Nexn Variant Search Result - Rat Genome Database

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795 records found for search term Nexn

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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

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