207	77925207	Human	2	name
155961562	CV2131892	single nucleotide variant	NM_144573.4(NEXN):c.730C>T (p.Pro244Ser)	Cardiovascular phenotype [RCV003170801]\|Dilated cardiomyopathy 1CC [RCV002995182]	uncertain significance	1	77926758	77926758	Human	2	name
155993700	CV2147775	deletion	NM_144573.4(NEXN):c.1930del (p.Thr644fs)	Dilated cardiomyopathy 1CC [RCV003016950]	uncertain significance	1	77942729	77942729	Human	1	name
156115476	CV2150496	single nucleotide variant	NM_144573.4(NEXN):c.802G>C (p.Glu268Gln)	Dilated cardiomyopathy 1CC [RCV003021583]	uncertain significance	1	77926830	77926830	Human	1	name
11094097	CV228515	single nucleotide variant	NM_144573.4(NEXN):c.379C>T (p.Arg127Cys)	Cardiovascular phenotype [RCV002354610]\|Dilated cardiomyopathy 1CC [RCV000704647]\|not provided [RCV001762462]\|not specified [RCV000220615]	uncertain significance	1	77918205	77918205	Human	2	name
11088986	CV228516	single nucleotide variant	NM_144573.4(NEXN):c.836G>A (p.Arg279His)	Cardiovascular phenotype [RCV003165544]\|Dilated cardiomyopathy 1CC [RCV002478770]\|not provided [RCV003736650]\|not specified [RCV000214249]	uncertain significance	1	77926864	77926864	Human	2	name
11091394	CV228517	single nucleotide variant	NM_144573.4(NEXN):c.864G>T (p.Met288Ile)	Cardiovascular phenotype [RCV002444863]\|Dilated cardiomyopathy 1CC [RCV002494571]\|not specified [RCV000217251]	uncertain significance	1	77926892	77926892	Human	2	name
243059137	CV2416601	single nucleotide variant	NM_144573.4(NEXN):c.337A>G (p.Arg113Gly)	Cardiomyopathy [RCV003150686]	uncertain significance	1	77918163	77918163	Human	2	name
329384764	CV2426308	single nucleotide variant	NM_144573.4(NEXN):c.980G>T (p.Arg327Met)	Cardiovascular phenotype [RCV003176882]	uncertain significance	1	77929431	77929431	Human		name
329378786	CV2432743	duplication	NM_144573.4(NEXN):c.2001dup (p.Ile668fs)	Cardiovascular phenotype [RCV003186930]	uncertain significance	1	77942801	77942802	Human		name
329378791	CV2432747	single nucleotide variant	NM_144573.4(NEXN):c.345G>C (p.Glu115Asp)	Cardiovascular phenotype [RCV003186933]	uncertain significance	1	77918171	77918171	Human		name
329364050	CV2432750	deletion	NM_144573.4(NEXN):c.1400del (p.Ile467fs)	Cardiovascular phenotype [RCV003168464]	uncertain significance	1	77935971	77935971	Human		name
329364051	CV2432752	single nucleotide variant	NM_144573.4(NEXN):c.561G>T (p.Lys187Asn)	Cardiovascular phenotype [RCV003168465]	uncertain significance	1	77926485	77926485	Human		name
329359999	CV2446515	single nucleotide variant	NM_144573.4(NEXN):c.388G>A (p.Glu130Lys)	Cardiovascular phenotype [RCV004251416]	uncertain significance	1	77918214	77918214	Human		name
11545517	CV257981	single nucleotide variant	NM_144573.4(NEXN):c.392A>C (p.Gln131Pro)	Cardiovascular phenotype [RCV000245242]\|Dilated cardiomyopathy 1CC [RCV000817176]	uncertain significance	1	77918218	77918218	Human	2	name
11547229	CV257982	single nucleotide variant	NM_144573.4(NEXN):c.817C>T (p.Arg273Cys)	Cardiovascular phenotype [RCV000247492]\|Dilated cardiomyopathy 1CC [RCV002503955]\|not provided [RCV001566404]	uncertain significance	1	77926845	77926845	Human	2	name
11546597	CV257983	single nucleotide variant	NM_144573.4(NEXN):c.634T>A (p.Tyr212Asn)	Cardiovascular phenotype [RCV000246666]\|Dilated cardiomyopathy 1CC [RCV001859448]\|not specified [RCV003330606]	likely benign\|uncertain significance	1	77926558	77926558	Human	2	name
401782907	CV2707585	single nucleotide variant	NM_144573.4(NEXN):c.635A>T (p.Tyr212Phe)	Cardiovascular phenotype [RCV004306529]	uncertain significance	1	77926559	77926559	Human		name
401861623	CV2779958	single nucleotide variant	NM_144573.4(NEXN):c.901A>G (p.Ile301Val)	Cardiovascular phenotype [RCV004353551]	uncertain significance	1	77929352	77929352	Human		name
11654511	CV281225	single nucleotide variant	NM_144573.3(NEXN):c.593A>T (p.Glu198Val)	Dilated Cardiomyopathy, Dominant [RCV000374872]\|Hypertrophic cardiomyopathy [RCV000317982]	uncertain significance	1	77926517	77926517	Human	1	name
11647778	CV283296	single nucleotide variant	NM_144573.4(NEXN):c.671G>A (p.Cys224Tyr)	Dilated cardiomyopathy 1CC [RCV000477809]	uncertain significance	1	77926595	77926595	Human	1	name
402514626	CV3087577	single nucleotide variant	NM_144573.4(NEXN):c.919C>A (p.Pro307Thr)	Dilated cardiomyopathy 1CC [RCV003789928]	uncertain significance	1	77929370	77929370	Human	1	name
404979061	CV3099329	single nucleotide variant	NM_144573.4(NEXN):c.298G>T (p.Gly100Ter)	Dilated cardiomyopathy 1CC [RCV003791157]	pathogenic	1	77918038	77918038	Human	1	name
405004135	CV3102179	duplication	NM_144573.4(NEXN):c.1536dup (p.Met513fs)	Dilated cardiomyopathy 1CC [RCV003804225]	pathogenic	1	77942084	77942085	Human	1	name
405057709	CV3102424	single nucleotide variant	NM_144573.4(NEXN):c.803A>G (p.Glu268Gly)	Dilated cardiomyopathy 1CC [RCV003798566]	uncertain significance	1	77926831	77926831	Human	1	name
405727964	CV3391093	single nucleotide variant	NM_144573.4(NEXN):c.311G>A (p.Gly104Asp)	Cardiovascular phenotype [RCV004524755]	uncertain significance	1	77918137	77918137	Human		name
405727972	CV3391094	single nucleotide variant	NM_144573.4(NEXN):c.498T>A (p.Asp166Glu)	Cardiovascular phenotype [RCV004524756]\|not provided [RCV004801442]	uncertain significance	1	77926422	77926422	Human		name
405727981	CV3391095	single nucleotide variant	NM_144573.4(NEXN):c.541A>G (p.Thr181Ala)	Cardiovascular phenotype [RCV004524757]	uncertain significance	1	77926465	77926465	Human		name
405727987	CV3391096	single nucleotide variant	NM_144573.4(NEXN):c.647G>A (p.Arg216Gln)	Cardiovascular phenotype [RCV004524758]	likely benign	1	77926571	77926571	Human		name
405727998	CV3391098	single nucleotide variant	NM_144573.4(NEXN):c.892A>G (p.Thr298Ala)	Cardiovascular phenotype [RCV004524760]	likely benign	1	77929343	77929343	Human		name
407483394	CV3414298	single nucleotide variant	NM_144573.4(NEXN):c.834G>C (p.Lys278Asn)	Hypertrophic cardiomyopathy 2 [RCV004596634]	not provided	1	77926862	77926862	Human		name
407526578	CV3451097	single nucleotide variant	NM_144573.4(NEXN):c.598G>C (p.Glu200Gln)	Cardiovascular phenotype [RCV004654864]	uncertain significance	1	77926522	77926522	Human		name
408368543	CV3513440	single nucleotide variant	NM_144573.4(NEXN):c.763G>A (p.Glu255Lys)	NEXN-related disorder [RCV004735282]	uncertain significance	1	77926791	77926791	Human		name , trait , alternate_id
408381237	CV3523803	single nucleotide variant	NM_144573.4(NEXN):c.538A>C (p.Lys180Gln)	not provided [RCV004766201]	uncertain significance	1	77926462	77926462	Human		name
597698198	CV3565786	single nucleotide variant	NM_144573.4(NEXN):c.506T>C (p.Leu169Pro)	Cardiovascular phenotype [RCV004987530]	uncertain significance	1	77926430	77926430	Human		name
597698252	CV3565799	single nucleotide variant	NM_144573.4(NEXN):c.601A>T (p.Arg201Trp)	Cardiovascular phenotype [RCV004987542]	uncertain significance	1	77926525	77926525	Human		name
597698269	CV3565803	single nucleotide variant	NM_144573.4(NEXN):c.993A>C (p.Glu331Asp)	Cardiovascular phenotype [RCV004987546]	uncertain significance	1	77929444	77929444	Human		name
597698273	CV3565804	single nucleotide variant	NM_144573.4(NEXN):c.386T>C (p.Ile129Thr)	Cardiovascular phenotype [RCV004987547]	uncertain significance	1	77918212	77918212	Human		name
597841384	CV3873716	single nucleotide variant	NM_144573.4(NEXN):c.527T>C (p.Val176Ala)	Dilated cardiomyopathy 1CC [RCV005226543]	uncertain significance	1	77926451	77926451	Human	1	name
12885542	CV391545	single nucleotide variant	NM_144573.4(NEXN):c.902T>A (p.Ile301Asn)	Cardiovascular phenotype [RCV002374780]\|Dilated cardiomyopathy 1CC [RCV000465558]\|not provided [RCV001591092]	likely benign\|uncertain significance	1	77929353	77929353	Human	2	name
8568721	CV39950	single nucleotide variant	NM_144573.4(NEXN):c.391C>G (p.Gln131Glu)	Hypertrophic cardiomyopathy 20 [RCV000023984]	pathogenic\|likely pathogenic	1	77918217	77918217	Human	1	name
8568722	CV39951	single nucleotide variant	NM_144573.4(NEXN):c.835C>T (p.Arg279Cys)	Cardiomyopathy [RCV000769818]\|Cardiovascular phenotype [RCV004017264]\|Dilated cardiomyopathy 1CC [RCV000460527]\|Hypertrophic cardiomyopathy 20 [RCV000023985]\|NEXN-related disorder [RCV004532402]\|Primary familial hypertrophic cardiomyopathy [RCV000143936]\|not pro ... (more) vided [RCV001719699]\|not specified [RCV000041184]	pathogenic\|benign\|likely benign\|conflicting interpretations of pathogenicity\|uncertain significance	1	77926863	77926863	Human	6	name , trait , alternate_id
598254846	CV4000588	single nucleotide variant	NM_144573.4(NEXN):c.716A>G (p.Lys239Arg)	Cardiovascular phenotype [RCV005385559]	uncertain significance	1	77926744	77926744	Human		name
598232529	CV4000589	single nucleotide variant	NM_144573.4(NEXN):c.950T>C (p.Met317Thr)	Cardiovascular phenotype [RCV005381564]	uncertain significance	1	77929401	77929401	Human		name
598232536	CV4000591	single nucleotide variant	NM_144573.4(NEXN):c.558A>T (p.Lys186Asn)	Cardiovascular phenotype [RCV005381566]	uncertain significance	1	77926482	77926482	Human		name
598232541	CV4000593	single nucleotide variant	NM_144573.4(NEXN):c.686T>A (p.Met229Lys)	Cardiovascular phenotype [RCV005381567]	uncertain significance	1	77926610	77926610	Human		name
598232550	CV4000597	single nucleotide variant	NM_144573.4(NEXN):c.952G>C (p.Glu318Gln)	Cardiovascular phenotype [RCV005381570]	uncertain significance	1	77929403	77929403	Human		name
598254852	CV4000599	single nucleotide variant	NM_144573.4(NEXN):c.773G>T (p.Arg258Ile)	Cardiovascular phenotype [RCV005385562]	uncertain significance	1	77926801	77926801	Human		name
598232554	CV4000600	single nucleotide variant	NM_144573.4(NEXN):c.586C>A (p.Arg196Ser)	Cardiovascular phenotype [RCV005381572]	uncertain significance	1	77926510	77926510	Human		name
598232559	CV4000601	single nucleotide variant	NM_144573.4(NEXN):c.873A>T (p.Glu291Asp)	Cardiovascular phenotype [RCV005381573]	uncertain significance	1	77929324	77929324	Human		name
598232566	CV4000603	single nucleotide variant	NM_144573.4(NEXN):c.555G>C (p.Met185Ile)	Cardiovascular phenotype [RCV005381575]	likely benign	1	77926479	77926479	Human		name
617153288	CV4018608	single nucleotide variant	NM_144573.4(NEXN):c.868A>G (p.Asn290Asp)	not specified [RCV005418870]	uncertain significance	1	77929319	77929319	Human		name
13212300	CV425384	single nucleotide variant	NM_144573.4(NEXN):c.680T>C (p.Leu227Ser)	Dilated cardiomyopathy 1CC [RCV001059582]\|not provided [RCV000498618]	uncertain significance	1	77926604	77926604	Human	1	name
13472496	CV442888	single nucleotide variant	NM_144573.4(NEXN):c.370G>A (p.Glu124Lys)	Cardiovascular phenotype [RCV002358414]\|Dilated cardiomyopathy 1CC [RCV001312369]\|Dilated cardiomyopathy 1CC [RCV003147501]\|Hypertrophic cardiomyopathy 20 [RCV003147502]\|not provided [RCV000519143]	uncertain significance	1	77918196	77918196	Human	2	name
13502299	CV448247	single nucleotide variant	NM_144573.4(NEXN):c.871G>A (p.Glu291Lys)	Cardiovascular phenotype [RCV003380619]\|Dilated cardiomyopathy 1CC [RCV000541851]	uncertain significance	1	77929322	77929322	Human	2	name
13529633	CV509229	single nucleotide variant	NM_144573.4(NEXN):c.374G>A (p.Arg125Gln)	Cardiovascular phenotype [RCV000621766]	uncertain significance	1	77918200	77918200	Human		name
13528625	CV509230	single nucleotide variant	NM_144573.4(NEXN):c.616G>A (p.Glu206Lys)	Cardiovascular phenotype [RCV000620877]\|Dilated cardiomyopathy 1CC [RCV002531861]\|not provided [RCV001591393]	likely benign\|uncertain significance	1	77926540	77926540	Human	2	name
13527687	CV509231	single nucleotide variant	NM_144573.4(NEXN):c.620A>G (p.Asp207Gly)	Cardiomyopathy [RCV001798928]\|Cardiovascular phenotype [RCV000620155]\|Dilated cardiomyopathy 1CC [RCV001240728]\|not provided [RCV001700254]	uncertain significance	1	77926544	77926544	Human	4	name
13528374	CV509232	single nucleotide variant	NM_144573.4(NEXN):c.626G>T (p.Arg209Ile)	Cardiovascular phenotype [RCV000620700]\|Dilated cardiomyopathy 1CC [RCV001054082]	uncertain significance	1	77926550	77926550	Human	2	name
13527754	CV509234	single nucleotide variant	NM_144573.4(NEXN):c.784C>T (p.Arg262Ter)	Cardiovascular phenotype [RCV000620205]\|Dilated cardiomyopathy 1CC [RCV001223312]	conflicting interpretations of pathogenicity\|uncertain significance	1	77926812	77926812	Human	2	name
13620073	CV516083	single nucleotide variant	NM_144573.4(NEXN):c.491A>G (p.Glu164Gly)	Cardiovascular phenotype [RCV002343327]\|Dilated cardiomyopathy 1CC [RCV000647279]	uncertain significance	1	77926415	77926415	Human	2	name
13620071	CV516085	single nucleotide variant	NM_144573.4(NEXN):c.767G>A (p.Arg256Gln)	Cardiovascular phenotype [RCV004985040]\|Dilated cardiomyopathy 1CC [RCV000647278]\|not provided [RCV003441993]	uncertain significance	1	77926795	77926795	Human	2	name
13620075	CV516088	duplication	NM_144573.4(NEXN):c.1348dup (p.Ser450fs)	Dilated cardiomyopathy 1CC [RCV000647281]	pathogenic\|uncertain significance	1	77935914	77935915	Human	1	name
13620081	CV516118	single nucleotide variant	NM_144573.4(NEXN):c.818G>A (p.Arg273His)	Cardiomyopathy [RCV001798950]\|Cardiovascular phenotype [RCV002424490]\|Dilated cardiomyopathy 1CC [RCV000647285]	uncertain significance	1	77926846	77926846	Human	4	name
13813786	CV557372	single nucleotide variant	NM_144573.4(NEXN):c.643C>G (p.Gln215Glu)	Dilated cardiomyopathy 1CC [RCV000690402]\|Dilated cardiomyopathy 1CC [RCV003989583]	uncertain significance	1	77926567	77926567	Human	1	name
13822415	CV557374	single nucleotide variant	NM_144573.4(NEXN):c.752T>G (p.Phe251Cys)	Cardiovascular phenotype [RCV003163213]\|Dilated cardiomyopathy 1CC [RCV000697282]	uncertain significance	1	77926780	77926780	Human	2	name
8610773	CV57071	single nucleotide variant	NM_144573.4(NEXN):c.392A>G (p.Gln131Arg)	Cardiovascular phenotype [RCV004018910]\|Dilated cardiomyopathy 1CC [RCV001240745]\|not provided [RCV001528610]\|not specified [RCV000041178]	likely pathogenic\|uncertain significance	1	77918218	77918218	Human	2	name
8610774	CV57072	single nucleotide variant	NM_144573.4(NEXN):c.613G>A (p.Glu205Lys)	Cardiomyopathy [RCV000769815]\|Cardiovascular phenotype [RCV004018911]\|Dilated cardiomyopathy 1CC [RCV000473581]\|not provided [RCV000766514]\|not specified [RCV000041179]	uncertain significance	1	77926537	77926537	Human	4	name
8610777	CV57075	single nucleotide variant	NM_144573.4(NEXN):c.733G>A (p.Gly245Arg)	Cardiovascular phenotype [RCV000245136]\|Dilated cardiomyopathy 1CC [RCV000860033]\|not provided [RCV004713184]\|not specified [RCV000041182]	benign\|likely benign	1	77926761	77926761	Human	6	name
8610780	CV57078	single nucleotide variant	NM_144573.4(NEXN):c.893C>G (p.Thr298Arg)	Cardiomyopathy [RCV001798222]\|Cardiovascular phenotype [RCV000246908]\|Dilated cardiomyopathy 1CC [RCV000456968]\|Hypertrophic cardiomyopathy [RCV000308250]\|not provided [RCV001698953]\|not specified [RCV000041186]	benign\|likely benign\|conflicting interpretations of pathogenicity\|uncertain significance	1	77929344	77929344	Human	6	name
8610781	CV57079	single nucleotide variant	NM_144573.4(NEXN):c.995A>C (p.Glu332Ala)	Cardiomyopathy [RCV000769821]\|Cardiovascular phenotype [RCV000618713]\|Dilated cardiomyopathy 1CC [RCV000231450]\|Hypertrophic cardiomyopathy [RCV004764900]\|Premature ventricular contraction [RCV001781365]\|not provided [RCV001528784]\|not specified [RCV000041187]	benign\|likely benign\|conflicting interpretations of pathogenicity\|uncertain significance	1	77929446	77929446	Human	8	name
13838559	CV590237	single nucleotide variant	NM_144573.4(NEXN):c.799G>T (p.Glu267Ter)	Dilated cardiomyopathy 1CC [RCV000735692]\|Dilated cardiomyopathy 1CC [RCV002535432]	pathogenic\|likely pathogenic	1	77926827	77926827	Human	1	name
14393762	CV609434	single nucleotide variant	NM_144573.4(NEXN):c.906T>A (p.Phe302Leu)	Cardiomyopathy [RCV001798970]\|Cardiovascular phenotype [RCV002370005]\|Dilated cardiomyopathy 1CC [RCV001368108]\|not provided [RCV000756422]	uncertain significance	1	77929357	77929357	Human	4	name
14688364	CV614730	single nucleotide variant	NM_144573.4(NEXN):c.535T>C (p.Tyr179His)	Cardiomyopathy [RCV000768802]	uncertain significance	1	77926459	77926459	Human	2	name
14736927	CV628261	single nucleotide variant	NM_144573.4(NEXN):c.431C>T (p.Ala144Val)	Dilated cardiomyopathy 1CC [RCV000820229]	uncertain significance	1	77918257	77918257	Human	1	name
14734045	CV628262	single nucleotide variant	NM_144573.4(NEXN):c.542C>T (p.Thr181Ile)	Cardiovascular phenotype [RCV002345884]\|Dilated cardiomyopathy 1CC [RCV000818953]\|not provided [RCV001772130]	uncertain significance	1	77926466	77926466	Human	2	name
14726029	CV628263	single nucleotide variant	NM_144573.4(NEXN):c.857G>A (p.Arg286Gln)	Dilated cardiomyopathy 1CC [RCV000799051]\|Dilated cardiomyopathy 1CC [RCV002470986]	uncertain significance	1	77926885	77926885	Human	1	name
15014890	CV679369	single nucleotide variant	NM_144573.4(NEXN):c.421C>T (p.Arg141Cys)	Cardiomyopathy [RCV000852419]\|Dilated cardiomyopathy 1CC [RCV001298985]	uncertain significance	1	77918247	77918247	Human	3	name
15014891	CV679370	single nucleotide variant	NM_144573.4(NEXN):c.774A>C (p.Arg258Ser)	Hypertrophic cardiomyopathy [RCV000852420]	uncertain significance	1	77926802	77926802	Human	2	name
28912203	CV682593	single nucleotide variant	NM_144573.4(NEXN):c.826G>A (p.Glu276Lys)	Hypertrophic cardiomyopathy [RCV001093542]	likely pathogenic\|likely benign	1	77926854	77926854	Human	2	name
21071593	CV794724	single nucleotide variant	NM_144573.4(NEXN):c.380G>A (p.Arg127His)	Cardiomyopathy [RCV001799019]\|Cardiovascular phenotype [RCV004030163]\|Dilated cardiomyopathy 1CC [RCV001858780]\|not provided [RCV000994028]	likely benign\|uncertain significance	1	77918206	77918206	Human	4	name
26921602	CV824422	single nucleotide variant	NM_144573.4(NEXN):c.848A>T (p.Glu283Val)	Cardiovascular phenotype [RCV003307896]\|Dilated cardiomyopathy 1CC [RCV001061139]\|not provided [RCV001553325]	uncertain significance	1	77926876	77926876	Human	2	name
28893590	CV903740	single nucleotide variant	NM_144573.4(NEXN):c.373C>T (p.Arg125Ter)	Cardiomyopathy [RCV001170497]\|Dilated cardiomyopathy 1CC [RCV005225255]	pathogenic\|uncertain significance	1	77918199	77918199	Human	3	name
38479319	CV930662	single nucleotide variant	NM_144573.4(NEXN):c.749C>G (p.Thr250Ser)	Dilated cardiomyopathy 1CC [RCV001205924]	uncertain significance	1	77926777	77926777	Human	1	name
38468351	CV930663	single nucleotide variant	NM_144573.4(NEXN):c.910G>C (p.Gly304Arg)	Dilated cardiomyopathy 1CC [RCV001213123]	uncertain significance	1	77929361	77929361	Human	1	name
39456224	CV966408	single nucleotide variant	NM_144573.4(NEXN):c.460A>G (p.Asn154Asp)	Dilated cardiomyopathy 1A [RCV001256886]	uncertain significance	1	77925200	77925200	Human	2	name
39456221	CV966409	single nucleotide variant	NM_144573.4(NEXN):c.917G>A (p.Arg306His)	Cardiomyopathy [RCV003150414]\|Cardiovascular phenotype [RCV002375314]\|Dilated cardiomyopathy 1CC [RCV002570613]\|Hypertrophic cardiomyopathy 1 [RCV001256883]	uncertain significance	1	77929368	77929368	Human	5	name
40814914	CV970701	single nucleotide variant	NM_144573.4(NEXN):c.633A>T (p.Arg211Ser)	Dilated cardiomyopathy 1CC [RCV001262354]	uncertain significance	1	77926557	77926557	Human	1	name
126765899	CV987752	single nucleotide variant	NM_144573.4(NEXN):c.335A>G (p.Gln112Arg)	Dilated cardiomyopathy 1CC [RCV001301670]	uncertain significance	1	77918161	77918161	Human	1	name
126734951	CV987753	single nucleotide variant	NM_144573.4(NEXN):c.793C>A (p.Gln265Lys)	Cardiovascular phenotype [RCV004036316]\|Dilated cardiomyopathy 1CC [RCV001304527]	uncertain significance	1	77926821	77926821	Human	2	name
126751391	CV987754	single nucleotide variant	NM_144573.4(NEXN):c.794A>C (p.Gln265Pro)	Cardiovascular phenotype [RCV002418931]\|Dilated cardiomyopathy 1CC [RCV001307029]	uncertain significance	1	77926822	77926822	Human	2	name
126759465	CV1003007	single nucleotide variant	NM_144573.4(NEXN):c.1498G>T (p.Ala500Ser)	Cardiovascular phenotype [RCV003294275]\|Dilated cardiomyopathy 1CC [RCV001318065]	uncertain significance	1	77942047	77942047	Human	2	name
126763190	CV1003012	single nucleotide variant	NM_144573.4(NEXN):c.2017A>G (p.Ser673Gly)	Dilated cardiomyopathy 1CC [RCV001319151]	uncertain significance	1	77942818	77942818	Human	1	name
126736783	CV1015791	single nucleotide variant	NM_144573.4(NEXN):c.1640T>A (p.Ile547Asn)	Dilated cardiomyopathy 1CC [RCV001328613]\|Dilated cardiomyopathy 1CC [RCV002493718]	uncertain significance	1	77942189	77942189	Human	1	name
126734992	CV1023495	single nucleotide variant	NM_144573.4(NEXN):c.1066G>C (p.Asp356His)	Dilated cardiomyopathy 1CC [RCV001350030]	uncertain significance	1	77933294	77933294	Human	1	name
126761664	CV1023496	single nucleotide variant	NM_144573.4(NEXN):c.1072C>T (p.Pro358Ser)	Cardiovascular phenotype [RCV005372656]\|Dilated cardiomyopathy 1CC [RCV001340755]	uncertain significance	1	77933300	77933300	Human	2	name
126726064	CV1023497	single nucleotide variant	NM_144573.4(NEXN):c.1660A>G (p.Lys554Glu)	Dilated cardiomyopathy 1CC [RCV001348346]	uncertain significance	1	77942461	77942461	Human	1	name
126772856	CV1023498	single nucleotide variant	NM_144573.4(NEXN):c.1724A>G (p.Glu575Gly)	Dilated cardiomyopathy 1CC [RCV001345859]\|not provided [RCV003886503]	uncertain significance	1	77942525	77942525	Human	1	name
126774904	CV1023499	single nucleotide variant	NM_144573.4(NEXN):c.1951G>A (p.Glu651Lys)	Cardiovascular phenotype [RCV004988574]\|Dilated cardiomyopathy 1CC [RCV001347761]	uncertain significance	1	77942752	77942752	Human	2	name
126910963	CV1040326	single nucleotide variant	NM_144573.4(NEXN):c.1322G>A (p.Gly441Asp)	Dilated cardiomyopathy 1CC [RCV001368992]	uncertain significance	1	77935893	77935893	Human	1	name
126915945	CV1040327	single nucleotide variant	NM_144573.4(NEXN):c.1661A>G (p.Lys554Arg)	Dilated cardiomyopathy 1CC [RCV001360282]	uncertain significance	1	77942462	77942462	Human	1	name
150334165	CV1164100	single nucleotide variant	NM_144573.4(NEXN):c.1364T>C (p.Ile455Thr)	Cardiomyopathy [RCV001799098]\|not provided [RCV001529351]	uncertain significance	1	77935935	77935935	Human	2	name
150486475	CV1274347	single nucleotide variant	NM_144573.4(NEXN):c.1749G>A (p.Trp583Ter)	not provided [RCV001698937]	uncertain significance	1	77942550	77942550	Human		name
150520698	CV1289860	single nucleotide variant	NM_144573.4(NEXN):c.1733G>T (p.Arg578Ile)	not provided [RCV001730232]	uncertain significance	1	77942534	77942534	Human		name
150520926	CV1289991	single nucleotide variant	NM_144573.4(NEXN):c.1810A>G (p.Lys604Glu)	not provided [RCV001730380]	uncertain significance	1	77942611	77942611	Human		name
150551111	CV1292508	single nucleotide variant	NM_144573.4(NEXN):c.1143A>T (p.Leu381Phe)	not provided [RCV001754115]	uncertain significance	1	77933371	77933371	Human		name
150548648	CV1294432	single nucleotide variant	NM_144573.4(NEXN):c.1498G>A (p.Ala500Thr)	not provided [RCV001751924]	uncertain significance	1	77942047	77942047	Human		name
150555302	CV1297745	single nucleotide variant	NM_144573.4(NEXN):c.1802T>G (p.Phe601Cys)	not provided [RCV001772652]	uncertain significance	1	77942603	77942603	Human		name
151232923	CV1320021	single nucleotide variant	NM_144573.4(NEXN):c.1720G>A (p.Glu574Lys)	Cardiomyopathy [RCV001799377]\|Cardiovascular phenotype [RCV003163935]	uncertain significance	1	77942521	77942521	Human	2	name
151232929	CV1320024	single nucleotide variant	NM_144573.4(NEXN):c.2019T>A (p.Ser673Arg)	Cardiomyopathy [RCV001799380]\|Cardiovascular phenotype [RCV002422858]\|Dilated cardiomyopathy 1CC [RCV001868908]	uncertain significance	1	77942820	77942820	Human	4	name
151808453	CV1362768	single nucleotide variant	NM_144573.4(NEXN):c.1889A>G (p.Tyr630Cys)	Cardiovascular phenotype [RCV002407261]\|Dilated cardiomyopathy 1CC [RCV001991596]	uncertain significance	1	77942690	77942690	Human	2	name
151857751	CV1363908	single nucleotide variant	NM_144573.4(NEXN):c.1943A>G (p.Asp648Gly)	Dilated cardiomyopathy 1CC [RCV001904900]	uncertain significance	1	77942744	77942744	Human	1	name
151860709	CV1374102	single nucleotide variant	NM_144573.4(NEXN):c.1747T>C (p.Trp583Arg)	Cardiovascular phenotype [RCV002397914]\|Dilated cardiomyopathy 1CC [RCV001938504]	uncertain significance	1	77942548	77942548	Human	2	name
151821253	CV1378536	single nucleotide variant	NM_144573.4(NEXN):c.1175G>C (p.Arg392Pro)	Dilated cardiomyopathy 1CC [RCV002029913]	uncertain significance	1	77933403	77933403	Human	1	name
151748984	CV1380804	single nucleotide variant	NM_144573.4(NEXN):c.1678G>A (p.Glu560Lys)	Cardiovascular phenotype [RCV004046756]\|Dilated cardiomyopathy 1CC [RCV002023173]	uncertain significance	1	77942479	77942479	Human	2	name
151771076	CV1404352	single nucleotide variant	NM_144573.4(NEXN):c.1321G>T (p.Gly441Cys)	Dilated cardiomyopathy 1CC [RCV002045249]	uncertain significance	1	77935892	77935892	Human	1	name
151821881	CV1418613	single nucleotide variant	NM_144573.4(NEXN):c.1508G>A (p.Ser503Asn)	Cardiovascular phenotype [RCV002388855]\|Dilated cardiomyopathy 1CC [RCV001954835]	uncertain significance	1	77942057	77942057	Human	2	name
151775434	CV1420028	single nucleotide variant	NM_144573.4(NEXN):c.1422G>C (p.Arg474Ser)	Dilated cardiomyopathy 1CC [RCV001988645]	uncertain significance	1	77935993	77935993	Human	1	name
8692248	CV142214	single nucleotide variant	NM_144573.4(NEXN):c.1408G>C (p.Glu470Gln)	Cardiomyopathy [RCV001170729]\|Cardiovascular phenotype [RCV000245536]\|Dilated cardiomyopathy 1CC [RCV000204884]\|not provided [RCV004713338]\|not specified [RCV000154659]	benign\|uncertain significance	1	77935979	77935979	Human	4	name
151749497	CV1430337	single nucleotide variant	NM_144573.4(NEXN):c.1412G>A (p.Arg471Gln)	Dilated cardiomyopathy 1CC [RCV002006714]	uncertain significance	1	77935983	77935983	Human	1	name
151794798	CV1434336	single nucleotide variant	NM_144573.4(NEXN):c.1057G>A (p.Val353Ile)	Dilated cardiomyopathy 1CC [RCV001866579]	uncertain significance	1	77933285	77933285	Human	1	name
151785495	CV1435352	single nucleotide variant	NM_144573.4(NEXN):c.1226A>C (p.Glu409Ala)	Dilated cardiomyopathy 1CC [RCV001916274]	uncertain significance	1	77933454	77933454	Human	1	name
151821372	CV1443346	single nucleotide variant	NM_144573.4(NEXN):c.1195C>A (p.His399Asn)	Cardiovascular phenotype [RCV004988783]\|Dilated cardiomyopathy 1CC [RCV002049834]	uncertain significance	1	77933423	77933423	Human	2	name
151883896	CV1452507	single nucleotide variant	NM_144573.4(NEXN):c.1835A>G (p.Glu612Gly)	Dilated cardiomyopathy 1CC [RCV002037439]	uncertain significance	1	77942636	77942636	Human	1	name
151751941	CV1459082	single nucleotide variant	NM_144573.4(NEXN):c.1957A>G (p.Met653Val)	Cardiovascular phenotype [RCV002423258]\|Dilated cardiomyopathy 1CC [RCV002043373]	uncertain significance	1	77942758	77942758	Human	2	name
8555558	CV15365	single nucleotide variant	NM_144573.4(NEXN):c.1955A>G (p.Tyr652Cys)	Cardiomyopathy [RCV001170736]\|Cardiovascular phenotype [RCV000246924]\|Dilated cardiomyopathy 1CC [RCV000000354]\|Dilated cardiomyopathy 1CC [RCV000234084]\|Dilated cardiomyopathy 1S [RCV000491470]\|Hypertrophic cardiomyopathy 20 [RCV003147270]\|Primary dilated cardiomyopathy [RCV000208290]\|not provided ... (more) [RCV000183674]\|not specified [RCV005406714]	pathogenic\|likely pathogenic\|conflicting interpretations of pathogenicity\|uncertain significance	1	77942756	77942756	Human	6	name
8555559	CV15366	single nucleotide variant	NM_144573.4(NEXN):c.1831C>A (p.Pro611Thr)	Cardiovascular phenotype [RCV004018524]\|Dilated cardiomyopathy 1CC [RCV000000355]	pathogenic\|uncertain significance	1	77942632	77942632	Human	1	name
152034171	CV1669465	single nucleotide variant	NM_144573.4(NEXN):c.1411C>T (p.Arg471Ter)	Cardiovascular phenotype [RCV002391371]\|Dilated cardiomyopathy 1CC [RCV005213622]\|not provided [RCV002223456]	pathogenic\|uncertain significance	1	77935982	77935982	Human	2	name
152999853	CV1683400	single nucleotide variant	NM_144573.4(NEXN):c.1450C>T (p.Arg484Ter)	Dilated cardiomyopathy 1CC [RCV002502058]\|See cases [RCV002252584]	conflicting interpretations of pathogenicity\|uncertain significance	1	77936021	77936021	Human	1	name
153303611	CV1686381	single nucleotide variant	NM_144573.4(NEXN):c.1192A>C (p.Lys398Gln)	not provided [RCV002261814]	uncertain significance	1	77933420	77933420	Human		name
153302322	CV1688172	single nucleotide variant	NM_144573.4(NEXN):c.1232T>A (p.Leu411Gln)	not provided [RCV002265398]	uncertain significance	1	77933460	77933460	Human		name
153303688	CV1690420	single nucleotide variant	NM_144573.4(NEXN):c.1469A>G (p.His490Arg)	Cardiovascular phenotype [RCV004982962]\|not provided [RCV002269464]	uncertain significance	1	77936040	77936040	Human		name
153345821	CV1691454	single nucleotide variant	NM_144573.4(NEXN):c.1499C>A (p.Ala500Glu)	Cardiomyopathy [RCV002272937]	uncertain significance	1	77942048	77942048	Human	2	name
155267014	CV1696454	single nucleotide variant	NM_144573.4(NEXN):c.1850T>G (p.Phe617Cys)	not provided [RCV002281312]	uncertain significance	1	77942651	77942651	Human		name
9690249	CV172601	single nucleotide variant	NM_144573.4(NEXN):c.1430T>G (p.Ile477Ser)	Cardiovascular phenotype [RCV002390360]\|not specified [RCV000155922]	uncertain significance	1	77936001	77936001	Human		name
9690388	CV172602	single nucleotide variant	NM_144573.4(NEXN):c.1528A>G (p.Lys510Glu)	Cardiovascular phenotype [RCV002390363]\|Dilated cardiomyopathy 1CC [RCV001051771]\|not provided [RCV003441759]\|not specified [RCV000156066]	uncertain significance	1	77942077	77942077	Human	2	name
9832459	CV178469	single nucleotide variant	NM_144573.4(NEXN):c.1582G>C (p.Glu528Gln)	Cardiomyopathy [RCV001170732]\|Cardiovascular phenotype [RCV002399564]\|Dilated cardiomyopathy 1CC [RCV000470637]\|NEXN-related disorder [RCV004535025]\|not provided [RCV001719988]\|not specified [RCV000157390]	likely benign\|uncertain significance	1	77942131	77942131	Human	4	name , trait , alternate_id
155741845	CV1791157	single nucleotide variant	NM_144573.4(NEXN):c.1014G>C (p.Glu338Asp)	Cardiovascular phenotype [RCV002333543]	uncertain significance	1	77929465	77929465	Human		name
155704149	CV1798066	single nucleotide variant	NM_144573.4(NEXN):c.1175G>T (p.Arg392Leu)	Cardiovascular phenotype [RCV002333983]	uncertain significance	1	77933403	77933403	Human		name
155668616	CV1799934	single nucleotide variant	NM_144573.4(NEXN):c.1201C>G (p.Leu401Val)	Cardiovascular phenotype [RCV002349688]	uncertain significance	1	77933429	77933429	Human		name
155732857	CV1801913	single nucleotide variant	NM_144573.4(NEXN):c.1186G>A (p.Glu396Lys)	Cardiovascular phenotype [RCV002340277]	uncertain significance	1	77933414	77933414	Human		name
155708952	CV1808811	single nucleotide variant	NM_144573.4(NEXN):c.1015G>A (p.Glu339Lys)	Cardiovascular phenotype [RCV002335478]	uncertain significance	1	77929466	77929466	Human		name
155729174	CV1823471	single nucleotide variant	NM_144573.4(NEXN):c.1249G>A (p.Glu417Lys)	Cardiovascular phenotype [RCV002400611]\|not provided [RCV002508357]	uncertain significance	1	77933477	77933477	Human		name
155731576	CV1825986	single nucleotide variant	NM_144573.4(NEXN):c.1024A>G (p.Lys342Glu)	Cardiovascular phenotype [RCV002383203]	uncertain significance	1	77929475	77929475	Human		name
155700594	CV1828470	single nucleotide variant	NM_144573.4(NEXN):c.1744C>T (p.Pro582Ser)	Cardiovascular phenotype [RCV002401454]	uncertain significance	1	77942545	77942545	Human		name
155681684	CV1829725	single nucleotide variant	NM_144573.4(NEXN):c.1407A>C (p.Glu469Asp)	Cardiovascular phenotype [RCV002389390]	uncertain significance	1	77935978	77935978	Human		name
155688598	CV1829964	single nucleotide variant	NM_144573.4(NEXN):c.1417A>G (p.Arg473Gly)	Cardiovascular phenotype [RCV002391715]	uncertain significance	1	77935988	77935988	Human		name
155714242	CV1830148	single nucleotide variant	NM_144573.4(NEXN):c.1484T>C (p.Val495Ala)	Cardiovascular phenotype [RCV002397216]\|not specified [RCV005405911]	likely benign\|uncertain significance	1	77942033	77942033	Human		name
155719671	CV1830615	single nucleotide variant	NM_144573.4(NEXN):c.1568C>T (p.Ala523Val)	Cardiovascular phenotype [RCV002405571]\|Dilated cardiomyopathy 1CC [RCV003096946]	uncertain significance	1	77942117	77942117	Human	2	name
155710738	CV1831117	single nucleotide variant	NM_144573.4(NEXN):c.1051A>G (p.Met351Val)	Cardiovascular phenotype [RCV002403634]	uncertain significance	1	77929502	77929502	Human		name
155711132	CV1831176	single nucleotide variant	NM_144573.4(NEXN):c.1652T>C (p.Leu551Pro)	Cardiovascular phenotype [RCV002403682]	uncertain significance	1	77942201	77942201	Human		name
155738361	CV1832018	single nucleotide variant	NM_144573.4(NEXN):c.1819G>A (p.Gly607Arg)	Cardiovascular phenotype [RCV002410316]	uncertain significance	1	77942620	77942620	Human		name
155670137	CV1832280	single nucleotide variant	NM_144573.4(NEXN):c.1316G>A (p.Arg439Lys)	Cardiovascular phenotype [RCV002385578]	uncertain significance	1	77935887	77935887	Human		name
155708833	CV1832567	single nucleotide variant	NM_144573.4(NEXN):c.1385A>T (p.Glu462Val)	Cardiovascular phenotype [RCV002396505]	uncertain significance	1	77935956	77935956	Human		name
155709934	CV1832738	single nucleotide variant	NM_144573.4(NEXN):c.1390C>T (p.Gln464Ter)	Cardiovascular phenotype [RCV002396676]	uncertain significance	1	77935961	77935961	Human		name
155733016	CV1834173	single nucleotide variant	NM_144573.4(NEXN):c.1634G>C (p.Arg545Thr)	Cardiovascular phenotype [RCV002401347]	uncertain significance	1	77942183	77942183	Human		name
155731586	CV1834854	single nucleotide variant	NM_144573.4(NEXN):c.1789G>A (p.Glu597Lys)	Cardiovascular phenotype [RCV002407750]\|Dilated cardiomyopathy 1CC [RCV003100843]	uncertain significance	1	77942590	77942590	Human	2	name
155731813	CV1834973	single nucleotide variant	NM_144573.4(NEXN):c.1796T>G (p.Val599Gly)	Cardiovascular phenotype [RCV002407803]	uncertain significance	1	77942597	77942597	Human		name
155719667	CV1835664	single nucleotide variant	NM_144573.4(NEXN):c.1025A>C (p.Lys342Thr)	Cardiovascular phenotype [RCV002380665]	uncertain significance	1	77929476	77929476	Human		name
155734107	CV1836274	single nucleotide variant	NM_144573.4(NEXN):c.1030T>G (p.Phe344Val)	Cardiovascular phenotype [RCV002383793]\|Dilated cardiomyopathy 1CC [RCV003774292]	uncertain significance	1	77929481	77929481	Human	2	name
155706858	CV1837269	single nucleotide variant	NM_144573.4(NEXN):c.1537A>G (p.Met513Val)	Cardiovascular phenotype [RCV002403057]	uncertain significance	1	77942086	77942086	Human		name
155720107	CV1837463	single nucleotide variant	NM_144573.4(NEXN):c.1604A>G (p.Gln535Arg)	Cardiovascular phenotype [RCV002398750]	uncertain significance	1	77942153	77942153	Human		name
155703748	CV1838502	single nucleotide variant	NM_144573.4(NEXN):c.1774T>A (p.Ser592Thr)	Cardiovascular phenotype [RCV002401867]	uncertain significance	1	77942575	77942575	Human		name
155730606	CV1839053	single nucleotide variant	NM_144573.4(NEXN):c.1757A>G (p.Lys586Arg)	Cardiovascular phenotype [RCV002407565]	uncertain significance	1	77942558	77942558	Human		name
155738742	CV1839115	single nucleotide variant	NM_144573.4(NEXN):c.1826C>G (p.Pro609Arg)	Cardiovascular phenotype [RCV002410439]	uncertain significance	1	77942627	77942627	Human		name
155743624	CV1839491	single nucleotide variant	NM_144573.4(NEXN):c.1064A>G (p.Asp355Gly)	Cardiovascular phenotype [RCV002412910]	uncertain significance	1	77933292	77933292	Human		name
155682493	CV1839802	single nucleotide variant	NM_144573.4(NEXN):c.1976A>G (p.Asn659Ser)	Cardiovascular phenotype [RCV002423578]	uncertain significance	1	77942777	77942777	Human		name
155675131	CV1843217	single nucleotide variant	NM_144573.4(NEXN):c.1070C>T (p.Ser357Phe)	Cardiovascular phenotype [RCV002421581]\|not provided [RCV004721065]	uncertain significance	1	77933298	77933298	Human		name
155675725	CV1843304	single nucleotide variant	NM_144573.4(NEXN):c.1958T>C (p.Met653Thr)	Cardiovascular phenotype [RCV002421668]	uncertain significance	1	77942759	77942759	Human		name
155739745	CV1846078	single nucleotide variant	NM_144573.4(NEXN):c.1922T>G (p.Leu641Ter)	Cardiovascular phenotype [RCV002410746]	uncertain significance	1	77942723	77942723	Human		name
155683795	CV1853601	single nucleotide variant	NM_144573.4(NEXN):c.1121T>G (p.Leu374Arg)	Cardiovascular phenotype [RCV002440232]	uncertain significance	1	77933349	77933349	Human		name
156059961	CV1876215	single nucleotide variant	NM_144573.4(NEXN):c.1659G>C (p.Lys553Asn)	Dilated cardiomyopathy 1CC [RCV003053306]	uncertain significance	1	77942208	77942208	Human	1	name
156327428	CV1887380	single nucleotide variant	NM_144573.4(NEXN):c.1084A>C (p.Lys362Gln)	Dilated cardiomyopathy 1CC [RCV003089577]	uncertain significance	1	77933312	77933312	Human	1	name
156367100	CV1908611	single nucleotide variant	NM_144573.4(NEXN):c.1112C>A (p.Pro371Gln)	Dilated cardiomyopathy 1CC [RCV002582140]	uncertain significance	1	77933340	77933340	Human	1	name
156017298	CV1918451	single nucleotide variant	NM_144573.4(NEXN):c.1162G>A (p.Glu388Lys)	Cardiovascular phenotype [RCV003384343]\|Dilated cardiomyopathy 1CC [RCV002636532]	uncertain significance	1	77933390	77933390	Human	2	name
156156464	CV1957822	single nucleotide variant	NM_144573.4(NEXN):c.1242A>C (p.Glu414Asp)	Cardiovascular phenotype [RCV005405931]\|Dilated cardiomyopathy 1CC [RCV002573072]	uncertain significance	1	77933470	77933470	Human	2	name
10055891	CV198085	single nucleotide variant	NM_144573.4(NEXN):c.1010T>C (p.Ile337Thr)	Cardiovascular phenotype [RCV002321736]\|Dilated cardiomyopathy 1CC [RCV001852363]\|not provided [RCV000183655]	uncertain significance	1	77929461	77929461	Human	2	name
10055892	CV198086	single nucleotide variant	NM_144573.4(NEXN):c.1028C>T (p.Ala343Val)	Cardiovascular phenotype [RCV002381606]\|not provided [RCV000183656]	uncertain significance	1	77929479	77929479	Human		name
10055893	CV198087	single nucleotide variant	NM_144573.4(NEXN):c.1094C>G (p.Ser365Cys)	not provided [RCV000183658]	uncertain significance	1	77933322	77933322	Human		name
10055894	CV198088	single nucleotide variant	NM_144573.4(NEXN):c.1222T>C (p.Phe408Leu)	Cardiovascular phenotype [RCV002361182]\|Dilated cardiomyopathy 1CC [RCV001896505]	uncertain significance	1	77933450	77933450	Human	2	name
10055895	CV198089	single nucleotide variant	NM_144573.4(NEXN):c.1271C>T (p.Thr424Ile)	Cardiomyopathy [RCV001170728]\|Cardiovascular phenotype [RCV002372124]\|Dilated cardiomyopathy 1A [RCV001256887]\|Dilated cardiomyopathy 1CC [RCV000529099]\|not provided [RCV000183662]	uncertain significance	1	77935842	77935842	Human	7	name
10055905	CV198091	single nucleotide variant	NM_144573.4(NEXN):c.1430T>C (p.Ile477Thr)	Cardiomyopathy [RCV000769824]\|Cardiovascular phenotype [RCV002390473]\|Dilated cardiomyopathy 1CC [RCV000701167]	uncertain significance	1	77936001	77936001	Human	4	name
10055896	CV198092	single nucleotide variant	NM_144573.4(NEXN):c.1435C>T (p.Leu479Phe)	Cardiovascular phenotype [RCV000619532]\|Dilated cardiomyopathy 1CC [RCV000535150]\|Primary familial hypertrophic cardiomyopathy [RCV000845501]\|not provided [RCV000766517]\|not specified [RCV000223852]	uncertain significance	1	77936006	77936006	Human	4	name
10055897	CV198094	single nucleotide variant	NM_144573.4(NEXN):c.1471G>C (p.Glu491Gln)	Cardiovascular phenotype [RCV002390472]\|Dilated cardiomyopathy 1CC [RCV000647280]\|not provided [RCV000183664]	uncertain significance	1	77936042	77936042	Human	2	name
10055898	CV198095	single nucleotide variant	NM_144573.4(NEXN):c.1565A>C (p.Lys522Thr)	Cardiovascular phenotype [RCV004524747]	uncertain significance	1	77942114	77942114	Human		name
10055914	CV198096	single nucleotide variant	NM_144573.4(NEXN):c.1595T>C (p.Ile532Thr)	Cardiovascular phenotype [RCV002399678]\|Dilated cardiomyopathy 1CC [RCV001360627]\|Hypertrophic cardiomyopathy 1 [RCV001256888]\|not provided [RCV000183685]	uncertain significance	1	77942144	77942144	Human	3	name
10055899	CV198097	single nucleotide variant	NM_144573.4(NEXN):c.1615C>T (p.Arg539Cys)	Cardiovascular phenotype [RCV002399676]\|Dilated cardiomyopathy 1CC [RCV001852364]\|not provided [RCV000183666]	uncertain significance	1	77942164	77942164	Human	2	name
10055900	CV198098	single nucleotide variant	NM_144573.4(NEXN):c.1618A>G (p.Met540Val)	Cardiomyopathy [RCV001170733]\|Cardiovascular phenotype [RCV000618620]\|Dilated cardiomyopathy 1CC [RCV000547608]\|not provided [RCV001711351]\|not specified [RCV000213635]	benign\|likely benign\|conflicting interpretations of pathogenicity\|uncertain significance	1	77942167	77942167	Human	4	name
10055915	CV198099	single nucleotide variant	NM_144573.4(NEXN):c.1640T>C (p.Ile547Thr)	Cardiovascular phenotype [RCV000618647]\|Dilated cardiomyopathy 1CC [RCV000820361]\|not provided [RCV000183686]	uncertain significance	1	77942189	77942189	Human	2	name
10055901	CV198101	single nucleotide variant	NM_144573.4(NEXN):c.1684G>C (p.Glu562Gln)	not provided [RCV000183668]	uncertain significance	1	77942485	77942485	Human		name
10055902	CV198102	single nucleotide variant	NM_144573.4(NEXN):c.1733G>C (p.Arg578Thr)	Cardiovascular phenotype [RCV002399677]\|not provided [RCV000183669]	uncertain significance	1	77942534	77942534	Human		name
10055903	CV198103	single nucleotide variant	NM_144573.4(NEXN):c.1805C>T (p.Thr602Met)	Cardiovascular phenotype [RCV002408809]\|Dilated cardiomyopathy 1CC [RCV002503720]\|not provided [RCV000183670]\|not specified [RCV003488437]	likely pathogenic\|uncertain significance	1	77942606	77942606	Human	2	name
10055904	CV198104	single nucleotide variant	NM_144573.4(NEXN):c.1911C>A (p.Tyr637Ter)	Dilated cardiomyopathy 1CC [RCV001309065]\|not provided [RCV000183671]	uncertain significance	1	77942712	77942712	Human	1	name
10055906	CV198105	single nucleotide variant	NM_144573.4(NEXN):c.1935C>G (p.Phe645Leu)	not provided [RCV000183673]\|not specified [RCV000223684]	likely pathogenic\|uncertain significance	1	77942736	77942736	Human		name
10055907	CV198106	single nucleotide variant	NM_144573.4(NEXN):c.2000G>A (p.Cys667Tyr)	Cardiovascular phenotype [RCV004649087]\|not provided [RCV000183675]	likely pathogenic\|uncertain significance	1	77942801	77942801	Human		name
155913899	CV1990321	single nucleotide variant	NM_144573.4(NEXN):c.1012G>C (p.Glu338Gln)	Dilated cardiomyopathy 1CC [RCV002614187]	uncertain significance	1	77929463	77929463	Human	1	name
156191788	CV2017034	single nucleotide variant	NM_144573.4(NEXN):c.1374G>T (p.Leu458Phe)	Dilated cardiomyopathy 1CC [RCV002711112]	uncertain significance	1	77935945	77935945	Human	1	name
156129566	CV2037343	single nucleotide variant	NM_144573.4(NEXN):c.1829A>G (p.Lys610Arg)	Dilated cardiomyopathy 1CC [RCV002800559]	uncertain significance	1	77942630	77942630	Human	1	name
156083079	CV2060258	single nucleotide variant	NM_144573.4(NEXN):c.1886A>G (p.Gln629Arg)	Dilated cardiomyopathy 1CC [RCV002823919]	uncertain significance	1	77942687	77942687	Human	1	name
156171698	CV2075602	single nucleotide variant	NM_144573.4(NEXN):c.1867C>G (p.Gln623Glu)	Dilated cardiomyopathy 1CC [RCV002851551]	uncertain significance	1	77942668	77942668	Human	1	name
155902452	CV2083914	single nucleotide variant	NM_144573.4(NEXN):c.1049A>G (p.Asn350Ser)	Dilated cardiomyopathy 1CC [RCV002857945]	uncertain significance	1	77929500	77929500	Human	1	name
156293949	CV2111553	single nucleotide variant	NM_144573.4(NEXN):c.1525C>A (p.His509Asn)	Dilated cardiomyopathy 1CC [RCV002922267]	uncertain significance	1	77942074	77942074	Human	1	name
155977590	CV2132508	single nucleotide variant	NM_144573.4(NEXN):c.1088C>T (p.Thr363Ile)	Dilated cardiomyopathy 1CC [RCV002995933]	uncertain significance	1	77933316	77933316	Human	1	name
156331808	CV2181119	single nucleotide variant	NM_144573.4(NEXN):c.1501A>T (p.Arg501Ter)	Dilated cardiomyopathy 1CC [RCV003047262]	pathogenic	1	77942050	77942050	Human	1	name
156028619	CV2185797	single nucleotide variant	NM_144573.4(NEXN):c.1959G>A (p.Met653Ile)	Cardiovascular phenotype [RCV004983281]\|Dilated cardiomyopathy 1CC [RCV003036085]	uncertain significance	1	77942760	77942760	Human	2	name
156137894	CV2186591	single nucleotide variant	NM_144573.4(NEXN):c.1084A>T (p.Lys362Ter)	Dilated cardiomyopathy 1CC [RCV003056070]	pathogenic	1	77933312	77933312	Human	1	name
11039953	CV224216	single nucleotide variant	NM_144573.4(NEXN):c.1400T>C (p.Ile467Thr)	Cardiovascular phenotype [RCV000248087]\|Primary familial hypertrophic cardiomyopathy [RCV000208073]	uncertain significance	1	77935971	77935971	Human	2	name
155947938	CV2245809	single nucleotide variant	NM_144573.4(NEXN):c.1169A>C (p.Lys390Thr)	Cardiovascular phenotype [RCV004111664]	uncertain significance	1	77933397	77933397	Human		name
156242433	CV2246221	single nucleotide variant	NM_144573.4(NEXN):c.1694T>C (p.Ile565Thr)	Cardiovascular phenotype [RCV004107681]	uncertain significance	1	77942495	77942495	Human		name
155919186	CV2279372	single nucleotide variant	NM_144573.4(NEXN):c.1549T>G (p.Phe517Val)	Cardiovascular phenotype [RCV004141926]	uncertain significance	1	77942098	77942098	Human		name
11095749	CV228518	single nucleotide variant	NM_144573.4(NEXN):c.1174C>T (p.Arg392Ter)	Cardiovascular phenotype [RCV002327090]\|Dilated cardiomyopathy 1CC [RCV000820993]\|Dilated cardiomyopathy 1CC [RCV001196151]\|Hypertrophic cardiomyopathy [RCV001375648]\|Primary dilated cardiomyopathy [RCV003993895]\|not provided [RCV001357462]\|not specified [RCV000222720]	likely pathogenic\|conflicting interpretations of pathogenicity\|uncertain significance	1	77933402	77933402	Human	5	name
11089656	CV228519	single nucleotide variant	NM_144573.4(NEXN):c.1190G>A (p.Arg397Gln)	Cardiomyopathy [RCV000769823]\|Cardiovascular phenotype [RCV002338685]\|Dilated cardiomyopathy 1CC [RCV001853472]\|not provided [RCV002288842]\|not specified [RCV000215086]	uncertain significance	1	77933418	77933418	Human	4	name
11093144	CV228520	single nucleotide variant	NM_144573.4(NEXN):c.1234A>G (p.Arg412Gly)	Cardiomyopathy [RCV001798706]\|Cardiovascular phenotype [RCV003165543]\|not specified [RCV000219409]	uncertain significance	1	77933462	77933462	Human	2	name
11095961	CV228521	single nucleotide variant	NM_144573.4(NEXN):c.1415C>G (p.Ala472Gly)	Cardiovascular phenotype [RCV002390583]\|Dilated cardiomyopathy 1CC [RCV000466479]\|not provided [RCV004791333]\|not specified [RCV000222980]	uncertain significance	1	77935986	77935986	Human	2	name
11095678	CV228523	single nucleotide variant	NM_144573.4(NEXN):c.1981G>A (p.Gly661Arg)	Cardiomyopathy [RCV000768811]\|Cardiovascular phenotype [RCV002415903]\|Dilated cardiomyopathy 1CC [RCV001359679]\|not provided [RCV005235138]\|not specified [RCV000222628]	uncertain significance	1	77942782	77942782	Human	4	name
11090621	CV228524	single nucleotide variant	NM_144573.4(NEXN):c.2015A>G (p.Glu672Gly)	Cardiovascular phenotype [RCV005372267]\|not specified [RCV000216284]	uncertain significance	1	77942816	77942816	Human		name
156292156	CV2296766	single nucleotide variant	NM_144573.4(NEXN):c.1772C>T (p.Thr591Ile)	Cardiovascular phenotype [RCV004148666]	uncertain significance	1	77942573	77942573	Human		name
243055966	CV2416714	single nucleotide variant	NM_144573.4(NEXN):c.1271C>A (p.Thr424Asn)	Cardiomyopathy [RCV003150799]	uncertain significance	1	77935842	77935842	Human	2	name
243055968	CV2416716	single nucleotide variant	NM_144573.4(NEXN):c.1678G>C (p.Glu560Gln)	Cardiomyopathy [RCV003150801]	uncertain significance	1	77942479	77942479	Human	2	name
329368688	CV2426302	single nucleotide variant	NM_144573.4(NEXN):c.1867C>T (p.Gln623Ter)	Cardiovascular phenotype [RCV003171388]\|not provided [RCV004697274]	uncertain significance	1	77942668	77942668	Human		name
329378793	CV2432748	single nucleotide variant	NM_144573.4(NEXN):c.1510G>A (p.Glu504Lys)	Cardiovascular phenotype [RCV003186934]	uncertain significance	1	77942059	77942059	Human		name
329378797	CV2432751	single nucleotide variant	NM_144573.4(NEXN):c.2002A>G (p.Ile668Val)	Cardiovascular phenotype [RCV003186936]	uncertain significance	1	77942803	77942803	Human		name
329372792	CV2451659	single nucleotide variant	NM_144573.4(NEXN):c.1693A>G (p.Ile565Val)	Cardiovascular phenotype [RCV004274575]	uncertain significance	1	77942494	77942494	Human		name
329395318	CV2473086	single nucleotide variant	NM_144573.4(NEXN):c.1426G>A (p.Ala476Thr)	not provided [RCV003219070]	uncertain significance	1	77935997	77935997	Human		name
401777343	CV2730288	single nucleotide variant	NM_144573.4(NEXN):c.1898G>C (p.Arg633Thr)	Cardiovascular phenotype [RCV003306347]	uncertain significance	1	77942699	77942699	Human		name
401777344	CV2730289	single nucleotide variant	NM_144573.4(NEXN):c.1202T>C (p.Leu401Pro)	Cardiovascular phenotype [RCV003306348]	uncertain significance	1	77933430	77933430	Human		name
401777351	CV2730292	single nucleotide variant	NM_144573.4(NEXN):c.1924C>G (p.Pro642Ala)	Cardiovascular phenotype [RCV003306351]	uncertain significance	1	77942725	77942725	Human		name
401887011	CV2784427	single nucleotide variant	NM_144573.4(NEXN):c.1855G>A (p.Gly619Arg)	Cardiovascular phenotype [RCV003387403]	uncertain significance	1	77942656	77942656	Human		name
401887013	CV2784428	single nucleotide variant	NM_144573.4(NEXN):c.1666G>C (p.Glu556Gln)	Cardiovascular phenotype [RCV003387404]	uncertain significance	1	77942467	77942467	Human		name
401887014	CV2784429	single nucleotide variant	NM_144573.4(NEXN):c.1004G>A (p.Arg335Lys)	Cardiovascular phenotype [RCV003387405]	uncertain significance	1	77929455	77929455	Human		name
401887016	CV2784430	single nucleotide variant	NM_144573.4(NEXN):c.1948G>A (p.Gly650Arg)	Cardiovascular phenotype [RCV003387406]	uncertain significance	1	77942749	77942749	Human		name
401932013	CV2799014	single nucleotide variant	NM_144573.4(NEXN):c.1898G>A (p.Arg633Lys)	Cardiovascular phenotype [RCV004654208]\|NEXN-related disorder [RCV004531644]	uncertain significance	1	77942699	77942699	Human	1	name , trait , alternate_id
11580125	CV281228	single nucleotide variant	NM_144573.4(NEXN):c.1189C>T (p.Arg397Trp)	Cardiovascular phenotype [RCV002351308]	uncertain significance	1	77933417	77933417	Human		name
11580803	CV281230	single nucleotide variant	NM_144573.4(NEXN):c.1892T>C (p.Ile631Thr)	Cardiovascular phenotype [RCV002411191]\|Dilated Cardiomyopathy, Dominant [RCV000344842]\|Dilated cardiomyopathy 1CC [RCV001850571]\|Hypertrophic cardiomyopathy [RCV000403905]	uncertain significance	1	77942693	77942693	Human	5	name
11650499	CV281842	single nucleotide variant	NM_144573.4(NEXN):c.2021A>C (p.Lys674Thr)	Cardiovascular phenotype [RCV002423277]\|Dilated cardiomyopathy 1CC [RCV002024594]	uncertain significance	1	77942822	77942822	Human	2	name
405239012	CV3081478	single nucleotide variant	NM_144573.4(NEXN):c.1522A>T (p.Thr508Ser)	not provided [RCV003736529]	uncertain significance	1	77942071	77942071	Human		name
405685020	CV3354069	single nucleotide variant	NM_144573.4(NEXN):c.1261G>C (p.Glu421Gln)	Cardiovascular phenotype [RCV004489558]	uncertain significance	1	77935832	77935832	Human		name
405685028	CV3354071	single nucleotide variant	NM_144573.4(NEXN):c.1262A>T (p.Glu421Val)	Cardiovascular phenotype [RCV004489560]	uncertain significance	1	77935833	77935833	Human		name
405685097	CV3354085	single nucleotide variant	NM_144573.4(NEXN):c.1616G>T (p.Arg539Leu)	Cardiovascular phenotype [RCV004489574]	uncertain significance	1	77942165	77942165	Human		name
405685117	CV3354089	single nucleotide variant	NM_144573.4(NEXN):c.1620G>C (p.Met540Ile)	Cardiovascular phenotype [RCV004489578]	uncertain significance	1	77942169	77942169	Human		name
405727873	CV3391081	single nucleotide variant	NM_144573.4(NEXN):c.1078A>G (p.Met360Val)	Cardiovascular phenotype [RCV004524742]	uncertain significance	1	77933306	77933306	Human		name
405727884	CV3391082	single nucleotide variant	NM_144573.4(NEXN):c.1171C>G (p.Arg391Gly)	Cardiovascular phenotype [RCV004524743]\|not provided [RCV005100650]	uncertain significance	1	77933399	77933399	Human		name
405727889	CV3391083	single nucleotide variant	NM_144573.4(NEXN):c.1388T>C (p.Ile463Thr)	Cardiovascular phenotype [RCV004524744]	uncertain significance	1	77935959	77935959	Human		name
405727905	CV3391085	single nucleotide variant	NM_144573.4(NEXN):c.1535A>T (p.Asn512Ile)	Cardiovascular phenotype [RCV004524746]	uncertain significance	1	77942084	77942084	Human		name
405727924	CV3391087	single nucleotide variant	NM_144573.4(NEXN):c.1706C>T (p.Ser569Phe)	Cardiovascular phenotype [RCV004524749]	uncertain significance	1	77942507	77942507	Human		name
405727930	CV3391088	single nucleotide variant	NM_144573.4(NEXN):c.1723G>T (p.Glu575Ter)	Cardiovascular phenotype [RCV004524750]	uncertain significance	1	77942524	77942524	Human		name
405727938	CV3391089	single nucleotide variant	NM_144573.4(NEXN):c.1736C>T (p.Ser579Leu)	Cardiovascular phenotype [RCV004524751]	uncertain significance	1	77942537	77942537	Human		name
405727948	CV3391091	single nucleotide variant	NM_144573.4(NEXN):c.1973A>G (p.Asn658Ser)	Cardiovascular phenotype [RCV004524753]	uncertain significance	1	77942774	77942774	Human		name
405727957	CV3391092	single nucleotide variant	NM_144573.4(NEXN):c.2012T>A (p.Ile671Asn)	Cardiovascular phenotype [RCV004524754]	uncertain significance	1	77942813	77942813	Human		name
407483397	CV3414299	single nucleotide variant	NM_144573.4(NEXN):c.1424G>C (p.Arg475Thr)	Hypertrophic cardiomyopathy 2 [RCV004596635]	not provided	1	77935995	77935995	Human		name
407483401	CV3414300	single nucleotide variant	NM_144573.4(NEXN):c.1426G>C (p.Ala476Pro)	Hypertrophic cardiomyopathy 2 [RCV004596636]	not provided	1	77935997	77935997	Human		name
407526576	CV3451096	single nucleotide variant	NM_144573.4(NEXN):c.1396A>C (p.Lys466Gln)	Cardiovascular phenotype [RCV004654863]	uncertain significance	1	77935967	77935967	Human		name
407489832	CV3451100	single nucleotide variant	NM_144573.4(NEXN):c.1023G>C (p.Lys341Asn)	Cardiovascular phenotype [RCV004641549]	uncertain significance	1	77929474	77929474	Human		name
407526581	CV3451101	single nucleotide variant	NM_144573.4(NEXN):c.1258G>C (p.Glu420Gln)	Cardiovascular phenotype [RCV004654866]	uncertain significance	1	77935829	77935829	Human		name
596926228	CV3536169	single nucleotide variant	NM_144573.4(NEXN):c.1535A>G (p.Asn512Ser)	Dilated cardiomyopathy 1CC [RCV004788599]	uncertain significance	1	77942084	77942084	Human	1	name
596932323	CV3538942	single nucleotide variant	NM_144573.4(NEXN):c.1508G>C (p.Ser503Thr)	not provided [RCV004793068]	uncertain significance	1	77942057	77942057	Human		name
596938566	CV3549518	single nucleotide variant	NM_144573.4(NEXN):c.1172G>A (p.Arg391Gln)	not provided [RCV004812558]	uncertain significance	1	77933400	77933400	Human		name
597698184	CV3565783	single nucleotide variant	NM_144573.4(NEXN):c.1301T>G (p.Leu434Arg)	Cardiovascular phenotype [RCV004987527]	uncertain significance	1	77935872	77935872	Human		name
597698210	CV3565789	single nucleotide variant	NM_144573.4(NEXN):c.1483G>A (p.Val495Ile)	Cardiovascular phenotype [RCV004987533]	likely benign	1	77942032	77942032	Human		name
597698249	CV3565798	single nucleotide variant	NM_144573.4(NEXN):c.1682A>G (p.Glu561Gly)	Cardiovascular phenotype [RCV004987541]	uncertain significance	1	77942483	77942483	Human		name
597698256	CV3565800	single nucleotide variant	NM_144573.4(NEXN):c.1685A>G (p.Glu562Gly)	Cardiovascular phenotype [RCV004987543]	uncertain significance	1	77942486	77942486	Human		name
597698262	CV3565801	single nucleotide variant	NM_144573.4(NEXN):c.1878A>C (p.Glu626Asp)	Cardiovascular phenotype [RCV004987544]	uncertain significance	1	77942679	77942679	Human		name
597698267	CV3565802	single nucleotide variant	NM_144573.4(NEXN):c.1218A>C (p.Gln406His)	Cardiovascular phenotype [RCV004987545]	uncertain significance	1	77933446	77933446	Human		name
598123245	CV3890260	single nucleotide variant	NM_144573.4(NEXN):c.1848G>A (p.Trp616Ter)	not provided [RCV005250779]	uncertain significance	1	77942649	77942649	Human		name
12890193	CV391546	single nucleotide variant	NM_144573.4(NEXN):c.1852G>A (p.Glu618Lys)	Dilated cardiomyopathy 1CC [RCV000474162]\|not provided [RCV004691235]	uncertain significance	1	77942653	77942653	Human	1	name
598254844	CV4000586	single nucleotide variant	NM_144573.4(NEXN):c.1801T>C (p.Phe601Leu)	Cardiovascular phenotype [RCV005385558]	uncertain significance	1	77942602	77942602	Human		name
598232528	CV4000587	single nucleotide variant	NM_144573.4(NEXN):c.1414G>A (p.Ala472Thr)	Cardiovascular phenotype [RCV005381563]	uncertain significance	1	77935985	77935985	Human		name
598232533	CV4000590	single nucleotide variant	NM_144573.4(NEXN):c.1580A>G (p.Glu527Gly)	Cardiovascular phenotype [RCV005381565]	uncertain significance	1	77942129	77942129	Human		name
598232547	CV4000595	single nucleotide variant	NM_144573.4(NEXN):c.1085A>C (p.Lys362Thr)	Cardiovascular phenotype [RCV005381569]	uncertain significance	1	77933313	77933313	Human		name
598254849	CV4000596	single nucleotide variant	NM_144573.4(NEXN):c.1250A>C (p.Glu417Ala)	Cardiovascular phenotype [RCV005385561]	uncertain significance	1	77933478	77933478	Human		name
598232552	CV4000598	single nucleotide variant	NM_144573.4(NEXN):c.1756A>C (p.Lys586Gln)	Cardiovascular phenotype [RCV005381571]	uncertain significance	1	77942557	77942557	Human		name
598232561	CV4000602	single nucleotide variant	NM_144573.4(NEXN):c.1778T>C (p.Val593Ala)	Cardiovascular phenotype [RCV005381574]	uncertain significance	1	77942579	77942579	Human		name
598254854	CV4000604	single nucleotide variant	NM_144573.4(NEXN):c.1297G>A (p.Glu433Lys)	Cardiovascular phenotype [RCV005385563]	uncertain significance	1	77935868	77935868	Human		name
616936444	CV4010515	single nucleotide variant	NM_144573.4(NEXN):c.1432G>C (p.Asp478His)	Cardiovascular phenotype [RCV005403861]	uncertain significance	1	77936003	77936003	Human		name
616937580	CV4011209	single nucleotide variant	NM_144573.4(NEXN):c.1819G>C (p.Gly607Arg)	Cardiovascular phenotype [RCV005405055]	uncertain significance	1	77942620	77942620	Human		name
12892701	CV404750	single nucleotide variant	NM_144573.4(NEXN):c.1687G>T (p.Gly563Cys)	Dilated cardiomyopathy 1CC [RCV000477760]	uncertain significance	1	77942488	77942488	Human	1	name
12899592	CV405244	single nucleotide variant	NM_144573.4(NEXN):c.2005C>T (p.Leu669Phe)	Cardiovascular phenotype [RCV002420246]\|Primary familial hypertrophic cardiomyopathy [RCV000624596]\|not provided [RCV000480554]	uncertain significance	1	77942806	77942806	Human	2	name
12914102	CV421255	single nucleotide variant	NM_144573.4(NEXN):c.1784A>G (p.Asp595Gly)	not provided [RCV000494650]	uncertain significance	1	77942585	77942585	Human		name
13494689	CV448372	single nucleotide variant	NM_144573.4(NEXN):c.1429A>G (p.Ile477Val)	Dilated cardiomyopathy 1CC [RCV000559091]	uncertain significance	1	77936000	77936000	Human	1	name
13476375	CV448375	single nucleotide variant	NM_144573.4(NEXN):c.1997C>A (p.Thr666Asn)	Cardiovascular phenotype [RCV004024151]\|Dilated cardiomyopathy 1CC [RCV000549141]\|not provided [RCV001509042]	uncertain significance	1	77942798	77942798	Human	2	name
13508777	CV485931	single nucleotide variant	NM_144573.4(NEXN):c.1063G>C (p.Asp355His)	Hypertrophic cardiomyopathy 1 [RCV000584821]	uncertain significance	1	77933291	77933291	Human	1	name
13534208	CV509236	single nucleotide variant	NM_144573.4(NEXN):c.1432G>A (p.Asp478Asn)	Cardiovascular phenotype [RCV000618386]\|Dilated cardiomyopathy 1CC [RCV001066584]\|not provided [RCV004767445]	uncertain significance	1	77936003	77936003	Human	2	name
13535037	CV509237	single nucleotide variant	NM_144573.4(NEXN):c.1477G>A (p.Asp493Asn)	Cardiovascular phenotype [RCV000619366]\|Dilated cardiomyopathy 1CC [RCV001855287]\|not provided [RCV005001089]	uncertain significance	1	77942026	77942026	Human	2	name
13529533	CV509238	single nucleotide variant	NM_144573.4(NEXN):c.1481A>T (p.Asp494Val)	Cardiovascular phenotype [RCV000621640]\|Dilated cardiomyopathy 1CC [RCV002498999]	uncertain significance	1	77942030	77942030	Human	2	name
13533500	CV509239	single nucleotide variant	NM_144573.4(NEXN):c.1672G>A (p.Glu558Lys)	Cardiovascular phenotype [RCV000617641]	uncertain significance	1	77942473	77942473	Human		name
13535030	CV509241	single nucleotide variant	NM_144573.4(NEXN):c.1771A>G (p.Thr591Ala)	Cardiovascular phenotype [RCV000619359]\|Dilated cardiomyopathy 1CC [RCV001220795]	likely benign\|uncertain significance	1	77942572	77942572	Human	2	name
13529694	CV509243	single nucleotide variant	NM_144573.4(NEXN):c.2012T>C (p.Ile671Thr)	Cardiovascular phenotype [RCV000621846]\|Dilated cardiomyopathy 1CC [RCV001868102]	uncertain significance	1	77942813	77942813	Human	2	name
13620083	CV516081	single nucleotide variant	NM_144573.4(NEXN):c.1994G>T (p.Ser665Ile)	Dilated cardiomyopathy 1CC [RCV000647287]	uncertain significance	1	77942795	77942795	Human	1	name
13620077	CV516122	single nucleotide variant	NM_144573.4(NEXN):c.1244T>C (p.Met415Thr)	Cardiovascular phenotype [RCV002388113]\|Dilated cardiomyopathy 1CC [RCV000647283]	uncertain significance	1	77933472	77933472	Human	2	name
13796089	CV551691	single nucleotide variant	NM_144573.4(NEXN):c.1108A>G (p.Thr370Ala)	not specified [RCV000678729]	uncertain significance	1	77933336	77933336	Human		name
8610753	CV57051	single nucleotide variant	NM_144573.4(NEXN):c.1112C>T (p.Pro371Leu)	Cardiomyopathy [RCV000183659]\|Cardiovascular phenotype [RCV004018906]\|Dilated cardiomyopathy 1CC [RCV000471176]\|Hypertrophic cardiomyopathy 20 [RCV001253104]\|Primary dilated cardiomyopathy [RCV003993773]\|not provided [RCV000766516]\|not specified [RCV000041157]	uncertain significance	1	77933340	77933340	Human	5	name
8610754	CV57052	single nucleotide variant	NM_144573.4(NEXN):c.1366G>A (p.Gly456Arg)	Dilated cardiomyopathy 1CC [RCV001215702]\|not specified [RCV000041158]	uncertain significance	1	77935937	77935937	Human	1	name
8610757	CV57055	single nucleotide variant	NM_144573.4(NEXN):c.1453G>A (p.Glu485Lys)	Cardiomyopathy [RCV001798220]\|Cardiovascular phenotype [RCV004018907]\|Dilated cardiomyopathy 1CC [RCV001039945]\|Primary dilated cardiomyopathy [RCV001257941]\|not provided [RCV000994029]\|not specified [RCV000041161]	uncertain significance	1	77936024	77936024	Human	5	name
8610758	CV57056	single nucleotide variant	NM_144573.4(NEXN):c.1457C>G (p.Ala486Gly)	Cardiovascular phenotype [RCV003380405]\|Dilated cardiomyopathy 1CC [RCV000816014]\|not provided [RCV001753451]\|not specified [RCV000041162]	uncertain significance	1	77936028	77936028	Human	2	name
8610763	CV57061	single nucleotide variant	NM_144573.4(NEXN):c.1788T>G (p.Ser596Arg)	Cardiomyopathy [RCV000157391]\|Cardiovascular phenotype [RCV003298079]\|Dilated cardiomyopathy 1CC [RCV000232351]\|not provided [RCV000994030]\|not specified [RCV000041167]	likely benign\|conflicting interpretations of pathogenicity\|uncertain significance	1	77942589	77942589	Human	4	name
8610764	CV57062	single nucleotide variant	NM_144573.4(NEXN):c.1937C>A (p.Pro646Gln)	not specified [RCV000041168]	uncertain significance	1	77942738	77942738	Human		name
8610766	CV57064	single nucleotide variant	NM_144573.4(NEXN):c.1996A>G (p.Thr666Ala)	Cardiomyopathy [RCV001170737]\|Cardiovascular phenotype [RCV004018909]\|Dilated cardiomyopathy 1CC [RCV001852835]\|NEXN-related disorder [RCV004734588]\|Primary familial hypertrophic cardiomyopathy [RCV000845374]\|not provided [RCV001699190]\|not specified [RCV0000411 ... (more) 71]	uncertain significance	1	77942797	77942797	Human	6	name , trait , alternate_id
14688771	CV614732	single nucleotide variant	NM_144573.4(NEXN):c.1489G>A (p.Val497Ile)	Cardiomyopathy [RCV000769825]\|Cardiovascular phenotype [RCV003303239]	likely benign\|uncertain significance	1	77942038	77942038	Human	2	name
14688773	CV614733	single nucleotide variant	NM_144573.4(NEXN):c.1550T>A (p.Phe517Tyr)	Cardiomyopathy [RCV000769826]	uncertain significance	1	77942099	77942099	Human	2	name
14688778	CV614735	single nucleotide variant	NM_144573.4(NEXN):c.1585C>A (p.Gln529Lys)	Cardiomyopathy [RCV000769829]	uncertain significance	1	77942134	77942134	Human	2	name
14688365	CV614737	single nucleotide variant	NM_144573.4(NEXN):c.1642G>A (p.Asp548Asn)	Cardiomyopathy [RCV000768804]\|Cardiovascular phenotype [RCV003380706]	uncertain significance	1	77942191	77942191	Human	2	name
14688368	CV614739	single nucleotide variant	NM_144573.4(NEXN):c.1894G>C (p.Glu632Gln)	Cardiomyopathy [RCV000768808]\|Cardiovascular phenotype [RCV002406688]\|Dilated cardiomyopathy 1CC [RCV001218078]	uncertain significance	1	77942695	77942695	Human	4	name
14688369	CV614740	single nucleotide variant	NM_144573.4(NEXN):c.1922T>C (p.Leu641Ser)	Cardiomyopathy [RCV000768809]	uncertain significance	1	77942723	77942723	Human	2	name
14688189	CV620014	single nucleotide variant	NM_144573.4(NEXN):c.1228C>T (p.Gln410Ter)	Cardiovascular phenotype [RCV004649315]\|Dilated cardiomyopathy 1CC [RCV003768437]	pathogenic\|uncertain significance	1	77933456	77933456	Human	2	name
14737301	CV628264	single nucleotide variant	NM_144573.4(NEXN):c.1046G>C (p.Arg349Thr)	Cardiovascular phenotype [RCV002397627]\|Dilated cardiomyopathy 1CC [RCV000804003]	uncertain significance	1	77929497	77929497	Human	2	name
14736567	CV628265	single nucleotide variant	NM_144573.4(NEXN):c.1055T>C (p.Val352Ala)	Cardiovascular phenotype [RCV002397716]\|Dilated cardiomyopathy 1CC [RCV000820077]	uncertain significance	1	77933283	77933283	Human	2	name
14716715	CV628266	single nucleotide variant	NM_144573.4(NEXN):c.1697T>C (p.Met566Thr)	Dilated cardiomyopathy 1CC [RCV000795205]	uncertain significance	1	77942498	77942498	Human	1	name
14741859	CV628267	single nucleotide variant	NM_144573.4(NEXN):c.1739G>A (p.Gly580Glu)	Cardiovascular phenotype [RCV004986639]\|Dilated cardiomyopathy 1CC [RCV000822424]\|Dilated cardiomyopathy 1CC [RCV001328614]\|not provided [RCV002280143]	uncertain significance	1	77942540	77942540	Human	2	name
14744068	CV628268	single nucleotide variant	NM_144573.4(NEXN):c.1877A>G (p.Glu626Gly)	Dilated cardiomyopathy 1CC [RCV000823844]	uncertain significance	1	77942678	77942678	Human	1	name
14725651	CV628269	single nucleotide variant	NM_144573.4(NEXN):c.2008A>T (p.Thr670Ser)	Dilated cardiomyopathy 1CC [RCV000815304]	uncertain significance	1	77942809	77942809	Human	1	name
14975470	CV672381	single nucleotide variant	NM_144573.4(NEXN):c.1123G>T (p.Glu375Ter)	Cardiovascular phenotype [RCV004986652]\|Dilated cardiomyopathy 1CC [RCV002536168]\|Primary familial dilated cardiomyopathy [RCV000845479]	pathogenic\|uncertain significance	1	77933351	77933351	Human	3	name
15015055	CV679528	single nucleotide variant	NM_144573.4(NEXN):c.1619T>C (p.Met540Thr)	Primary dilated cardiomyopathy [RCV000853122]	uncertain significance	1	77942168	77942168	Human	1	name
28912229	CV682594	single nucleotide variant	NM_144573.4(NEXN):c.1175G>A (p.Arg392Gln)	Primary dilated cardiomyopathy [RCV001093571]	likely pathogenic\|uncertain significance	1	77933403	77933403	Human	1	name
28912230	CV682595	single nucleotide variant	NM_144573.4(NEXN):c.1238A>G (p.Gln413Arg)	Primary dilated cardiomyopathy [RCV001093572]	likely pathogenic\|uncertain significance	1	77933466	77933466	Human	1	name
26914361	CV824423	single nucleotide variant	NM_144573.4(NEXN):c.1451G>A (p.Arg484Gln)	Cardiovascular phenotype [RCV004649408]\|Dilated cardiomyopathy 1CC [RCV001040609]\|NEXN-related disorder [RCV004726816]	uncertain significance	1	77936022	77936022	Human	2	name , trait , alternate_id
26908373	CV824424	single nucleotide variant	NM_144573.4(NEXN):c.1928A>C (p.Glu643Ala)	Dilated cardiomyopathy 1CC [RCV001052539]	uncertain significance	1	77942729	77942729	Human	1	name
26886123	CV824425	single nucleotide variant	NM_144573.4(NEXN):c.2014G>A (p.Glu672Lys)	Dilated cardiomyopathy 1CC [RCV001043993]	uncertain significance	1	77942815	77942815	Human	1	name
26902859	CV858247	single nucleotide variant	NM_144573.4(NEXN):c.1529A>G (p.Lys510Arg)	Cardiovascular phenotype [RCV002402489]\|Dilated cardiomyopathy 1CC [RCV001301329]\|Hypertrophic cardiomyopathy 20 [RCV005054331]	uncertain significance	1	77942078	77942078	Human	2	name
38485929	CV922162	single nucleotide variant	NM_144573.4(NEXN):c.1088C>G (p.Thr363Arg)	Cardiovascular phenotype [RCV002418755]\|Dilated cardiomyopathy 1CC [RCV001220070]\|Dilated cardiomyopathy 1CC [RCV003327496]\|not provided [RCV004792812]	uncertain significance	1	77933316	77933316	Human	2	name
38494436	CV952527	single nucleotide variant	NM_144573.4(NEXN):c.1171C>T (p.Arg391Ter)	Cardiovascular phenotype [RCV002327584]\|Dilated cardiomyopathy 1CC [RCV001241310]\|not provided [RCV002224036]	conflicting interpretations of pathogenicity\|uncertain significance	1	77933399	77933399	Human	2	name
39456223	CV966410	single nucleotide variant	NM_144573.4(NEXN):c.1073C>T (p.Pro358Leu)	Cardiovascular phenotype [RCV003166585]\|Dilated cardiomyopathy 1A [RCV001256885]\|Dilated cardiomyopathy 1CC [RCV001366799]\|not provided [RCV001575281]	uncertain significance	1	77933301	77933301	Human	5	name
39456222	CV966411	single nucleotide variant	NM_144573.4(NEXN):c.1695C>G (p.Ile565Met)	Dilated cardiomyopathy 1A [RCV001256884]	uncertain significance	1	77942496	77942496	Human	2	name
126748588	CV987755	single nucleotide variant	NM_144573.4(NEXN):c.1111C>A (p.Pro371Thr)	Dilated cardiomyopathy 1CC [RCV001306463]	uncertain significance	1	77933339	77933339	Human	1	name
126760559	CV987756	single nucleotide variant	NM_144573.4(NEXN):c.1859A>G (p.Glu620Gly)	Cardiovascular phenotype [RCV002411992]\|Dilated cardiomyopathy 1CC [RCV001309351]	uncertain significance	1	77942660	77942660	Human	2	name
126733110	CV1003001	microsatellite	NM_144573.4(NEXN):c.167GAA[1] (p.Arg57del)	Cardiovascular phenotype [RCV003166785]\|Dilated cardiomyopathy 1CC [RCV001313334]	uncertain significance	1	77917703	77917705	Human		name
11647066	CV281862	microsatellite	NM_001172309.1(NEXN):c.709_715TGTTGAG[1]	Dilated Cardiomyopathy, Dominant [RCV000274192]\|Hypertrophic cardiomyopathy [RCV000368786]	likely benign	1	77943536	77943542	Human		name
405727945	CV3391090	microsatellite	NM_144573.4(NEXN):c.184_185dup (p.Arg63fs)	Cardiovascular phenotype [RCV004524752]	uncertain significance	1	77917717	77917718	Human		name
12898639	CV405242	indel	NM_144573.4(NEXN):c.1252-16_1252-12delinsA	not provided [RCV005251140]	likely benign\|uncertain significance	1	77935807	77935811	Human		name
14688357	CV614727	deletion	NM_144573.4(NEXN):c.166_169del (p.Arg56fs)	Cardiomyopathy [RCV000768796]\|Dilated cardiomyopathy 1CC [RCV002536604]	pathogenic\|uncertain significance	1	77917702	77917705	Human	3	name
9690887	CV172460	microsatellite	NM_144573.4(NEXN):c.989AAG[2] (p.Glu332del)	Cardiomyopathy [RCV000769820]\|Cardiovascular phenotype [RCV002381502]\|Dilated cardiomyopathy 1CC [RCV002484953]\|not provided [RCV001699134]\|not specified [RCV000156581]	likely benign\|uncertain significance	1	77929438	77929440	Human		name
155703669	CV1787488	duplication	NM_144573.4(NEXN):c.408_415dup (p.Ile139fs)	Cardiovascular phenotype [RCV002323114]	uncertain significance	1	77918228	77918229	Human		name
10055908	CV198077	deletion	NM_144573.4(NEXN):c.461_464del (p.Asn154fs)	Cardiovascular phenotype [RCV002336468]\|Dilated cardiomyopathy 1CC [RCV001852365]\|not provided [RCV000183676]	pathogenic\|uncertain significance	1	77925199	77925202	Human	2	name
155905724	CV2084173	deletion	NM_144573.4(NEXN):c.354_357del (p.Lys119fs)	Dilated cardiomyopathy 1CC [RCV002858141]	pathogenic	1	77918177	77918180	Human	1	name
405256313	CV3222578	microsatellite	NM_144573.4(NEXN):c.822AGA[2] (p.Glu277del)	Cardiovascular phenotype [RCV004987152]\|Dilated cardiomyopathy 1CC [RCV003986084]\|Dilated cardiomyopathy 1CC [RCV005216161]\|not provided [RCV004784197]	uncertain significance	1	77926850	77926852	Human		name
597842740	CV3865124	microsatellite	NM_144573.4(NEXN):c.518_519del (p.Val173fs)	Dilated cardiomyopathy 1CC [RCV005211572]	pathogenic	1	77926440	77926441	Human		name
8610771	CV57069	deletion	NM_144573.4(NEXN):c.341_342del (p.Gln114fs)	Cardiomyopathy [RCV001170496]\|not provided [RCV001762125]\|not specified [RCV000041176]	uncertain significance	1	77918167	77918168	Human	2	name
126755842	CV1003010	microsatellite	NM_144573.4(NEXN):c.1682AAG[1] (p.Glu562del)	Dilated cardiomyopathy 1CC [RCV001327835]	uncertain significance	1	77942482	77942484	Human		name
150516605	CV1287443	microsatellite	NM_144573.4(NEXN):c.1875AGA[1] (p.Glu626del)	not provided [RCV001723422]	uncertain significance	1	77942676	77942678	Human		name
151830427	CV1362661	microsatellite	NM_144573.4(NEXN):c.1589GAA[1] (p.Arg531del)	Cardiovascular phenotype [RCV005382310]\|Dilated cardiomyopathy 1CC [RCV001993662]\|not provided [RCV003327549]	uncertain significance	1	77942136	77942138	Human		name
155701623	CV1818420	microsatellite	NM_144573.4(NEXN):c.1021AAG[1] (p.Lys342del)	Cardiovascular phenotype [RCV002376556]	uncertain significance	1	77929472	77929474	Human		name
10050023	CV191293	microsatellite	NM_144573.4(NEXN):c.1573GAA[3] (p.Glu528del)	Cardiomyopathy [RCV000769827]\|Cardiovascular phenotype [RCV002390422]\|Dilated cardiomyopathy 1CC [RCV000647277]\|Dilated cardiomyopathy 1CC [RCV003338444]\|NEXN-related disorder [RCV004734778]\|Primary dilated cardiomyopathy [RCV000853115]\|not provided [RCV00065693 ... (more) 0]\|not specified [RCV000183645]	likely benign\|uncertain significance	1	77942121	77942123	Human		name , trait , alternate_id
10055911	CV198090	microsatellite	NM_144573.4(NEXN):c.1416AAG[1] (p.Arg475del)	Cardiomyopathy [RCV001170730]\|Cardiovascular phenotype [RCV000249380]\|Dilated cardiomyopathy 1CC [RCV000458753]\|NEXN-related disorder [RCV004734808]\|Primary familial dilated cardiomyopathy [RCV000845464]\|not provided [RCV001704886]\|not specified [RCV000183679]	likely benign\|conflicting interpretations of pathogenicity\|uncertain significance	1	77935987	77935989	Human		name , trait , alternate_id
10055916	CV198100	microsatellite	NM_144573.4(NEXN):c.1671GGA[3] (p.Glu562del)	Cardiovascular phenotype [RCV002399679]\|Dilated cardiomyopathy 1CC [RCV000463861]\|not provided [RCV000183687]	likely pathogenic\|likely benign\|conflicting interpretations of pathogenicity\|uncertain significance	1	77942470	77942472	Human		name
12901166	CV405243	microsatellite	NM_144573.4(NEXN):c.1478ATG[1] (p.Asp494del)	Cardiovascular phenotype [RCV002395175]\|not provided [RCV000484070]	uncertain significance	1	77942026	77942028	Human		name
8610756	CV57054	microsatellite	NM_144573.4(NEXN):c.1401AGA[2] (p.Glu470del)	Arrhythmogenic right ventricular dysplasia 9 [RCV000491718]\|Cardiovascular phenotype [RCV000621584]\|Dilated cardiomyopathy 1CC [RCV000240639]\|Dilated cardiomyopathy 1CC [RCV000701648]\|not provided [RCV001256889]\|not specified [RCV000041160]	likely pathogenic\|conflicting interpretations of pathogenicity\|uncertain significance	1	77935972	77935974	Human		name
8610760	CV57058	microsatellite	NM_144573.4(NEXN):c.1671GGA[5] (p.Glu562dup)	Cardiovascular phenotype [RCV000621511]\|Dilated cardiomyopathy 1CC [RCV002483027]\|not provided [RCV000767037]\|not specified [RCV000041164]	uncertain significance	1	77942469	77942470	Human		name
8610762	CV57060	microsatellite	NM_144573.4(NEXN):c.1753AAG[1] (p.Lys586del)	Dilated cardiomyopathy 1CC [RCV000795836]\|not provided [RCV001762124]\|not specified [RCV000041166]	uncertain significance	1	77942554	77942556	Human		name
8610765	CV57063	microsatellite	NM_144573.4(NEXN):c.1946GAG[1] (p.Gly650del)	Cardiomyopathy [RCV000768810]\|Cardiovascular phenotype [RCV000251358]\|Dilated cardiomyopathy 1CC [RCV000470679]\|Dilated cardiomyopathy 1CC [RCV000986336]\|NEXN-related disorder [RCV004734587]\|not provided [RCV000766521]\|not specified [RCV000041169]	likely pathogenic\|likely benign\|conflicting interpretations of pathogenicity\|uncertain significance	1	77942746	77942748	Human		name , trait , alternate_id
127289178	CV1151940	deletion	NM_144573.4(NEXN):c.1751_1757del (p.Phe584fs)	not provided [RCV001509041]	uncertain significance	1	77942552	77942558	Human		name
150450578	CV1274970	deletion	NM_144573.4(NEXN):c.1909_1912del (p.Tyr637fs)	Cardiovascular phenotype [RCV003298954]\|not provided [RCV001702175]	likely pathogenic\|uncertain significance	1	77942707	77942710	Human		name
150533628	CV1294285	deletion	NM_144573.4(NEXN):c.1384_1387del (p.Glu462fs)	not provided [RCV001758303]	uncertain significance	1	77935952	77935955	Human		name
9690556	CV172600	microsatellite	NM_144573.4(NEXN):c.1181_1182del (p.Glu394fs)	not specified [RCV000156238]	uncertain significance	1	77933407	77933408	Human		name
155681746	CV1829735	indel	NM_144573.4(NEXN):c.1407delinsGC (p.Glu470fs)	Cardiovascular phenotype [RCV002389400]	uncertain significance	1	77935978	77935978	Human		name
155748096	CV1846552	deletion	NM_144573.4(NEXN):c.2019_2022del (p.Ser673fs)	Cardiovascular phenotype [RCV002417429]	uncertain significance	1	77942817	77942820	Human		name
10055912	CV198093	deletion	NM_144573.4(NEXN):c.1445_1446del (p.Lys482fs)	not provided [RCV000183680]	pathogenic\|uncertain significance	1	77936015	77936016	Human		name
156149339	CV2154340	deletion	NM_144573.4(NEXN):c.1585_1594del (p.Gln529fs)	Dilated cardiomyopathy 1CC [RCV003022797]	uncertain significance	1	77942126	77942135	Human	1	name
11039976	CV224217	deletion	NM_144573.4(NEXN):c.1589_1590del (p.Arg530fs)	Cardiovascular phenotype [RCV003165510]\|Dilated cardiomyopathy 1CC [RCV005222829]\|Left ventricular noncompaction cardiomyopathy [RCV000208121]\|not provided [RCV001770158]	pathogenic\|uncertain significance	1	77942137	77942138	Human	4	name
405007958	CV3109667	insertion	NM_144573.4(NEXN):c.813_814insGG (p.Lys272fs)	Dilated cardiomyopathy 1CC [RCV003804631]	pathogenic	1	77926841	77926842	Human	1	name
13494770	CV448379	deletion	NM_144573.4(NEXN):c.1918_1922del (p.Tyr640fs)	Cardiovascular phenotype [RCV000620168]\|Dilated cardiomyopathy 1CC [RCV000536642]\|not provided [RCV000786389]	likely pathogenic\|uncertain significance	1	77942716	77942720	Human	2	name
13528691	CV509242	microsatellite	NM_144573.4(NEXN):c.1952_1953del (p.Glu651fs)	Cardiovascular phenotype [RCV000620923]	uncertain significance	1	77942750	77942751	Human		name
14693430	CV620015	deletion	NM_144573.4(NEXN):c.1606_1607del (p.Lys536fs)	Dilated cardiomyopathy 1CC [RCV001307654]\|not provided [RCV004723167]	likely pathogenic\|uncertain significance	1	77942153	77942154	Human	1	name
10055910	CV198084	deletion	NM_144573.4(NEXN):c.1002_1004del (p.Arg336del)	Cardiovascular phenotype [RCV002381607]\|not provided [RCV000183678]	uncertain significance	1	77929451	77929453	Human		name
11094363	CV228522	deletion	NM_144573.4(NEXN):c.1820_1822del (p.Gly607del)	Cardiovascular phenotype [RCV002408932]\|Dilated cardiomyopathy 1CC [RCV001069606]\|not provided [RCV000766520]\|not specified [RCV000220963]	uncertain significance	1	77942619	77942621	Human	2	name
11638315	CV267851	insertion	NM_144573.4(NEXN):c.1609_1610insA (p.Leu537fs)	Cardiovascular phenotype [RCV005384689]\|Dilated cardiomyopathy 1CC [RCV002480013]\|Long QT syndrome [RCV001254746]\|not provided [RCV000725298]\|not specified [RCV000301273]	uncertain significance	1	77942158	77942159	Human	4	name
408381769	CV3526594	microsatellite	NM_144573.4(NEXN):c.1480GATGTT[1] (p.494DV[1])	not provided [RCV004771907]	uncertain significance	1	77942028	77942033	Human		name
11542105	CV248626	deletion	NM_144573.3(NEXN):c.1401_1403delAGA (p.Glu470del)	Dilated cardiomyopathy 1CC [RCV000240639]	likely pathogenic	1	77935972	77935974	Human		name
155991292	CV2095487	deletion	NM_144573.4(NEXN):c.586_591del (p.Arg196_Glu197del)	Dilated cardiomyopathy 1CC [RCV002908173]	uncertain significance	1	77926507	77926512	Human	1	name
13620079	CV516090	indel	NM_144573.4(NEXN):c.1901_1904delinsTCT (p.Gly634fs)	Dilated cardiomyopathy 1CC [RCV000647284]	uncertain significance	1	77942702	77942705	Human		name
8610759	CV57057	microsatellite	NM_144573.4(NEXN):c.1671GGA[2] (p.Glu561_Glu562del)	Cardiomyopathy [RCV000768806]\|Cardiovascular phenotype [RCV000618382]\|Dilated cardiomyopathy 1CC [RCV001080274]\|Long QT syndrome [RCV000852586]\|NEXN-related disorder [RCV004541206]\|not provided [RCV000766518]\|not specified [RCV000041163]	likely benign\|conflicting interpretations of pathogenicity\|uncertain significance	1	77942470	77942475	Human		name , trait , alternate_id
329846382	CV2524709	deletion	NM_144573.4(NEXN):c.1668_1673del (p.Glu561_Glu562del)	Dilated cardiomyopathy 1CC [RCV003228189]	uncertain significance	1	77942467	77942472	Human	1	name
156028084	CV2185745	duplication	NM_144573.4(NEXN):c.1535_1537dup (p.Asn512_Met513insAsn)	Dilated cardiomyopathy 1CC [RCV003036060]	uncertain significance	1	77942082	77942083	Human	1	name
401913477	CV2801770	microsatellite	NM_144573.4(NEXN):c.1292_1293del (p.Glu430_Tyr431insTer)	NEXN-related disorder [RCV004529294]	uncertain significance	1	77935861	77935862	Human		name , trait , alternate_id
155721715	CV1828188	insertion	NM_144573.4(NEXN):c.1671_1672insCTT (p.Glu557_Glu558insLeu)	Cardiovascular phenotype [RCV002405852]	uncertain significance	1	77942472	77942473	Human		name
13801413	CV558595	deletion	NM_144573.4(NEXN):c.1664_1666del (p.Arg555_Glu556delinsLys)	Cardiomyopathy [RCV001170734]\|Cardiovascular phenotype [RCV003303159]\|Dilated cardiomyopathy 1CC [RCV000697820]	uncertain significance	1	77942465	77942467	Human	4	name
616937195	CV4011114	indel	NM_144573.4(NEXN):c.475_478delinsTAAA (p.Glu159_Ser160delinsTer)	Cardiovascular phenotype [RCV005404958]	uncertain significance	1	77925215	77925218	Human		name
14688776	CV614734	indel	NM_144573.4(NEXN):c.1582_1585delinsCAAA (p.Glu528_Gln529delinsGlnLys)	Cardiomyopathy [RCV000769828]	uncertain significance	1	77942131	77942134	Human		name
151782186	CV1341979	insertion	NM_144573.4(NEXN):c.1233_1234insGCCGGGCCCGGTGGCTCACGCCTGTAATCCCAGCACATTGGGAGGCCGAGACTGGAGGATCACGAGTTCAGGAGATCGATACCATACANNNNNNNNNNAAAAAAAAAAAAAAAAAAAAAAGAATTTGAACAACTG (p.Arg412delinsAlaGlyProGlyGlySerArgLeuTer)	Dilated cardiomyopathy 1CC [RCV001897348]	pathogenic\|uncertain significance	1	77933444	77933445	Human	1	name

Gene Annotator (Functional Annotation) unavailable	Gene Annotator (Annotation Distribution) unavailable	Variant Visualizer (Genomic Variants) unavailble Variant Visualizer (Genomic Variants) unavailable
Gene Annotator (Functional Annotation)	Gene Annotator (Annotation Distribution)	Variant Visualizer (Genomic Variants)

InterViewer (Protein-Protein Interactions) unavailable	Gviewer (Genome Viewer) unavailable	Variant Visualizer (Damaging Variants) unavailble Variant Visualizer (Damaging Variants) unavailable
InterViewer (Protein-Protein Interactions)	GViewer (Genome Viewer)	Variant Visualizer (Damaging Variants)

Gene Annotator (Annotation Comparison) unavailable	OLGA (Gene List Generator) unavailable
Gene Annotator (Annotation Comparison)	OLGA (Gene List Generator)	Excel (Download)

MOET (Multi-Ontology Enrichement) unavailable	GOLF (Gene-Ortholog Location Finder) unavailable
MOET (Multi-Ontology Enrichement)	GOLF (Gene-Ortholog Location Finder)

Create Name:

Description:

Send us a Message