Dhx37 Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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533 records found for search term Dhx37

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
151356107	CV1328871	single nucleotide variant	NM_032656.4(DHX37):c.-2C>T	not specified [RCV001822460]	uncertain significance	12	124989024	124989024	Human		name
156322107	CV1897933	single nucleotide variant	NM_032656.4(DHX37):c.107-7C>G	not provided [RCV002579314]	likely benign\|uncertain significance	12	124986272	124986272	Human		name
156069724	CV2065721	single nucleotide variant	NM_032656.4(DHX37):c.277-4C>T	not provided [RCV002847037]	likely benign	12	124982627	124982627	Human		name
156036284	CV2097747	single nucleotide variant	NM_032656.4(DHX37):c.888-4C>T	not provided [RCV002885619]	likely benign	12	124975515	124975515	Human		name
155981099	CV2097973	single nucleotide variant	NM_032656.4(DHX37):c.888-5C>T	not provided [RCV002907710]	likely benign	12	124975516	124975516	Human		name
156249558	CV2097974	single nucleotide variant	NM_032656.4(DHX37):c.738+4C>T	DHX37-related disorder [RCV003973510]\|not provided [RCV002895211]	benign	12	124980486	124980486	Human	1	name , trait , alternate_id
156122918	CV2107759	single nucleotide variant	NM_032656.4(DHX37):c.389+9G>A	not provided [RCV002914239]	likely benign	12	124982502	124982502	Human		name
156198096	CV2113790	single nucleotide variant	NM_032656.4(DHX37):c.106+7C>A	not provided [RCV002957281]	benign	12	124988910	124988910	Human		name
155934013	CV2113984	single nucleotide variant	NM_032656.4(DHX37):c.276+4C>T	not provided [RCV002904002]	uncertain significance	12	124986092	124986092	Human		name
156118177	CV2155255	single nucleotide variant	NM_032656.4(DHX37):c.738+8A>G	not provided [RCV003002870]	likely benign	12	124980482	124980482	Human		name
156297898	CV2159321	single nucleotide variant	NM_032656.4(DHX37):c.107-9C>T	not provided [RCV003045413]	likely benign	12	124986274	124986274	Human		name
156323602	CV2173695	single nucleotide variant	NM_032656.4(DHX37):c.981-6A>G	not provided [RCV003046782]	benign	12	124972605	124972605	Human		name
596922620	CV3537313	single nucleotide variant	NM_032656.4(DHX37):c.738+5G>A	not provided [RCV004787283]	uncertain significance	12	124980485	124980485	Human		name
597931726	CV3827143	single nucleotide variant	NM_032656.4(DHX37):c.276+6C>T	not provided [RCV005157156]	uncertain significance	12	124986090	124986090	Human		name
15122640	CV779634	single nucleotide variant	NM_032656.4(DHX37):c.887+9T>C	DHX37-related disorder [RCV003916111]\|not provided [RCV000963104]\|not specified [RCV001819047]	benign	12	124977333	124977333	Human	1	name , trait , alternate_id
150512396	CV1245422	single nucleotide variant	NM_032656.4(DHX37):c.2579-7T>C	46,XY sex reversal 11 [RCV001661412]\|Neurodevelopmental disorder with brain anomalies and with or without vertebral or cardiac anomalies [RCV001661411]\|not provided [RCV002538558]	benign	12	124954003	124954003	Human	3	name
150512399	CV1245425	single nucleotide variant	NM_032656.4(DHX37):c.2046-6A>G	46,XY sex reversal 11 [RCV001661418]\|Neurodevelopmental disorder with brain anomalies and with or without vertebral or cardiac anomalies [RCV001661417]\|not provided [RCV002539630]	benign	12	124960429	124960429	Human	3	name
150512404	CV1245427	single nucleotide variant	NM_032656.4(DHX37):c.738+13G>A	46,XY sex reversal 11 [RCV001661422]\|Neurodevelopmental disorder with brain anomalies and with or without vertebral or cardiac anomalies [RCV001661421]\|not provided [RCV002538559]	benign	12	124980477	124980477	Human	3	name
151352066	CV1322269	single nucleotide variant	NM_032656.4(DHX37):c.1591-1G>C	not provided [RCV001806892]	uncertain significance	12	124965813	124965813	Human		name
151663582	CV1334048	single nucleotide variant	NM_032656.4(DHX37):c.3217-1G>T	Neurodevelopmental disorder with brain anomalies and with or without vertebral or cardiac anomalies [RCV001839222]	likely pathogenic	12	124950060	124950060	Human	1	name
156209034	CV1909626	single nucleotide variant	NM_032656.4(DHX37):c.3216+3A>G	not provided [RCV002595994]	conflicting interpretations of pathogenicity\|uncertain significance	12	124950146	124950146	Human		name
156257541	CV1977399	single nucleotide variant	NM_032656.4(DHX37):c.1735+9C>T	not provided [RCV002597672]	likely benign	12	124965659	124965659	Human		name
156028440	CV2022520	single nucleotide variant	NM_032656.4(DHX37):c.738+16T>C	not provided [RCV002735700]	benign	12	124980474	124980474	Human		name
156030182	CV2022622	single nucleotide variant	NM_032656.4(DHX37):c.276+14G>A	not provided [RCV002735776]	benign	12	124986082	124986082	Human		name
156253872	CV2025856	single nucleotide variant	NM_032656.4(DHX37):c.277-13T>C	not provided [RCV002746083]	benign	12	124982636	124982636	Human		name
156136023	CV2032724	single nucleotide variant	NM_032656.4(DHX37):c.276+13C>T	not provided [RCV002740732]	benign	12	124986083	124986083	Human		name
155965261	CV2034197	single nucleotide variant	NM_032656.4(DHX37):c.1812+7G>A	not provided [RCV002731364]	likely benign	12	124964923	124964923	Human		name
156193551	CV2038088	single nucleotide variant	NM_032656.4(DHX37):c.2983+5C>T	not provided [RCV002765987]	uncertain significance	12	124950685	124950685	Human		name
156270875	CV2055965	single nucleotide variant	NM_032656.4(DHX37):c.2158-5C>A	not provided [RCV002806656]	likely benign	12	124957140	124957140	Human		name
156376644	CV2059717	single nucleotide variant	NM_032656.4(DHX37):c.1812+6C>T	DHX37-related disorder [RCV003973493]\|not provided [RCV002814747]	benign	12	124964924	124964924	Human	1	name , trait , alternate_id
156160447	CV2060226	single nucleotide variant	NM_032656.4(DHX37):c.2695+4C>A	not provided [RCV002801611]	uncertain significance	12	124953876	124953876	Human		name
155989835	CV2105687	single nucleotide variant	NM_032656.4(DHX37):c.1191+9G>A	not provided [RCV002947279]	likely benign	12	124971293	124971293	Human		name
156015861	CV2114406	single nucleotide variant	NM_032656.4(DHX37):c.2157+4A>G	not provided [RCV002909361]	uncertain significance	12	124960308	124960308	Human		name
156386248	CV2125544	single nucleotide variant	NM_032656.4(DHX37):c.887+10G>A	not provided [RCV002943507]	likely benign	12	124977332	124977332	Human		name
155951498	CV2133234	single nucleotide variant	NM_032656.4(DHX37):c.738+12C>T	not provided [RCV002994656]	likely benign	12	124980478	124980478	Human		name
156012953	CV2137462	single nucleotide variant	NM_032656.4(DHX37):c.887+13C>T	not provided [RCV003017841]	likely benign	12	124977329	124977329	Human		name
156020699	CV2141252	single nucleotide variant	NM_032656.4(DHX37):c.2579-9G>A	not provided [RCV002976139]	benign	12	124954005	124954005	Human		name
155958325	CV2159352	single nucleotide variant	NM_032656.4(DHX37):c.107-14C>G	not provided [RCV003015226]	likely benign	12	124986279	124986279	Human		name
156165425	CV2169582	single nucleotide variant	NM_032656.4(DHX37):c.1591-5C>T	not provided [RCV003023347]	likely benign	12	124965817	124965817	Human		name
156323586	CV2173693	single nucleotide variant	NM_032656.4(DHX37):c.1409-3C>T	DHX37-related disorder [RCV003973627]\|not provided [RCV003046781]	benign	12	124967221	124967221	Human	1	name , trait , alternate_id
156402906	CV2189621	deletion	NM_032656.4(DHX37):c.2984-3del	not provided [RCV003052491]	benign	12	124950553	124950553	Human		name
405161587	CV2950284	single nucleotide variant	NM_032656.4(DHX37):c.1192-9C>T	not provided [RCV003674654]	likely benign	12	124968977	124968977	Human		name
402503782	CV3006950	single nucleotide variant	NM_032656.4(DHX37):c.3290+8C>T	not provided [RCV003688641]	likely benign	12	124949978	124949978	Human		name
405147614	CV3024050	single nucleotide variant	NM_032656.4(DHX37):c.277-14G>C	not provided [RCV003702997]	likely benign	12	124982637	124982637	Human		name
402479169	CV3033025	single nucleotide variant	NM_032656.4(DHX37):c.276+15G>A	not provided [RCV003712588]	likely benign	12	124986081	124986081	Human		name
405185451	CV3057894	single nucleotide variant	NM_032656.4(DHX37):c.2265-8A>G	not provided [RCV003729090]	likely benign	12	124956887	124956887	Human		name
596926944	CV3530914	single nucleotide variant	NM_032656.4(DHX37):c.1408+1G>A	not provided [RCV004778499]	uncertain significance	12	124968533	124968533	Human		name
597891142	CV3749345	single nucleotide variant	NM_032656.4(DHX37):c.2453+5G>A	not provided [RCV005071129]	uncertain significance	12	124956686	124956686	Human		name
597969305	CV3761284	single nucleotide variant	NM_032656.4(DHX37):c.1505-8T>A	not provided [RCV005083671]	likely benign	12	124966886	124966886	Human		name
597856803	CV3769403	single nucleotide variant	NM_032656.4(DHX37):c.1591-7G>A	not provided [RCV005105444]	likely benign	12	124965819	124965819	Human		name
597976361	CV3829579	single nucleotide variant	NM_032656.4(DHX37):c.3122-7C>T	not provided [RCV005169846]	likely benign	12	124950250	124950250	Human		name
597832242	CV3830945	single nucleotide variant	NM_032656.4(DHX37):c.2264+6G>T	not provided [RCV005170342]	uncertain significance	12	124957023	124957023	Human		name
597894454	CV3833549	single nucleotide variant	NM_032656.4(DHX37):c.981-17G>A	not provided [RCV005180241]	likely benign	12	124972616	124972616	Human		name
597964303	CV3848014	single nucleotide variant	NM_032656.4(DHX37):c.1591-4G>A	not provided [RCV005193893]	likely benign	12	124965816	124965816	Human		name
598123765	CV3890439	single nucleotide variant	NM_032656.4(DHX37):c.2696-2A>G	not provided [RCV005250958]	uncertain significance	12	124952572	124952572	Human		name
150512385	CV1245417	single nucleotide variant	NM_032656.4(DHX37):c.2869-38G>A	46,XY sex reversal 11 [RCV001661402]\|Neurodevelopmental disorder with brain anomalies and with or without vertebral or cardiac anomalies [RCV001661401]\|not provided [RCV004707671]	benign	12	124950842	124950842	Human	3	name
150512387	CV1245418	single nucleotide variant	NM_032656.4(DHX37):c.2696-26G>A	46,XY sex reversal 11 [RCV001661404]\|Neurodevelopmental disorder with brain anomalies and with or without vertebral or cardiac anomalies [RCV001661403]\|not provided [RCV004709119]	benign	12	124952596	124952596	Human	3	name
150512388	CV1245419	single nucleotide variant	NM_032656.4(DHX37):c.2695+12T>C	46,XY sex reversal 11 [RCV001661406]\|Neurodevelopmental disorder with brain anomalies and with or without vertebral or cardiac anomalies [RCV001661405]\|not provided [RCV002539629]	benign	12	124953868	124953868	Human	3	name
150512398	CV1245423	single nucleotide variant	NM_032656.4(DHX37):c.2578+17T>G	46,XY sex reversal 11 [RCV001661414]\|Neurodevelopmental disorder with brain anomalies and with or without vertebral or cardiac anomalies [RCV001661413]\|not provided [RCV001762735]	benign	12	124954070	124954070	Human	3	name
150512402	CV1245426	single nucleotide variant	NM_032656.4(DHX37):c.1294-38T>C	46,XY sex reversal 11 [RCV001661420]\|Neurodevelopmental disorder with brain anomalies and with or without vertebral or cardiac anomalies [RCV001661419]\|not provided [RCV004709120]	benign	12	124968686	124968686	Human	3	name
156078862	CV1975637	single nucleotide variant	NM_032656.4(DHX37):c.3388+12C>T	not provided [RCV002621477]	benign	12	124948072	124948072	Human		name
156078567	CV2022513	single nucleotide variant	NM_032656.4(DHX37):c.1077+11G>C	not provided [RCV002760549]	benign	12	124972492	124972492	Human		name
156030157	CV2022621	single nucleotide variant	NM_032656.4(DHX37):c.3389-11C>T	not provided [RCV002735775]	benign	12	124947898	124947898	Human		name
156079779	CV2022661	single nucleotide variant	NM_032656.4(DHX37):c.2453+14G>A	not provided [RCV002760587]	benign	12	124956677	124956677	Human		name
156133140	CV2022826	single nucleotide variant	NM_032656.4(DHX37):c.1813-19T>C	not provided [RCV002740638]	likely benign	12	124964645	124964645	Human		name
156133469	CV2022838	single nucleotide variant	NM_032656.4(DHX37):c.1812+17G>A	not provided [RCV002740648]	benign	12	124964913	124964913	Human		name
156275926	CV2023508	single nucleotide variant	NM_032656.4(DHX37):c.2264+19G>A	not provided [RCV002746799]	likely benign	12	124957010	124957010	Human		name
155961975	CV2023740	single nucleotide variant	NM_032656.4(DHX37):c.2578+16G>A	not provided [RCV002731219]	likely benign	12	124954071	124954071	Human		name
156041830	CV2026417	single nucleotide variant	NM_032656.4(DHX37):c.1409-15C>T	not provided [RCV002736214]	likely benign	12	124967233	124967233	Human		name
156247101	CV2029439	single nucleotide variant	NM_032656.4(DHX37):c.3290+15G>A	not provided [RCV002745863]	likely benign	12	124949971	124949971	Human		name
155912555	CV2029574	single nucleotide variant	NM_032656.4(DHX37):c.2264+13G>A	not provided [RCV002750247]	benign	12	124957016	124957016	Human		name
156250478	CV2029583	single nucleotide variant	NM_032656.4(DHX37):c.2869-13C>T	not provided [RCV002745969]	likely benign	12	124950817	124950817	Human		name
156046824	CV2030915	single nucleotide variant	NM_032656.4(DHX37):c.2695+15C>T	not provided [RCV002736377]	likely benign	12	124953865	124953865	Human		name
156136552	CV2032745	single nucleotide variant	NM_032656.4(DHX37):c.3216+11C>G	not provided [RCV002740750]	benign	12	124950138	124950138	Human		name
155910123	CV2032800	single nucleotide variant	NM_032656.4(DHX37):c.2265-11T>A	not provided [RCV002750072]	likely benign	12	124956890	124956890	Human		name
156143108	CV2033024	single nucleotide variant	NM_032656.4(DHX37):c.2158-17G>A	not provided [RCV002740967]	likely benign	12	124957152	124957152	Human		name
155955847	CV2033402	single nucleotide variant	NM_032656.4(DHX37):c.2453+13C>T	not provided [RCV002730923]	likely benign	12	124956678	124956678	Human		name
156160552	CV2033826	single nucleotide variant	NM_032656.4(DHX37):c.3290+11C>T	not provided [RCV002741529]	likely benign	12	124949975	124949975	Human		name
155929357	CV2041717	single nucleotide variant	NM_032656.4(DHX37):c.3216+14C>T	not provided [RCV002751079]	likely benign	12	124950135	124950135	Human		name
156107019	CV2072269	single nucleotide variant	NM_032656.4(DHX37):c.3291-20C>T	not provided [RCV002870748]	likely benign	12	124948201	124948201	Human		name
155931905	CV2096119	single nucleotide variant	NM_032656.4(DHX37):c.2157+10T>C	not provided [RCV002903876]	benign	12	124960302	124960302	Human		name
156096283	CV2110593	single nucleotide variant	NM_032656.4(DHX37):c.2158-19A>G	not provided [RCV002926872]	likely benign	12	124957154	124957154	Human		name
156296830	CV2111702	single nucleotide variant	NM_032656.4(DHX37):c.2984-10C>T	not provided [RCV002922385]	likely benign	12	124950560	124950560	Human		name
156392675	CV2123583	single nucleotide variant	NM_032656.4(DHX37):c.2046-18C>T	not provided [RCV002944071]	likely benign	12	124960441	124960441	Human		name
156028087	CV2125269	single nucleotide variant	NM_032656.4(DHX37):c.3122-11C>T	not provided [RCV002949103]	likely benign	12	124950254	124950254	Human		name
156372610	CV2127655	single nucleotide variant	NM_032656.4(DHX37):c.3121+15T>C	not provided [RCV002942456]	likely benign	12	124950398	124950398	Human		name
156301556	CV2146207	single nucleotide variant	NM_032656.4(DHX37):c.1591-17T>C	not provided [RCV003010409]	likely benign\|uncertain significance	12	124965829	124965829	Human		name
156041067	CV2146800	single nucleotide variant	NM_032656.4(DHX37):c.1293+20C>T	not provided [RCV003019059]	likely benign	12	124968847	124968847	Human		name
155933477	CV2153265	single nucleotide variant	NM_032656.4(DHX37):c.2695+20C>A	not provided [RCV003013771]	likely benign	12	124953860	124953860	Human		name
156209355	CV2175572	single nucleotide variant	NM_032656.4(DHX37):c.3290+12G>T	not provided [RCV003024746]	likely benign	12	124949974	124949974	Human		name
405236626	CV2973328	single nucleotide variant	NM_032656.4(DHX37):c.1293+10G>A	not provided [RCV003683103]	likely benign	12	124968857	124968857	Human		name
405047123	CV3014315	single nucleotide variant	NM_032656.4(DHX37):c.2453+20G>C	not provided [RCV003696740]	likely benign	12	124956671	124956671	Human		name
405062946	CV3020511	single nucleotide variant	NM_032656.4(DHX37):c.3290+12G>A	not provided [RCV003697763]	likely benign	12	124949974	124949974	Human		name
405064146	CV3020621	single nucleotide variant	NM_032656.4(DHX37):c.1504+12G>A	not provided [RCV003697836]	likely benign	12	124967111	124967111	Human		name
405064968	CV3020713	single nucleotide variant	NM_032656.4(DHX37):c.2983+14C>T	not provided [RCV003697896]	likely benign	12	124950676	124950676	Human		name
405065200	CV3020731	single nucleotide variant	NM_032656.4(DHX37):c.1191+17G>A	not provided [RCV003697908]	likely benign	12	124971285	124971285	Human		name
405144817	CV3027221	single nucleotide variant	NM_032656.4(DHX37):c.3121+13A>G	not provided [RCV003702732]	likely benign	12	124950400	124950400	Human		name
405180278	CV3027671	single nucleotide variant	NM_032656.4(DHX37):c.3216+15G>A	not provided [RCV003705379]	likely benign	12	124950134	124950134	Human		name
405153414	CV3027901	single nucleotide variant	NM_032656.4(DHX37):c.1590+12G>A	not provided [RCV003703447]	likely benign	12	124966781	124966781	Human		name
405119873	CV3030651	single nucleotide variant	NM_032656.4(DHX37):c.2265-18C>A	not provided [RCV003700584]	benign	12	124956897	124956897	Human		name
405203530	CV3036375	single nucleotide variant	NM_032656.4(DHX37):c.2695+20C>T	not provided [RCV003707641]	likely benign	12	124953860	124953860	Human		name
405197745	CV3037872	single nucleotide variant	NM_032656.4(DHX37):c.1409-17G>A	not provided [RCV003707061]	likely benign	12	124967235	124967235	Human		name
402500046	CV3038341	single nucleotide variant	NM_032656.4(DHX37):c.1504+17G>A	not provided [RCV003714574]	likely benign	12	124967106	124967106	Human		name
405200542	CV3041153	single nucleotide variant	NM_032656.4(DHX37):c.3217-18C>T	not provided [RCV003707338]	likely benign	12	124950077	124950077	Human		name
597895179	CV3806298	single nucleotide variant	NM_032656.4(DHX37):c.1812+16C>T	not provided [RCV005151881]	likely benign	12	124964914	124964914	Human		name
597933073	CV3810653	single nucleotide variant	NM_032656.4(DHX37):c.1191+12G>A	not provided [RCV005157362]	likely benign	12	124971290	124971290	Human		name
156042579	CV2094195	deletion	NM_032656.4(DHX37):c.106+7_106+8del	not provided [RCV002885870]	benign	12	124988909	124988910	Human		name
156111986	CV2177438	duplication	NM_032656.4(DHX37):c.2263_2264+1dup	not provided [RCV003055129]	uncertain significance	12	124957027	124957028	Human		name
156210064	CV1987151	inversion	NM_032656.4(DHX37):c.2046-7_2046-6inv	not provided [RCV002626045]	uncertain significance	12	124960429	124960430	Human		name
156170506	CV2056791	microsatellite	NM_032656.4(DHX37):c.107-11_107-10del	not provided [RCV002801938]	uncertain significance	12	124986275	124986276	Human		name
405193478	CV2975092	deletion	NM_032656.4(DHX37):c.2454-6_2454-5del	not provided [RCV003677422]	uncertain significance	12	124954216	124954217	Human		name
405233396	CV2981759	deletion	NM_032656.4(DHX37):c.888-35_888-19del	not provided [RCV003711887]	likely benign	12	124975530	124975546	Human		name
15195475	CV724980	single nucleotide variant	NM_032656.4(DHX37):c.42G>A (p.Gln14=)	DHX37-related disorder [RCV003957924]\|not provided [RCV000889514]	benign\|likely benign	12	124988981	124988981	Human	1	name , trait , alternate_id
156340107	CV2106914	single nucleotide variant	NM_032656.4(DHX37):c.141C>T (p.Asn47=)	not provided [RCV002938850]	likely benign	12	124986231	124986231	Human		name
156253405	CV2117099	single nucleotide variant	NM_032656.4(DHX37):c.153A>C (p.Leu51=)	not provided [RCV002933631]	likely benign	12	124986219	124986219	Human		name
329394630	CV2472898	duplication	NM_032656.4(DHX37):c.75dup (p.Glu26fs)	not provided [RCV003218881]	uncertain significance	12	124988947	124988948	Human		name
402502765	CV3006999	single nucleotide variant	NM_032656.4(DHX37):c.14G>T (p.Arg5Leu)	not provided [RCV003688671]	uncertain significance	12	124989009	124989009	Human		name
405198609	CV3032701	single nucleotide variant	NM_032656.4(DHX37):c.214C>T (p.Leu72=)	not provided [RCV003707133]	likely benign	12	124986158	124986158	Human		name
598123421	CV3890333	deletion	NM_032656.4(DHX37):c.75del (p.Glu26fs)	not provided [RCV005250852]	uncertain significance	12	124988948	124988948	Human		name
156387437	CV1888146	single nucleotide variant	NM_032656.4(DHX37):c.816C>T (p.Ile272=)	DHX37-related disorder [RCV003943746]\|not provided [RCV003067679]	likely benign	12	124977413	124977413	Human	1	name , trait , alternate_id
156160932	CV1906900	single nucleotide variant	NM_032656.4(DHX37):c.633G>A (p.Pro211=)	not provided [RCV003082891]	likely benign	12	124980595	124980595	Human		name
156386289	CV1961278	single nucleotide variant	NM_032656.4(DHX37):c.690G>A (p.Leu230=)	not provided [RCV002583510]	likely benign	12	124980538	124980538	Human		name
156275694	CV2023490	single nucleotide variant	NM_032656.4(DHX37):c.582C>G (p.Thr194=)	not provided [RCV002746792]	likely benign	12	124980646	124980646	Human		name
156084727	CV2023772	single nucleotide variant	NM_032656.4(DHX37):c.933C>T (p.Ala311=)	not provided [RCV002760741]	likely benign	12	124975466	124975466	Human		name
155988723	CV2026798	single nucleotide variant	NM_032656.4(DHX37):c.441C>T (p.Ser147=)	not provided [RCV002755654]	likely benign	12	124980787	124980787	Human		name
156244931	CV2029344	inversion	NM_032656.4(DHX37):c.2695+12_2695+13inv	not provided [RCV002745794]	uncertain significance	12	124953867	124953868	Human		name
156083780	CV2060343	single nucleotide variant	NM_032656.4(DHX37):c.62C>G (p.Ser21Trp)	not provided [RCV002823942]	uncertain significance	12	124988961	124988961	Human		name
156226833	CV2088803	single nucleotide variant	NM_032656.4(DHX37):c.70C>A (p.Pro24Thr)	not provided [RCV002876084]	uncertain significance	12	124988953	124988953	Human		name
155981120	CV2097975	single nucleotide variant	NM_032656.4(DHX37):c.573T>C (p.Gly191=)	not provided [RCV002907711]	benign	12	124980655	124980655	Human		name
156300227	CV2104899	single nucleotide variant	NM_032656.4(DHX37):c.912G>A (p.Thr304=)	not provided [RCV002922539]	likely benign	12	124975487	124975487	Human		name
156004052	CV2130323	single nucleotide variant	NM_032656.4(DHX37):c.339T>C (p.Phe113=)	not provided [RCV002975319]	likely benign	12	124982561	124982561	Human		name
155960570	CV2131793	single nucleotide variant	NM_032656.4(DHX37):c.633G>T (p.Pro211=)	not provided [RCV002995134]	likely benign	12	124980595	124980595	Human		name
156012512	CV2137375	single nucleotide variant	NM_032656.4(DHX37):c.801G>A (p.Glu267=)	not provided [RCV003017820]	likely benign	12	124977428	124977428	Human		name
155945861	CV2139434	single nucleotide variant	NM_032656.4(DHX37):c.627C>A (p.Pro209=)	not provided [RCV002994337]	likely benign	12	124980601	124980601	Human		name
156315156	CV2158565	single nucleotide variant	NM_032656.4(DHX37):c.37C>A (p.Arg13Ser)	not provided [RCV003028815]	uncertain significance	12	124988986	124988986	Human		name
156178585	CV2298308	single nucleotide variant	NM_032656.4(DHX37):c.71C>G (p.Pro24Arg)	Inborn genetic diseases [RCV002891833]	uncertain significance	12	124988952	124988952	Human	1	name
401881070	CV2789482	single nucleotide variant	NM_032656.4(DHX37):c.53C>T (p.Pro18Leu)	Inborn genetic diseases [RCV003385224]	uncertain significance	12	124988970	124988970	Human	1	name
401934101	CV2817121	single nucleotide variant	NM_032656.4(DHX37):c.729G>A (p.Pro243=)	not provided [RCV003410960]	likely benign	12	124980499	124980499	Human		name
401943464	CV2840053	single nucleotide variant	NM_032656.4(DHX37):c.405G>A (p.Val135=)	not provided [RCV003456840]	likely benign	12	124980823	124980823	Human		name
405120317	CV2952221	single nucleotide variant	NM_032656.4(DHX37):c.627C>T (p.Pro209=)	not provided [RCV003671359]	likely benign	12	124980601	124980601	Human		name
405054654	CV3022330	single nucleotide variant	NM_032656.4(DHX37):c.750G>A (p.Leu250=)	not provided [RCV003697175]	likely benign	12	124977479	124977479	Human		name
405143546	CV3027215	duplication	NM_032656.4(DHX37):c.1736-17_1736-15dup	not provided [RCV003702727]	likely benign	12	124965020	124965021	Human		name
402510359	CV3042440	single nucleotide variant	NM_032656.4(DHX37):c.318C>T (p.Ser106=)	not provided [RCV003715581]	likely benign	12	124982582	124982582	Human		name
405254737	CV3051802	single nucleotide variant	NM_032656.4(DHX37):c.837C>T (p.Ser279=)	not provided [RCV003723065]	likely benign	12	124977392	124977392	Human		name
405108142	CV3136560	single nucleotide variant	NM_032656.4(DHX37):c.699C>G (p.Pro233=)	not provided [RCV003835714]	likely benign	12	124980529	124980529	Human		name
597658070	CV3652402	single nucleotide variant	NM_032656.4(DHX37):c.88G>T (p.Val30Leu)	Inborn genetic diseases [RCV004976840]\|not provided [RCV005110176]	uncertain significance	12	124988935	124988935	Human	1	name
597878785	CV3763249	single nucleotide variant	NM_032656.4(DHX37):c.912G>C (p.Thr304=)	not provided [RCV005108844]	likely benign	12	124975487	124975487	Human		name
597893393	CV3763490	single nucleotide variant	NM_032656.4(DHX37):c.768C>T (p.Ser256=)	not provided [RCV005111070]	likely benign	12	124977461	124977461	Human		name
597958741	CV3814912	single nucleotide variant	NM_032656.4(DHX37):c.47C>A (p.Ala16Glu)	not provided [RCV005163037]	uncertain significance	12	124988976	124988976	Human		name
597915328	CV3817657	single nucleotide variant	NM_032656.4(DHX37):c.654T>C (p.Pro218=)	not provided [RCV005154859]	likely benign	12	124980574	124980574	Human		name
597895924	CV3834528	single nucleotide variant	NM_032656.4(DHX37):c.972G>T (p.Leu324=)	not provided [RCV005180439]	likely benign	12	124975427	124975427	Human		name
15187489	CV738539	single nucleotide variant	NM_032656.4(DHX37):c.831C>T (p.Thr277=)	DHX37-related disorder [RCV003932950]\|not provided [RCV000909103]	benign	12	124977398	124977398	Human	1	name , trait , alternate_id
15187492	CV738540	single nucleotide variant	NM_032656.4(DHX37):c.714C>T (p.Pro238=)	DHX37-related disorder [RCV003932951]\|not provided [RCV000909104]	benign	12	124980514	124980514	Human	1	name , trait , alternate_id
150331920	CV1163578	single nucleotide variant	NM_032656.4(DHX37):c.2025G>A (p.Thr675=)	not provided [RCV001528004]	benign	12	124964414	124964414	Human		name
150503937	CV1240654	single nucleotide variant	NM_032656.4(DHX37):c.2793A>G (p.Ala931=)	46,XY sex reversal 11 [RCV001658393]\|Neurodevelopmental disorder with brain anomalies and with or without vertebral or cardiac anomalies [RCV001658392]\|not provided [RCV001657497]	benign	12	124952473	124952473	Human	3	name
150512393	CV1245421	single nucleotide variant	NM_032656.4(DHX37):c.2598G>A (p.Glu866=)	46,XY sex reversal 11 [RCV001661410]\|Neurodevelopmental disorder with brain anomalies and with or without vertebral or cardiac anomalies [RCV001661409]\|not provided [RCV002538557]	benign	12	124953977	124953977	Human	3	name
150436635	CV1245424	single nucleotide variant	NM_032656.4(DHX37):c.2331A>G (p.Thr777=)	46,XY sex reversal 11 [RCV001661416]\|DHX37-related disorder [RCV003984038]\|Neurodevelopmental disorder with brain anomalies and with or without vertebral or cardiac anomalies [RCV001661415]\|not provided [RCV001694159]	benign	12	124956813	124956813	Human	3	name , trait , alternate_id
150512407	CV1245428	single nucleotide variant	NM_032656.4(DHX37):c.288G>A (p.Met96Ile)	46,XY sex reversal 11 [RCV001661424]\|DHX37-related disorder [RCV003984039]\|Neurodevelopmental disorder with brain anomalies and with or without vertebral or cardiac anomalies [RCV001661423]\|not provided [RCV002539631]	benign	12	124982612	124982612	Human	3	name , trait , alternate_id
150447714	CV1270351	single nucleotide variant	NM_032656.4(DHX37):c.2343A>G (p.Ala781=)	DHX37-related disorder [RCV003921341]\|not provided [RCV001691488]	benign	12	124956801	124956801	Human	1	name , trait , alternate_id
150545313	CV1293129	single nucleotide variant	NM_032656.4(DHX37):c.2499G>T (p.Arg833=)	DHX37-related disorder [RCV003968528]\|not provided [RCV001762915]	benign	12	124954166	124954166	Human	1	name , trait , alternate_id
156285626	CV1884798	single nucleotide variant	NM_032656.4(DHX37):c.1374G>A (p.Arg458=)	not provided [RCV003061232]	likely benign	12	124968568	124968568	Human		name
156040652	CV1891013	single nucleotide variant	NM_032656.4(DHX37):c.1938C>T (p.Tyr646=)	not provided [RCV003078503]	likely benign	12	124964501	124964501	Human		name
156334775	CV1905909	single nucleotide variant	NM_032656.4(DHX37):c.1125C>T (p.His375=)	not provided [RCV003090005]	likely benign	12	124971368	124971368	Human		name
156018833	CV1909321	single nucleotide variant	NM_032656.4(DHX37):c.1362C>T (p.Gly454=)	not provided [RCV002619286]	benign	12	124968580	124968580	Human		name
156044935	CV1914776	single nucleotide variant	NM_032656.4(DHX37):c.1530G>A (p.Ser510=)	not provided [RCV002620401]	likely benign	12	124966853	124966853	Human		name
156406129	CV1921467	single nucleotide variant	NM_032656.4(DHX37):c.1215C>T (p.Leu405=)	not provided [RCV002606497]	likely benign	12	124968945	124968945	Human		name
156061428	CV1925641	single nucleotide variant	NM_032656.4(DHX37):c.227A>G (p.Glu76Gly)	not provided [RCV002620960]	uncertain significance	12	124986145	124986145	Human		name
156168542	CV1930085	single nucleotide variant	NM_032656.4(DHX37):c.106G>A (p.Asp36Asn)	not provided [RCV002624629]	uncertain significance	12	124988917	124988917	Human		name
155951450	CV1936093	single nucleotide variant	NM_032656.4(DHX37):c.1638C>T (p.Gly546=)	DHX37-related disorder [RCV003943415]\|not provided [RCV002511746]	likely benign	12	124965765	124965765	Human	1	name , trait , alternate_id
156441995	CV1941728	single nucleotide variant	NM_032656.4(DHX37):c.2538G>A (p.Gln846=)	not provided [RCV003112331]	likely benign	12	124954127	124954127	Human		name
156082059	CV2023614	insertion	NM_032656.4(DHX37):c.1504+12_1504+13insT	not provided [RCV002760658]	likely benign	12	124967110	124967111	Human		name
155951358	CV2026242	single nucleotide variant	NM_032656.4(DHX37):c.2559C>A (p.Gly853=)	not provided [RCV002730697]	likely benign	12	124954106	124954106	Human		name
156044784	CV2026545	single nucleotide variant	NM_032656.4(DHX37):c.2880C>T (p.Leu960=)	not provided [RCV002736313]	uncertain significance	12	124950793	124950793	Human		name
156048840	CV2027175	single nucleotide variant	NM_032656.4(DHX37):c.1776G>A (p.Pro592=)	not provided [RCV002736443]	likely benign	12	124964966	124964966	Human		name
156141056	CV2032935	single nucleotide variant	NM_032656.4(DHX37):c.2352C>T (p.Tyr784=)	not provided [RCV002740900]	likely benign	12	124956792	124956792	Human		name
156186817	CV2033908	single nucleotide variant	NM_032656.4(DHX37):c.1230G>A (p.Thr410=)	not provided [RCV002765788]	likely benign	12	124968930	124968930	Human		name
156187514	CV2033943	single nucleotide variant	NM_032656.4(DHX37):c.1452G>A (p.Ala484=)	not provided [RCV002765806]	likely benign	12	124967175	124967175	Human		name
156147327	CV2037430	single nucleotide variant	NM_032656.4(DHX37):c.2109G>A (p.Arg703=)	not provided [RCV002786734]	likely benign	12	124960360	124960360	Human		name
156065113	CV2065542	single nucleotide variant	NM_032656.4(DHX37):c.2055A>C (p.Ser685=)	not provided [RCV002846900]	likely benign	12	124960414	124960414	Human		name
156353396	CV2066044	single nucleotide variant	NM_032656.4(DHX37):c.194C>T (p.Ser65Leu)	not provided [RCV002811950]	uncertain significance	12	124986178	124986178	Human		name
156326431	CV2098324	single nucleotide variant	NM_032656.4(DHX37):c.1284G>A (p.Pro428=)	DHX37-related disorder [RCV003903804]\|not provided [RCV002899657]	benign	12	124968876	124968876	Human	1	name , trait , alternate_id
155924062	CV2099463	single nucleotide variant	NM_032656.4(DHX37):c.2994C>T (p.Ser998=)	not provided [RCV002903484]	benign	12	124950540	124950540	Human		name
156128220	CV2100707	single nucleotide variant	NM_032656.4(DHX37):c.2181G>A (p.Thr727=)	not provided [RCV002889840]	likely benign	12	124957112	124957112	Human		name
155979104	CV2101483	single nucleotide variant	NM_032656.4(DHX37):c.2265G>A (p.Arg755=)	not provided [RCV002907615]	uncertain significance	12	124956879	124956879	Human		name
156241879	CV2101489	single nucleotide variant	NM_032656.4(DHX37):c.1269C>T (p.Phe423=)	DHX37-related disorder [RCV003926457]\|not provided [RCV002894941]	benign	12	124968891	124968891	Human	1	name , trait , alternate_id
156101315	CV2103547	single nucleotide variant	NM_032656.4(DHX37):c.1695C>T (p.Ser565=)	not provided [RCV002927060]	likely benign	12	124965708	124965708	Human		name
156103896	CV2107893	single nucleotide variant	NM_032656.4(DHX37):c.2424G>A (p.Thr808=)	not provided [RCV002927150]	likely benign\|uncertain significance	12	124956720	124956720	Human		name
156237156	CV2108908	single nucleotide variant	NM_032656.4(DHX37):c.1953C>T (p.Gly651=)	not provided [RCV002933065]	likely benign	12	124964486	124964486	Human		name
156134108	CV2113200	single nucleotide variant	NM_032656.4(DHX37):c.1515C>T (p.Asp505=)	not provided [RCV002928313]	likely benign	12	124966868	124966868	Human		name
156025217	CV2128885	single nucleotide variant	NM_032656.4(DHX37):c.1767C>T (p.His589=)	not provided [RCV002948970]	likely benign	12	124964975	124964975	Human		name
156136368	CV2129048	single nucleotide variant	NM_032656.4(DHX37):c.142G>A (p.Ala48Thr)	DHX37-related disorder [RCV003973584]\|not provided [RCV002954063]	benign	12	124986230	124986230	Human	1	name , trait , alternate_id
155977269	CV2132484	single nucleotide variant	NM_032656.4(DHX37):c.2799G>C (p.Leu933=)	not provided [RCV002995918]	likely benign	12	124952467	124952467	Human		name
156019686	CV2141153	single nucleotide variant	NM_032656.4(DHX37):c.2883C>T (p.Asp961=)	not provided [RCV002976091]	likely benign	12	124950790	124950790	Human		name
155911853	CV2148305	single nucleotide variant	NM_032656.4(DHX37):c.1776G>T (p.Pro592=)	not provided [RCV002991379]	likely benign	12	124964966	124964966	Human		name
156290917	CV2156239	single nucleotide variant	NM_032656.4(DHX37):c.1482A>G (p.Pro494=)	not provided [RCV003009965]	likely benign	12	124967145	124967145	Human		name
156220042	CV2173167	single nucleotide variant	NM_032656.4(DHX37):c.2160C>T (p.Val720=)	not provided [RCV003025156]	likely benign	12	124957133	124957133	Human		name
156191879	CV2175255	single nucleotide variant	NM_032656.4(DHX37):c.289C>G (p.Leu97Val)	not provided [RCV003057860]	uncertain significance	12	124982611	124982611	Human		name
156130624	CV2182101	single nucleotide variant	NM_032656.4(DHX37):c.176C>T (p.Thr59Ile)	not provided [RCV003055824]	uncertain significance	12	124986196	124986196	Human		name
156248545	CV2192643	single nucleotide variant	NM_032656.4(DHX37):c.116C>T (p.Thr39Met)	not provided [RCV003059935]	uncertain significance	12	124986256	124986256	Human		name
156253761	CV2284092	single nucleotide variant	NM_032656.4(DHX37):c.112G>C (p.Asp38His)	Inborn genetic diseases [RCV002854996]	uncertain significance	12	124986260	124986260	Human	1	name
401909934	CV2817116	single nucleotide variant	NM_032656.4(DHX37):c.2691C>T (p.Thr897=)	not provided [RCV003398259]	likely benign	12	124953884	124953884	Human		name
401910184	CV2817118	single nucleotide variant	NM_032656.4(DHX37):c.2061G>A (p.Ala687=)	not provided [RCV003398261]	likely benign	12	124960408	124960408	Human		name
401943461	CV2840052	single nucleotide variant	NM_032656.4(DHX37):c.2211C>T (p.Ala737=)	not provided [RCV003456839]	likely benign	12	124957082	124957082	Human		name
405064217	CV2868521	single nucleotide variant	NM_032656.4(DHX37):c.2985C>T (p.Gly995=)	not provided [RCV003548059]	likely benign	12	124950549	124950549	Human		name
405193162	CV2872164	single nucleotide variant	NM_032656.4(DHX37):c.2190C>T (p.Ser730=)	not provided [RCV003550538]	likely benign	12	124957103	124957103	Human		name
405222247	CV2880949	single nucleotide variant	NM_032656.4(DHX37):c.2931C>T (p.Pro977=)	not provided [RCV003554054]	likely benign	12	124950742	124950742	Human		name
405223036	CV2890978	single nucleotide variant	NM_032656.4(DHX37):c.1149C>T (p.Ile383=)	not provided [RCV003554117]	likely benign	12	124971344	124971344	Human		name
405119060	CV2891423	single nucleotide variant	NM_032656.4(DHX37):c.1047G>A (p.Thr349=)	not provided [RCV003558863]	likely benign	12	124972533	124972533	Human		name
405015722	CV2930470	single nucleotide variant	NM_032656.4(DHX37):c.1197C>T (p.Asn399=)	not provided [RCV003577030]	likely benign	12	124968963	124968963	Human		name
402497415	CV2942914	single nucleotide variant	NM_032656.4(DHX37):c.2442G>A (p.Glu814=)	not provided [RCV003661213]	likely benign	12	124956702	124956702	Human		name
405069691	CV2944680	single nucleotide variant	NM_032656.4(DHX37):c.2382C>T (p.His794=)	not provided [RCV003663840]	likely benign	12	124956762	124956762	Human		name
402509279	CV2994594	single nucleotide variant	NM_032656.4(DHX37):c.278G>T (p.Arg93Leu)	not provided [RCV003689393]	uncertain significance	12	124982622	124982622	Human		name
405122198	CV3024635	single nucleotide variant	NM_032656.4(DHX37):c.2784C>T (p.Ile928=)	not provided [RCV003700823]	likely benign	12	124952482	124952482	Human		name
405157856	CV3028113	single nucleotide variant	NM_032656.4(DHX37):c.1908G>A (p.Val636=)	not provided [RCV003703602]	likely benign	12	124964531	124964531	Human		name
405225858	CV3058422	single nucleotide variant	NM_032656.4(DHX37):c.1581G>A (p.Ala527=)	not provided [RCV003733938]	likely benign	12	124966802	124966802	Human		name
405155778	CV3064873	single nucleotide variant	NM_032656.4(DHX37):c.127G>A (p.Val43Ile)	Inborn genetic diseases [RCV004374198]\|not provided [RCV003726737]	uncertain significance	12	124986245	124986245	Human	1	name
405084635	CV3137583	single nucleotide variant	NM_032656.4(DHX37):c.2142G>A (p.Ala714=)	not provided [RCV003834292]	likely benign	12	124960327	124960327	Human		name
405246866	CV3158538	single nucleotide variant	NM_032656.4(DHX37):c.2703C>T (p.Ala901=)	not provided [RCV003868880]	likely benign	12	124952563	124952563	Human		name
405287556	CV3220695	single nucleotide variant	NM_032656.4(DHX37):c.2559C>T (p.Gly853=)	DHX37-related disorder [RCV003959841]	likely benign	12	124954106	124954106	Human		name , trait , alternate_id
405692796	CV3243712	single nucleotide variant	NM_032656.4(DHX37):c.143C>T (p.Ala48Val)	Inborn genetic diseases [RCV004373603]	uncertain significance	12	124986229	124986229	Human	1	name
596924217	CV3532136	single nucleotide variant	NM_032656.4(DHX37):c.1644C>T (p.Gly548=)	not provided [RCV004777247]	uncertain significance	12	124965759	124965759	Human		name
596948034	CV3547626	single nucleotide variant	NM_032656.4(DHX37):c.1113C>T (p.Ile371=)	not provided [RCV004811931]	likely benign	12	124971380	124971380	Human		name
597944607	CV3793766	single nucleotide variant	NM_032656.4(DHX37):c.2964C>T (p.Thr988=)	not provided [RCV005134406]	likely benign	12	124950709	124950709	Human		name
597945428	CV3807336	single nucleotide variant	NM_032656.4(DHX37):c.2244A>G (p.Gln748=)	not provided [RCV005159971]	likely benign	12	124957049	124957049	Human		name
597893474	CV3809925	single nucleotide variant	NM_032656.4(DHX37):c.2349C>G (p.Arg783=)	not provided [RCV005151646]	likely benign	12	124956795	124956795	Human		name
597971499	CV3833076	single nucleotide variant	NM_032656.4(DHX37):c.2178G>A (p.Pro726=)	not provided [RCV005166973]	likely benign	12	124957115	124957115	Human		name
597926855	CV3836846	single nucleotide variant	NM_032656.4(DHX37):c.2337C>T (p.Pro779=)	not provided [RCV005185197]	likely benign	12	124956807	124956807	Human		name
597870767	CV3849210	single nucleotide variant	NM_032656.4(DHX37):c.2031C>T (p.Pro677=)	not provided [RCV005197391]	likely benign	12	124964408	124964408	Human		name
15015036	CV679686	single nucleotide variant	NM_032656.4(DHX37):c.278G>A (p.Arg93Gln)	Intellectual disability [RCV000853098]\|Neurodevelopmental disorder with brain anomalies and with or without vertebral or cardiac anomalies [RCV000991236]\|Neurodevelopmental disorders [RCV001261670]\|not provided [RCV003546607]	pathogenic\|likely pathogenic\|uncertain significance	12	124982622	124982622	Human	5	name
15193745	CV702210	single nucleotide variant	NM_032656.4(DHX37):c.2748G>T (p.Pro916=)	DHX37-related disorder [RCV003926026]\|not provided [RCV000955459]	benign	12	124952518	124952518	Human	1	name , trait , alternate_id
15139175	CV713429	single nucleotide variant	NM_032656.4(DHX37):c.2367A>C (p.Ala789=)	DHX37-related disorder [RCV003916199]\|not provided [RCV000965920]	benign	12	124956777	124956777	Human	1	name , trait , alternate_id
15195472	CV724979	single nucleotide variant	NM_032656.4(DHX37):c.182C>T (p.Ala61Val)	DHX37-related disorder [RCV003940639]\|not provided [RCV000889513]	benign\|likely benign	12	124986190	124986190	Human	1	name , trait , alternate_id
15172770	CV738538	single nucleotide variant	NM_032656.4(DHX37):c.2184C>G (p.Pro728=)	not provided [RCV000905734]	likely benign	12	124957109	124957109	Human		name
21073070	CV792633	single nucleotide variant	NM_032656.4(DHX37):c.1399C>T (p.Leu467=)	Neurodevelopmental disorder with brain anomalies and with or without vertebral or cardiac anomalies [RCV000991234]	pathogenic	12	124968543	124968543	Human	1	name
126725623	CV1017585	single nucleotide variant	NM_032656.4(DHX37):c.985G>A (p.Val329Ile)	46,XY sex reversal 11 [RCV003989681]\|Neurodevelopmental disorder with brain anomalies and with or without vertebral or cardiac anomalies [RCV001331507]\|not provided [RCV002272450]	likely benign\|uncertain significance	12	124972595	124972595	Human	3	name
150453370	CV1203787	single nucleotide variant	NM_032656.4(DHX37):c.769G>A (p.Glu257Lys)	Neurodevelopmental disorder with brain anomalies and with or without vertebral or cardiac anomalies [RCV001591743]	uncertain significance	12	124977460	124977460	Human	1	name
150512382	CV1245416	single nucleotide variant	NM_032656.4(DHX37):c.3195C>T (p.Ala1065=)	46,XY sex reversal 11 [RCV001661400]\|Neurodevelopmental disorder with brain anomalies and with or without vertebral or cardiac anomalies [RCV001661399]\|not provided [RCV001810203]	benign	12	124950170	124950170	Human	3	name
150528388	CV1305852	single nucleotide variant	NM_032656.4(DHX37):c.451C>T (p.Arg151Trp)	46,XY sex reversal 11 [RCV004728801]\|not provided [RCV001755254]	uncertain significance	12	124980777	124980777	Human	2	name
150528714	CV1306048	deletion	NM_032656.4(DHX37):c.2849del (p.Lys950fs)	not provided [RCV001755452]	uncertain significance	12	124952417	124952417	Human		name
153304535	CV1687123	single nucleotide variant	NM_032656.4(DHX37):c.369C>A (p.Asn123Lys)	not provided [RCV002262411]	uncertain significance	12	124982531	124982531	Human		name
153302039	CV1688036	single nucleotide variant	NM_032656.4(DHX37):c.410C>T (p.Ala137Val)	not provided [RCV002265262]	uncertain significance	12	124980818	124980818	Human		name
156272175	CV1899500	single nucleotide variant	NM_032656.4(DHX37):c.3078C>T (p.Cys1026=)	not provided [RCV003086822]	likely benign	12	124950456	124950456	Human		name
156367471	CV1908663	single nucleotide variant	NM_032656.4(DHX37):c.778G>A (p.Val260Ile)	Inborn genetic diseases [RCV004068760]\|not provided [RCV002582167]	uncertain significance	12	124977451	124977451	Human	1	name
156209946	CV1909684	single nucleotide variant	NM_032656.4(DHX37):c.569C>T (p.Ala190Val)	not provided [RCV002596025]	uncertain significance	12	124980659	124980659	Human		name
156364188	CV1932020	single nucleotide variant	NM_032656.4(DHX37):c.515A>T (p.Glu172Val)	not provided [RCV002632889]	uncertain significance	12	124980713	124980713	Human		name
156300538	CV1933453	single nucleotide variant	NM_032656.4(DHX37):c.700G>A (p.Ala234Thr)	not provided [RCV002629224]	likely benign	12	124980528	124980528	Human		name
156445240	CV1945240	single nucleotide variant	NM_032656.4(DHX37):c.448C>T (p.His150Tyr)	Inborn genetic diseases [RCV004245935]\|not provided [RCV003116180]	uncertain significance	12	124980780	124980780	Human	1	name
156251930	CV1984850	single nucleotide variant	NM_032656.4(DHX37):c.3459C>G (p.Pro1153=)	not provided [RCV002645925]	likely benign	12	124947817	124947817	Human		name
155935765	CV2023998	single nucleotide variant	NM_032656.4(DHX37):c.904G>A (p.Gly302Ser)	Inborn genetic diseases [RCV003250580]\|not provided [RCV002774856]	uncertain significance	12	124975495	124975495	Human	1	name
156217862	CV2070749	single nucleotide variant	NM_032656.4(DHX37):c.901A>G (p.Ile301Val)	not provided [RCV002829569]	uncertain significance	12	124975498	124975498	Human		name
156018389	CV2079947	single nucleotide variant	NM_032656.4(DHX37):c.400G>A (p.Glu134Lys)	not provided [RCV002866478]	uncertain significance	12	124980828	124980828	Human		name
156203203	CV2092594	single nucleotide variant	NM_032656.4(DHX37):c.3186G>A (p.Lys1062=)	DHX37-related disorder [RCV003963402]\|not provided [RCV002917864]	likely benign	12	124950179	124950179	Human	1	name , trait , alternate_id
155979151	CV2101490	single nucleotide variant	NM_032656.4(DHX37):c.799G>A (p.Glu267Lys)	DHX37-related disorder [RCV003916559]\|not provided [RCV002907618]	benign	12	124977430	124977430	Human	1	name , trait , alternate_id
156024109	CV2105979	single nucleotide variant	NM_032656.4(DHX37):c.313G>T (p.Ala105Ser)	not provided [RCV002923210]	uncertain significance	12	124982587	124982587	Human		name
156297638	CV2108632	single nucleotide variant	NM_032656.4(DHX37):c.319G>A (p.Glu107Lys)	not provided [RCV002922423]	likely benign	12	124982581	124982581	Human		name
156354666	CV2129047	single nucleotide variant	NM_032656.4(DHX37):c.540C>G (p.Asp180Glu)	DHX37-related disorder [RCV003963493]\|not provided [RCV002966564]	benign	12	124980688	124980688	Human	1	name , trait , alternate_id
155933309	CV2129304	single nucleotide variant	NM_032656.4(DHX37):c.3081C>T (p.Pro1027=)	not provided [RCV002970756]	likely benign	12	124950453	124950453	Human		name
156220387	CV2144094	single nucleotide variant	NM_032656.4(DHX37):c.3306G>A (p.Thr1102=)	not provided [RCV003007356]	likely benign	12	124948166	124948166	Human		name
156223233	CV2144309	single nucleotide variant	NM_032656.4(DHX37):c.979C>T (p.Arg327Trp)	not provided [RCV003007463]	uncertain significance	12	124975420	124975420	Human		name
156349284	CV2146904	single nucleotide variant	NM_032656.4(DHX37):c.3084G>A (p.Glu1028=)	not provided [RCV003030747]	likely benign	12	124950450	124950450	Human		name
156033684	CV2275149	single nucleotide variant	NM_032656.4(DHX37):c.916C>G (p.Pro306Ala)	Inborn genetic diseases [RCV002845572]	uncertain significance	12	124975483	124975483	Human	1	name
156098876	CV2306498	single nucleotide variant	NM_032656.4(DHX37):c.403G>T (p.Val135Leu)	Inborn genetic diseases [RCV002888501]	uncertain significance	12	124980825	124980825	Human	1	name
243049461	CV2416831	single nucleotide variant	NM_032656.4(DHX37):c.461G>A (p.Arg154His)	Inborn genetic diseases [RCV003294652]\|not provided [RCV005099422]\|not specified [RCV003151503]	likely benign\|uncertain significance	12	124980767	124980767	Human	1	name
329367281	CV2427335	single nucleotide variant	NM_032656.4(DHX37):c.628G>A (p.Val210Met)	Inborn genetic diseases [RCV003183152]\|not provided [RCV003565627]	uncertain significance	12	124980600	124980600	Human	1	name
329401872	CV2457962	single nucleotide variant	NM_032656.4(DHX37):c.643A>G (p.Thr215Ala)	Inborn genetic diseases [RCV003198913]	uncertain significance	12	124980585	124980585	Human	1	name
329401873	CV2457963	single nucleotide variant	NM_032656.4(DHX37):c.828G>C (p.Glu276Asp)	Inborn genetic diseases [RCV003198914]	uncertain significance	12	124977401	124977401	Human	1	name
329396653	CV2459793	single nucleotide variant	NM_032656.4(DHX37):c.655C>T (p.Pro219Ser)	Inborn genetic diseases [RCV003219658]	uncertain significance	12	124980573	124980573	Human	1	name
329387685	CV2470897	single nucleotide variant	NM_032656.4(DHX37):c.811G>C (p.Val271Leu)	Inborn genetic diseases [RCV003215384]	uncertain significance	12	124977418	124977418	Human	1	name
401780303	CV2725983	single nucleotide variant	NM_032656.4(DHX37):c.442G>T (p.Gly148Cys)	Inborn genetic diseases [RCV003287956]	uncertain significance	12	124980786	124980786	Human	1	name
401861699	CV2756427	single nucleotide variant	NM_032656.4(DHX37):c.370C>T (p.Arg124Cys)	Inborn genetic diseases [RCV003342767]	uncertain significance	12	124982530	124982530	Human	1	name
401934100	CV2817120	single nucleotide variant	NM_032656.4(DHX37):c.932C>T (p.Ala311Val)	not provided [RCV003410959]	uncertain significance	12	124975467	124975467	Human		name
401909942	CV2817122	single nucleotide variant	NM_032656.4(DHX37):c.703G>A (p.Val235Ile)	Inborn genetic diseases [RCV004364514]\|not provided [RCV003398263]	likely benign\|uncertain significance	12	124980525	124980525	Human	1	name
405718662	CV2852018	duplication	NM_032656.4(DHX37):c.2177dup (p.Thr727fs)	Male infertility with azoospermia or oligozoospermia due to single gene mutation [RCV003991646]	likely pathogenic	12	124957115	124957116	Human	1	name
405075192	CV2873231	single nucleotide variant	NM_032656.4(DHX37):c.640A>G (p.Met214Val)	not provided [RCV003548771]	uncertain significance	12	124980588	124980588	Human		name
405079283	CV2945447	single nucleotide variant	NM_032656.4(DHX37):c.968A>G (p.Asn323Ser)	not provided [RCV003664465]	uncertain significance	12	124975431	124975431	Human		name
405120912	CV3027109	single nucleotide variant	NM_032656.4(DHX37):c.3150C>T (p.Ile1050=)	not provided [RCV003700667]	likely benign	12	124950215	124950215	Human		name
405178331	CV3027550	single nucleotide variant	NM_032656.4(DHX37):c.650C>G (p.Pro217Arg)	not provided [RCV003705294]	uncertain significance	12	124980578	124980578	Human		name
405093927	CV3045629	single nucleotide variant	NM_032656.4(DHX37):c.586G>A (p.Val196Met)	not provided [RCV003718020]	uncertain significance	12	124980642	124980642	Human		name
405087700	CV3047913	single nucleotide variant	NM_032656.4(DHX37):c.311A>G (p.Gln104Arg)	Inborn genetic diseases [RCV004980965]\|not provided [RCV003717591]	uncertain significance	12	124982589	124982589	Human	1	name
405136557	CV3052219	single nucleotide variant	NM_032656.4(DHX37):c.955G>A (p.Ala319Thr)	not provided [RCV003725262]	uncertain significance	12	124975444	124975444	Human		name
405128789	CV3054423	single nucleotide variant	NM_032656.4(DHX37):c.488A>G (p.Glu163Gly)	not provided [RCV003724632]	uncertain significance	12	124980740	124980740	Human		name
405037775	CV3067630	single nucleotide variant	NM_032656.4(DHX37):c.377A>G (p.Tyr126Cys)	not provided [RCV003739671]	uncertain significance	12	124982523	124982523	Human		name
405115556	CV3115505	single nucleotide variant	NM_032656.4(DHX37):c.3327G>C (p.Leu1109=)	not provided [RCV003814187]	likely benign	12	124948145	124948145	Human		name
405251673	CV3181333	single nucleotide variant	NM_032656.4(DHX37):c.392A>T (p.Lys131Met)	not provided [RCV003870335]	uncertain significance	12	124980836	124980836	Human		name
405695221	CV3226604	single nucleotide variant	NM_032656.4(DHX37):c.399C>G (p.Asp133Glu)	not provided [RCV003992997]	uncertain significance	12	124980829	124980829	Human		name
405692848	CV3243722	single nucleotide variant	NM_032656.4(DHX37):c.683G>C (p.Arg228Thr)	Inborn genetic diseases [RCV004373613]	uncertain significance	12	124980545	124980545	Human	1	name
405692854	CV3243723	single nucleotide variant	NM_032656.4(DHX37):c.920G>A (p.Arg307His)	Inborn genetic diseases [RCV004373614]	uncertain significance	12	124975479	124975479	Human	1	name
405692858	CV3243724	single nucleotide variant	NM_032656.4(DHX37):c.952G>A (p.Val318Met)	Inborn genetic diseases [RCV004373615]	uncertain significance	12	124975447	124975447	Human	1	name
407467474	CV3434162	single nucleotide variant	NM_032656.4(DHX37):c.503A>G (p.Glu168Gly)	Inborn genetic diseases [RCV004614223]	uncertain significance	12	124980725	124980725	Human	1	name
407467477	CV3434163	single nucleotide variant	NM_032656.4(DHX37):c.460C>T (p.Arg154Cys)	Inborn genetic diseases [RCV004614224]	uncertain significance	12	124980768	124980768	Human	1	name
596925450	CV3535787	single nucleotide variant	NM_032656.4(DHX37):c.994C>G (p.Gln332Glu)	46,XY sex reversal 11 [RCV004788217]	uncertain significance	12	124972586	124972586	Human	2	name
596945633	CV3547971	single nucleotide variant	NM_032656.4(DHX37):c.3126C>T (p.Arg1042=)	not provided [RCV004809302]	likely benign	12	124950239	124950239	Human		name
597658097	CV3652408	single nucleotide variant	NM_032656.4(DHX37):c.950G>A (p.Arg317Gln)	Inborn genetic diseases [RCV004976845]	uncertain significance	12	124975449	124975449	Human	1	name
597658122	CV3652414	single nucleotide variant	NM_032656.4(DHX37):c.897C>A (p.Ser299Arg)	Inborn genetic diseases [RCV004976850]	uncertain significance	12	124975502	124975502	Human	1	name
597658128	CV3652415	single nucleotide variant	NM_032656.4(DHX37):c.969T>A (p.Asn323Lys)	Inborn genetic diseases [RCV004976851]\|not provided [RCV005110177]	uncertain significance	12	124975430	124975430	Human	1	name
597658149	CV3652419	single nucleotide variant	NM_032656.4(DHX37):c.560C>T (p.Pro187Leu)	Inborn genetic diseases [RCV004976855]	likely benign	12	124980668	124980668	Human	1	name
597658164	CV3652422	single nucleotide variant	NM_032656.4(DHX37):c.983T>A (p.Val328Asp)	Inborn genetic diseases [RCV004976858]	uncertain significance	12	124972597	124972597	Human	1	name
597658170	CV3652423	single nucleotide variant	NM_032656.4(DHX37):c.724T>A (p.Ser242Thr)	Inborn genetic diseases [RCV004976859]	likely benign	12	124980504	124980504	Human	1	name
597926886	CV3778552	single nucleotide variant	NM_032656.4(DHX37):c.533A>G (p.Glu178Gly)	not provided [RCV005131075]	uncertain significance	12	124980695	124980695	Human		name
597939532	CV3788560	single nucleotide variant	NM_032656.4(DHX37):c.632C>T (p.Pro211Leu)	not provided [RCV005133235]	likely benign	12	124980596	124980596	Human		name
597857380	CV3816738	single nucleotide variant	NM_032656.4(DHX37):c.416G>T (p.Gly139Val)	not provided [RCV005146311]	uncertain significance	12	124980812	124980812	Human		name
597940997	CV3819173	single nucleotide variant	NM_032656.4(DHX37):c.970C>A (p.Leu324Met)	not provided [RCV005158984]	uncertain significance	12	124975429	124975429	Human		name
597873927	CV3849955	single nucleotide variant	NM_032656.4(DHX37):c.3138G>T (p.Pro1046=)	not provided [RCV005197944]	likely benign	12	124950227	124950227	Human		name
598216640	CV3895224	single nucleotide variant	NM_032656.4(DHX37):c.413C>T (p.Pro138Leu)	Neurodevelopmental disorder with brain anomalies and with or without vertebral or cardiac anomalies [RCV005360128]	uncertain significance	12	124980815	124980815	Human	1	name
598171523	CV3953188	single nucleotide variant	NM_032656.4(DHX37):c.619A>T (p.Ser207Cys)	Inborn genetic diseases [RCV005331197]	likely benign	12	124980609	124980609	Human	1	name
598171531	CV3953190	single nucleotide variant	NM_032656.4(DHX37):c.814A>G (p.Ile272Val)	Inborn genetic diseases [RCV005331199]	uncertain significance	12	124977415	124977415	Human	1	name
15199824	CV702211	single nucleotide variant	NM_032656.4(DHX37):c.665C>G (p.Ala222Gly)	DHX37-related disorder [RCV003960681]\|not provided [RCV000957151]	benign	12	124980563	124980563	Human	1	name , trait , alternate_id
15171206	CV702212	single nucleotide variant	NM_032656.4(DHX37):c.506C>T (p.Ser169Leu)	not provided [RCV000949790]	benign	12	124980722	124980722	Human		name
26902598	CV857634	single nucleotide variant	NM_032656.4(DHX37):c.911C>T (p.Thr304Met)	46,XY sex reversal 11 [RCV001089509]	pathogenic	12	124975488	124975488	Human	2	name
26902602	CV857635	single nucleotide variant	NM_032656.4(DHX37):c.923G>A (p.Arg308Gln)	46,XY sex reversal 11 [RCV001089510]\|DHX37-related disorder [RCV004579568]\|not provided [RCV001840781]	pathogenic	12	124975476	124975476	Human	3	name , trait , alternate_id
126725619	CV1017584	single nucleotide variant	NM_032656.4(DHX37):c.2956G>A (p.Val986Met)	46,XY sex reversal 11 [RCV003989680]\|Neurodevelopmental disorder with brain anomalies and with or without vertebral or cardiac anomalies [RCV001331505]\|not provided [RCV002546486]	uncertain significance	12	124950717	124950717	Human	3	name
150337598	CV1166043	single nucleotide variant	NM_032656.4(DHX37):c.2227G>A (p.Ala743Thr)	not provided [RCV001532725]	uncertain significance	12	124957066	124957066	Human		name
150512391	CV1245420	single nucleotide variant	NM_032656.4(DHX37):c.2605A>G (p.Ser869Gly)	46,XY sex reversal 11 [RCV001661408]\|Neurodevelopmental disorder with brain anomalies and with or without vertebral or cardiac anomalies [RCV001661407]\|not provided [RCV002538556]	benign	12	124953970	124953970	Human	3	name
150529862	CV1288222	single nucleotide variant	NM_032656.4(DHX37):c.1877C>T (p.Ser626Leu)	46,XY sex reversal 11 [RCV001726690]	likely pathogenic	12	124964562	124964562	Human	2	name
150552643	CV1308368	single nucleotide variant	NM_032656.4(DHX37):c.2984G>C (p.Gly995Ala)	not provided [RCV001768208]	uncertain significance	12	124950550	124950550	Human		name
152978541	CV1671708	single nucleotide variant	NM_032656.4(DHX37):c.1706T>A (p.Leu569Gln)	Inborn genetic diseases [RCV004047255]\|Neurodevelopmental disorder with brain anomalies and with or without vertebral or cardiac anomalies [RCV002227813]	uncertain significance	12	124965697	124965697	Human	2	name
152978543	CV1671709	single nucleotide variant	NM_032656.4(DHX37):c.1288A>T (p.Ile430Phe)	Neurodevelopmental disorder with brain anomalies and with or without vertebral or cardiac anomalies [RCV002227814]\|not provided [RCV004591849]	uncertain significance	12	124968872	124968872	Human	1	name
153347021	CV1691914	single nucleotide variant	NM_032656.4(DHX37):c.1270G>A (p.Ala424Thr)	not provided [RCV002273397]	conflicting interpretations of pathogenicity\|uncertain significance	12	124968890	124968890	Human		name
153349339	CV1693122	single nucleotide variant	NM_032656.4(DHX37):c.1582C>T (p.Arg528Trp)	not provided [RCV002275740]	uncertain significance	12	124966801	124966801	Human		name
153349002	CV1693123	single nucleotide variant	NM_032656.4(DHX37):c.1544G>A (p.Arg515Gln)	Inborn genetic diseases [RCV004973394]\|not provided [RCV002275385]	uncertain significance	12	124966839	124966839	Human	1	name
155645870	CV1709226	single nucleotide variant	NM_032656.4(DHX37):c.2905A>G (p.Ser969Gly)	not provided [RCV002292102]	uncertain significance	12	124950768	124950768	Human		name
156409007	CV1880038	single nucleotide variant	NM_032656.4(DHX37):c.1090C>A (p.Leu364Met)	not provided [RCV003071494]	uncertain significance	12	124971403	124971403	Human		name
156409073	CV1880086	single nucleotide variant	NM_032656.4(DHX37):c.2713G>A (p.Glu905Lys)	Inborn genetic diseases [RCV004070375]\|Neurodevelopmental disorder with brain anomalies and with or without vertebral or cardiac anomalies [RCV004725502]\|not provided [RCV003071519]	likely benign\|uncertain significance	12	124952553	124952553	Human	2	name
156358668	CV1904125	single nucleotide variant	NM_032656.4(DHX37):c.1464G>C (p.Arg488Ser)	Neurodevelopmental disorder with brain anomalies and with or without vertebral or cardiac anomalies [RCV004725531]\|not provided [RCV002581572]	likely benign\|uncertain significance	12	124967163	124967163	Human	1	name
156407917	CV1911377	single nucleotide variant	NM_032656.4(DHX37):c.2911G>A (p.Val971Ile)	DHX37-related disorder [RCV003410120]\|not provided [RCV002607051]	uncertain significance	12	124950762	124950762	Human	1	name , trait , alternate_id
155960091	CV1912050	single nucleotide variant	NM_032656.4(DHX37):c.2396A>G (p.Tyr799Cys)	Inborn genetic diseases [RCV003274283]\|not provided [RCV002616689]	uncertain significance	12	124956748	124956748	Human	1	name
155952757	CV1918191	single nucleotide variant	NM_032656.4(DHX37):c.1954G>A (p.Val652Ile)	not provided [RCV002616312]	uncertain significance	12	124964485	124964485	Human		name
156099662	CV1920653	single nucleotide variant	NM_032656.4(DHX37):c.2417G>A (p.Ser806Asn)	Neurodevelopmental disorder with brain anomalies and with or without vertebral or cardiac anomalies [RCV005363034]\|not provided [RCV002592227]	uncertain significance	12	124956727	124956727	Human	1	name
156409907	CV1922956	single nucleotide variant	NM_032656.4(DHX37):c.1394G>A (p.Arg465Gln)	not provided [RCV002607699]	uncertain significance	12	124968548	124968548	Human		name
156157753	CV1928273	single nucleotide variant	NM_032656.4(DHX37):c.1496G>A (p.Arg499Gln)	Inborn genetic diseases [RCV002648087]\|not provided [RCV002664127]	uncertain significance	12	124967131	124967131	Human	1	name
156375906	CV1930470	single nucleotide variant	NM_032656.4(DHX37):c.2497C>T (p.Arg833Trp)	not provided [RCV002633829]	uncertain significance	12	124954168	124954168	Human		name
156363442	CV1931925	single nucleotide variant	NM_032656.4(DHX37):c.2498G>A (p.Arg833Gln)	Inborn genetic diseases [RCV002632840]\|not provided [RCV002632839]	uncertain significance	12	124954167	124954167	Human	1	name
156444055	CV1937573	single nucleotide variant	NM_032656.4(DHX37):c.1405G>A (p.Ala469Thr)	not provided [RCV003114973]	uncertain significance	12	124968537	124968537	Human		name
156442463	CV1938752	single nucleotide variant	NM_032656.4(DHX37):c.1511A>G (p.Asp504Gly)	Inborn genetic diseases [RCV003162163]\|not provided [RCV003112808]	uncertain significance	12	124966872	124966872	Human	1	name
156444595	CV1948324	single nucleotide variant	NM_032656.4(DHX37):c.2246C>T (p.Pro749Leu)	not provided [RCV003115519]	uncertain significance	12	124957047	124957047	Human		name
156254856	CV1960708	single nucleotide variant	NM_032656.4(DHX37):c.1015G>T (p.Val339Leu)	Inborn genetic diseases [RCV003164794]\|not provided [RCV002576656]	uncertain significance	12	124972565	124972565	Human	1	name
156171115	CV1968324	single nucleotide variant	NM_032656.4(DHX37):c.2389C>G (p.Leu797Val)	Inborn genetic diseases [RCV005333276]\|not provided [RCV002594773]	uncertain significance	12	124956755	124956755	Human	1	name
156254158	CV2025870	single nucleotide variant	NM_032656.4(DHX37):c.2955C>G (p.Ile985Met)	not provided [RCV002746093]	uncertain significance	12	124950718	124950718	Human		name
155906114	CV2027597	single nucleotide variant	NM_032656.4(DHX37):c.1577A>G (p.Lys526Arg)	Inborn genetic diseases [RCV004973583]\|not provided [RCV002726480]	uncertain significance	12	124966806	124966806	Human	1	name
155918249	CV2030093	single nucleotide variant	NM_032656.4(DHX37):c.2318G>A (p.Arg773Gln)	not provided [RCV002750575]	uncertain significance	12	124956826	124956826	Human		name
156115860	CV2035527	single nucleotide variant	NM_032656.4(DHX37):c.2668C>T (p.Arg890Cys)	Inborn genetic diseases [RCV004064652]\|not provided [RCV002785589]	uncertain significance	12	124953907	124953907	Human	1	name
156162178	CV2044920	single nucleotide variant	NM_032656.4(DHX37):c.1474G>C (p.Ala492Pro)	not provided [RCV002741585]	uncertain significance	12	124967153	124967153	Human		name
156374354	CV2049078	single nucleotide variant	NM_032656.4(DHX37):c.1823C>T (p.Pro608Leu)	not provided [RCV002814565]	uncertain significance	12	124964616	124964616	Human		name
156234849	CV2056232	single nucleotide variant	NM_032656.4(DHX37):c.1169G>A (p.Arg390His)	not provided [RCV002791133]	uncertain significance	12	124971324	124971324	Human		name
155990993	CV2066804	single nucleotide variant	NM_032656.4(DHX37):c.2781G>C (p.Gln927His)	not provided [RCV002842957]	uncertain significance	12	124952485	124952485	Human		name
156044025	CV2071812	single nucleotide variant	NM_032656.4(DHX37):c.2109G>C (p.Arg703Ser)	not provided [RCV002846208]	uncertain significance	12	124960360	124960360	Human		name
156146926	CV2078727	single nucleotide variant	NM_032656.4(DHX37):c.2037C>G (p.His679Gln)	not provided [RCV002872186]	uncertain significance	12	124964402	124964402	Human		name
156010989	CV2079733	single nucleotide variant	NM_032656.4(DHX37):c.1373G>A (p.Arg458Gln)	not provided [RCV002866107]	benign	12	124968569	124968569	Human		name
156225855	CV2081098	single nucleotide variant	NM_032656.4(DHX37):c.1796C>G (p.Pro599Arg)	not provided [RCV002853385]	uncertain significance	12	124964946	124964946	Human		name
155987030	CV2091267	single nucleotide variant	NM_032656.4(DHX37):c.1451C>T (p.Ala484Val)	not provided [RCV002907974]	likely benign	12	124967176	124967176	Human	6	name
156204825	CV2092670	single nucleotide variant	NM_032656.4(DHX37):c.2162T>C (p.Ile721Thr)	Inborn genetic diseases [RCV003167917]\|not provided [RCV002917922]	uncertain significance	12	124957131	124957131	Human	1	name
156025345	CV2106075	single nucleotide variant	NM_032656.4(DHX37):c.1405G>T (p.Ala469Ser)	46,XY sex reversal 11 [RCV005010793]\|Inborn genetic diseases [RCV002923262]\|not provided [RCV002923263]	uncertain significance	12	124968537	124968537	Human	4	name
155995919	CV2109360	single nucleotide variant	NM_032656.4(DHX37):c.2429G>A (p.Arg810Gln)	DHX37-related disorder [RCV003906346]\|not provided [RCV002947559]	benign	12	124956715	124956715	Human	1	name , trait , alternate_id
156023198	CV2111202	single nucleotide variant	NM_032656.4(DHX37):c.2995G>A (p.Val999Met)	DHX37-related disorder [RCV003926519]\|not provided [RCV002909712]	likely benign\|conflicting interpretations of pathogenicity	12	124950539	124950539	Human	1	name , trait , alternate_id
156309618	CV2111204	single nucleotide variant	NM_032656.4(DHX37):c.2149G>A (p.Val717Ile)	DHX37-related disorder [RCV003936373]\|not provided [RCV002937088]	benign	12	124960320	124960320	Human	1	name , trait , alternate_id
156025412	CV2112439	single nucleotide variant	NM_032656.4(DHX37):c.1696G>A (p.Asp566Asn)	not provided [RCV002909813]	benign	12	124965707	124965707	Human		name
156025837	CV2112518	single nucleotide variant	NM_032656.4(DHX37):c.2288G>A (p.Arg763Gln)	Inborn genetic diseases [RCV002909833]\|not provided [RCV002928149]	uncertain significance	12	124956856	124956856	Human	1	name
156142083	CV2113060	single nucleotide variant	NM_032656.4(DHX37):c.1973C>T (p.Thr658Ile)	Inborn genetic diseases [RCV005333392]\|not provided [RCV002914946]	uncertain significance	12	124964466	124964466	Human	1	name
156142741	CV2113145	single nucleotide variant	NM_032656.4(DHX37):c.1277C>T (p.Pro426Leu)	not provided [RCV002914967]	uncertain significance	12	124968883	124968883	Human		name
156102752	CV2117293	single nucleotide variant	NM_032656.4(DHX37):c.2104C>T (p.Arg702Trp)	not provided [RCV002952799]	uncertain significance	12	124960365	124960365	Human		name
156343625	CV2124098	single nucleotide variant	NM_032656.4(DHX37):c.1745C>T (p.Pro582Leu)	Inborn genetic diseases [RCV002939039]\|not provided [RCV002942699]	uncertain significance	12	124964997	124964997	Human	1	name
156009017	CV2124448	single nucleotide variant	NM_032656.4(DHX37):c.1583G>A (p.Arg528Gln)	Inborn genetic diseases [RCV004067309]\|not provided [RCV002948160]	likely benign	12	124966800	124966800	Human	1	name
156243926	CV2126225	single nucleotide variant	NM_032656.4(DHX37):c.1585G>A (p.Ala529Thr)	Inborn genetic diseases [RCV004068221]\|not provided [RCV002958969]	likely benign\|uncertain significance	12	124966798	124966798	Human	1	name
156273902	CV2132946	single nucleotide variant	NM_032656.4(DHX37):c.2348G>A (p.Arg783His)	not provided [RCV003009363]	uncertain significance	12	124956796	124956796	Human		name
155960993	CV2138375	single nucleotide variant	NM_032656.4(DHX37):c.1292A>G (p.Lys431Arg)	Inborn genetic diseases [RCV002972384]\|not provided [RCV002979351]	likely benign\|uncertain significance	12	124968868	124968868	Human	1	name
156317415	CV2140427	single nucleotide variant	NM_032656.4(DHX37):c.1631C>T (p.Pro544Leu)	DHX37-related disorder [RCV004750242]\|Inborn genetic diseases [RCV004978460]\|not provided [RCV003011473]	uncertain significance	12	124965772	124965772	Human	2	name , trait , alternate_id
155957674	CV2141900	single nucleotide variant	NM_032656.4(DHX37):c.2060C>T (p.Ala687Val)	Inborn genetic diseases [RCV003170781]\|not provided [RCV002972216]	uncertain significance	12	124960409	124960409	Human	1	name
156033341	CV2142268	single nucleotide variant	NM_032656.4(DHX37):c.2584G>A (p.Val862Met)	Inborn genetic diseases [RCV005333410]\|not provided [RCV002976699]	uncertain significance	12	124953991	124953991	Human	1	name
156247438	CV2145608	single nucleotide variant	NM_032656.4(DHX37):c.1495C>G (p.Arg499Gly)	not provided [RCV003008321]	uncertain significance	12	124967132	124967132	Human		name
155935534	CV2149827	single nucleotide variant	NM_032656.4(DHX37):c.1061T>G (p.Leu354Arg)	not provided [RCV003013910]	uncertain significance	12	124972519	124972519	Human		name
156316017	CV2158743	single nucleotide variant	NM_032656.4(DHX37):c.1702G>A (p.Asp568Asn)	not provided [RCV003028864]	uncertain significance	12	124965701	124965701	Human		name
155999057	CV2168944	single nucleotide variant	NM_032656.4(DHX37):c.2147A>G (p.Asn716Ser)	Inborn genetic diseases [RCV003017186]\|not provided [RCV003026285]	uncertain significance	12	124960322	124960322	Human	1	name
156128127	CV2184847	single nucleotide variant	NM_032656.4(DHX37):c.2757G>C (p.Glu919Asp)	not provided [RCV003039588]	uncertain significance	12	124952509	124952509	Human		name
156056309	CV2192733	single nucleotide variant	NM_032656.4(DHX37):c.2581G>A (p.Ala861Thr)	not provided [RCV003037090]	uncertain significance	12	124953994	124953994	Human		name
156247859	CV2202980	single nucleotide variant	NM_032656.4(DHX37):c.2642G>A (p.Arg881Gln)	Inborn genetic diseases [RCV002668195]\|not provided [RCV003561065]	uncertain significance	12	124953933	124953933	Human	1	name
156226062	CV2203100	single nucleotide variant	NM_032656.4(DHX37):c.2228C>G (p.Ala743Gly)	Inborn genetic diseases [RCV002644638]	uncertain significance	12	124957065	124957065	Human	1	name
156130734	CV2210090	single nucleotide variant	NM_032656.4(DHX37):c.2816G>A (p.Arg939His)	Inborn genetic diseases [RCV002696433]\|not provided [RCV003546869]	uncertain significance	12	124952450	124952450	Human	1	name
156094202	CV2213310	single nucleotide variant	NM_032656.4(DHX37):c.1346T>G (p.Leu449Arg)	Inborn genetic diseases [RCV002661541]	uncertain significance	12	124968596	124968596	Human	1	name
156234277	CV2223948	single nucleotide variant	NM_032656.4(DHX37):c.2105G>A (p.Arg702Gln)	Inborn genetic diseases [RCV002712964]	uncertain significance	12	124960364	124960364	Human	1	name
155928814	CV2224439	single nucleotide variant	NM_032656.4(DHX37):c.1941C>A (p.Asp647Glu)	Inborn genetic diseases [RCV002728465]	uncertain significance	12	124964498	124964498	Human	1	name
155928825	CV2224440	single nucleotide variant	NM_032656.4(DHX37):c.1942C>A (p.Arg648Ser)	Inborn genetic diseases [RCV002728466]	uncertain significance	12	124964497	124964497	Human	1	name
155987065	CV2234057	single nucleotide variant	NM_032656.4(DHX37):c.1283C>T (p.Pro428Leu)	Inborn genetic diseases [RCV002732975]	uncertain significance	12	124968877	124968877	Human	1	name
155974876	CV2235781	single nucleotide variant	NM_032656.4(DHX37):c.1531G>C (p.Val511Leu)	Inborn genetic diseases [RCV002777178]	uncertain significance	12	124966852	124966852	Human	1	name
155968088	CV2261954	single nucleotide variant	NM_032656.4(DHX37):c.1943G>A (p.Arg648His)	Inborn genetic diseases [RCV002817452]	uncertain significance	12	124964496	124964496	Human	1	name
156162064	CV2311786	single nucleotide variant	NM_032656.4(DHX37):c.2298C>G (p.Cys766Trp)	Inborn genetic diseases [RCV002916049]\|not provided [RCV005099841]	uncertain significance	12	124956846	124956846	Human	1	name
156348009	CV2312536	single nucleotide variant	NM_032656.4(DHX37):c.2815C>T (p.Arg939Cys)	Inborn genetic diseases [RCV002939433]\|Neurodevelopmental disorder with brain anomalies and with or without vertebral or cardiac anomalies [RCV005363056]	uncertain significance	12	124952451	124952451	Human	2	name
156084057	CV2330805	single nucleotide variant	NM_032656.4(DHX37):c.2375G>A (p.Arg792Gln)	Inborn genetic diseases [RCV002926340]\|not provided [RCV003546920]	likely benign\|uncertain significance	12	124956769	124956769	Human	1	name
155973566	CV2334453	single nucleotide variant	NM_032656.4(DHX37):c.1681G>A (p.Gly561Arg)	Inborn genetic diseases [RCV002946013]\|not provided [RCV003456558]	uncertain significance	12	124965722	124965722	Human	1	name
156152125	CV2369238	single nucleotide variant	NM_032656.4(DHX37):c.1261C>T (p.Arg421Trp)	Inborn genetic diseases [RCV003004615]	uncertain significance	12	124968899	124968899	Human	1	name
156177665	CV2374536	single nucleotide variant	NM_032656.4(DHX37):c.2669G>A (p.Arg890His)	Inborn genetic diseases [RCV002699188]	uncertain significance	12	124953906	124953906	Human	1	name
156109812	CV2390420	single nucleotide variant	NM_032656.4(DHX37):c.2666G>A (p.Arg889Gln)	Inborn genetic diseases [RCV002739631]\|Neurodevelopmental disorder with brain anomalies and with or without vertebral or cardiac anomalies [RCV004786869]\|not provided [RCV005099171]	uncertain significance	12	124953909	124953909	Human	2	name
243051309	CV2415758	single nucleotide variant	NM_032656.4(DHX37):c.2221T>A (p.Leu741Met)	Neurodevelopmental disorder with brain anomalies and with or without vertebral or cardiac anomalies [RCV003148367]	uncertain significance	12	124957072	124957072	Human	1	name
243052647	CV2416194	single nucleotide variant	NM_032656.4(DHX37):c.1355A>G (p.Tyr452Cys)	not provided [RCV003149255]	uncertain significance	12	124968587	124968587	Human		name
243053853	CV2416420	single nucleotide variant	NM_032656.4(DHX37):c.1372C>T (p.Arg458Trp)	Neurodevelopmental disorder with brain anomalies and with or without vertebral or cardiac anomalies [RCV005356367]\|not provided [RCV003149481]	uncertain significance	12	124968570	124968570	Human	1	name
401737026	CV2679208	single nucleotide variant	NM_032656.4(DHX37):c.2338G>A (p.Val780Met)	Inborn genetic diseases [RCV003239744]	uncertain significance	12	124956806	124956806	Human	1	name
401782379	CV2686774	single nucleotide variant	NM_032656.4(DHX37):c.1343C>T (p.Pro448Leu)	Inborn genetic diseases [RCV003265718]	uncertain significance	12	124968599	124968599	Human	1	name
401750484	CV2715655	single nucleotide variant	NM_032656.4(DHX37):c.2486T>C (p.Leu829Pro)	Inborn genetic diseases [RCV003295195]	uncertain significance	12	124954179	124954179	Human	1	name
401728600	CV2729684	single nucleotide variant	NM_032656.4(DHX37):c.1611G>C (p.Leu537Phe)	Inborn genetic diseases [RCV003288645]	uncertain significance	12	124965792	124965792	Human	1	name
401865608	CV2749290	single nucleotide variant	NM_032656.4(DHX37):c.1150C>G (p.Leu384Val)	Inborn genetic diseases [RCV004334110]\|not specified [RCV003330488]	uncertain significance	12	124971343	124971343	Human	1	name
401863068	CV2765901	single nucleotide variant	NM_032656.4(DHX37):c.2626G>A (p.Glu876Lys)	Inborn genetic diseases [RCV003378301]	uncertain significance	12	124953949	124953949	Human	1	name
401882500	CV2778245	single nucleotide variant	NM_032656.4(DHX37):c.1336C>T (p.Arg446Trp)	Inborn genetic diseases [RCV003350448]	uncertain significance	12	124968606	124968606	Human	1	name
401910182	CV2817117	single nucleotide variant	NM_032656.4(DHX37):c.2504G>A (p.Arg835Gln)	not provided [RCV003398260]	uncertain significance	12	124954161	124954161	Human		name
401909940	CV2817119	single nucleotide variant	NM_032656.4(DHX37):c.1105G>A (p.Val369Met)	not provided [RCV003398262]	uncertain significance	12	124971388	124971388	Human		name
405718489	CV2851975	single nucleotide variant	NM_032656.4(DHX37):c.2762A>G (p.Gln921Arg)	Male infertility with azoospermia or oligozoospermia due to single gene mutation [RCV003991603]	likely pathogenic	12	124952504	124952504	Human	1	name
405718579	CV2852008	single nucleotide variant	NM_032656.4(DHX37):c.1156G>A (p.Gly386Ser)	Male infertility with spermatogenesis disorder [RCV003991636]\|not provided [RCV005235719]	likely pathogenic\|uncertain significance	12	124971337	124971337	Human	1	name
405718625	CV2852019	single nucleotide variant	NM_032656.4(DHX37):c.2698A>G (p.Asn900Asp)	Male infertility with azoospermia or oligozoospermia due to single gene mutation [RCV003991647]	likely pathogenic	12	124952568	124952568	Human	1	name
405239279	CV2889177	single nucleotide variant	NM_032656.4(DHX37):c.2674C>T (p.Arg892Trp)	not provided [RCV003556908]	uncertain significance	12	124953901	124953901	Human		name
402464747	CV2916420	single nucleotide variant	NM_032656.4(DHX37):c.1513G>A (p.Asp505Asn)	Inborn genetic diseases [RCV004980887]\|not provided [RCV003569086]	uncertain significance	12	124966870	124966870	Human	1	name
405223412	CV2919091	single nucleotide variant	NM_032656.4(DHX37):c.1920G>C (p.Lys640Asn)	not provided [RCV003568774]	uncertain significance	12	124964519	124964519	Human		name
405183766	CV2920296	single nucleotide variant	NM_032656.4(DHX37):c.2335C>T (p.Pro779Ser)	not provided [RCV003564250]	uncertain significance	12	124956809	124956809	Human		name
405072736	CV2940495	single nucleotide variant	NM_032656.4(DHX37):c.2459C>T (p.Ala820Val)	not provided [RCV003659518]	uncertain significance	12	124954206	124954206	Human		name
402496498	CV2942850	single nucleotide variant	NM_032656.4(DHX37):c.2830G>A (p.Glu944Lys)	Inborn genetic diseases [RCV004371494]\|not provided [RCV003661183]	uncertain significance	12	124952436	124952436	Human	1	name
405212901	CV2974307	single nucleotide variant	NM_032656.4(DHX37):c.1987G>A (p.Ala663Thr)	not provided [RCV003679478]	uncertain significance	12	124964452	124964452	Human		name
402490863	CV3011854	single nucleotide variant	NM_032656.4(DHX37):c.2590G>T (p.Ala864Ser)	not provided [RCV003687519]	uncertain significance	12	124953985	124953985	Human		name
402506791	CV3039203	single nucleotide variant	NM_032656.4(DHX37):c.1094G>A (p.Arg365Gln)	not provided [RCV003715278]	uncertain significance	12	124971399	124971399	Human		name
402509334	CV3042386	single nucleotide variant	NM_032656.4(DHX37):c.2148C>A (p.Asn716Lys)	not provided [RCV003715541]	uncertain significance	12	124960321	124960321	Human		name
405132986	CV3051361	single nucleotide variant	NM_032656.4(DHX37):c.2032G>A (p.Gly678Ser)	not provided [RCV003724995]	uncertain significance	12	124964407	124964407	Human		name
405206703	CV3064398	single nucleotide variant	NM_032656.4(DHX37):c.2795G>C (p.Gly932Ala)	not provided [RCV003731402]	uncertain significance	12	124952471	124952471	Human		name
405230625	CV3073311	single nucleotide variant	NM_032656.4(DHX37):c.2470G>A (p.Glu824Lys)	Inborn genetic diseases [RCV004374282]\|not provided [RCV003734833]	uncertain significance	12	124954195	124954195	Human	1	name
405699513	CV3227199	single nucleotide variant	NM_032656.4(DHX37):c.1829C>T (p.Pro610Leu)	46,XY sex reversal 11 [RCV003993550]	uncertain significance	12	124964610	124964610	Human	2	name
405692808	CV3243714	single nucleotide variant	NM_032656.4(DHX37):c.1731T>G (p.Asp577Glu)	Inborn genetic diseases [RCV004373605]	uncertain significance	12	124965672	124965672	Human	1	name
405692812	CV3243715	single nucleotide variant	NM_032656.4(DHX37):c.2166C>A (p.Asn722Lys)	Inborn genetic diseases [RCV004373606]	uncertain significance	12	124957127	124957127	Human	1	name
405692822	CV3243717	single nucleotide variant	NM_032656.4(DHX37):c.2653A>G (p.Met885Val)	Inborn genetic diseases [RCV004373608]\|not provided [RCV005103384]	uncertain significance	12	124953922	124953922	Human	1	name
405692826	CV3243718	single nucleotide variant	NM_032656.4(DHX37):c.2747C>T (p.Pro916Leu)	Inborn genetic diseases [RCV004373609]	uncertain significance	12	124952519	124952519	Human	1	name
405692834	CV3243719	single nucleotide variant	NM_032656.4(DHX37):c.2884G>A (p.Asp962Asn)	Inborn genetic diseases [RCV004373610]	uncertain significance	12	124950789	124950789	Human	1	name
405692838	CV3243720	single nucleotide variant	NM_032656.4(DHX37):c.2929C>T (p.Pro977Ser)	Inborn genetic diseases [RCV004373611]	uncertain significance	12	124950744	124950744	Human	1	name
407467485	CV3434165	single nucleotide variant	NM_032656.4(DHX37):c.2543C>T (p.Ala848Val)	Inborn genetic diseases [RCV004614226]	uncertain significance	12	124954122	124954122	Human	1	name
408393862	CV3519963	single nucleotide variant	NM_032656.4(DHX37):c.1739A>G (p.Glu580Gly)	not provided [RCV004764259]	uncertain significance	12	124965003	124965003	Human		name
408386232	CV3522429	single nucleotide variant	NM_032656.4(DHX37):c.2570T>C (p.Val857Ala)	Inborn genetic diseases [RCV005325925]\|not provided [RCV004767789]	uncertain significance	12	124954095	124954095	Human	1	name
408389743	CV3524706	single nucleotide variant	NM_032656.4(DHX37):c.2212G>T (p.Glu738Ter)	not provided [RCV004769601]	uncertain significance	12	124957081	124957081	Human		name
596924218	CV3532137	single nucleotide variant	NM_032656.4(DHX37):c.1235G>A (p.Arg412Gln)	not provided [RCV004777248]	uncertain significance	12	124968925	124968925	Human		name
596924311	CV3532209	single nucleotide variant	NM_032656.4(DHX37):c.2263A>G (p.Arg755Gly)	not provided [RCV004777320]	uncertain significance	12	124957030	124957030	Human		name
596924585	CV3535736	single nucleotide variant	NM_032656.4(DHX37):c.1000C>T (p.Arg334Trp)	46,XY sex reversal 11 [RCV004787184]	conflicting interpretations of pathogenicity	12	124972580	124972580	Human	2	name
597658064	CV3652401	single nucleotide variant	NM_032656.4(DHX37):c.2704G>A (p.Val902Met)	Inborn genetic diseases [RCV004976839]	uncertain significance	12	124952562	124952562	Human	1	name
597658077	CV3652403	single nucleotide variant	NM_032656.4(DHX37):c.2309C>T (p.Ala770Val)	Inborn genetic diseases [RCV004976841]	uncertain significance	12	124956835	124956835	Human	1	name
597658091	CV3652407	single nucleotide variant	NM_032656.4(DHX37):c.2182C>T (p.Pro728Ser)	Inborn genetic diseases [RCV004976844]	uncertain significance	12	124957111	124957111	Human	1	name
597658109	CV3652410	single nucleotide variant	NM_032656.4(DHX37):c.1342C>A (p.Pro448Thr)	Inborn genetic diseases [RCV004976847]	uncertain significance	12	124968600	124968600	Human	1	name
597658114	CV3652411	single nucleotide variant	NM_032656.4(DHX37):c.2633A>G (p.Asn878Ser)	Inborn genetic diseases [RCV004976848]	uncertain significance	12	124953942	124953942	Human	1	name
597658134	CV3652416	single nucleotide variant	NM_032656.4(DHX37):c.2588G>A (p.Gly863Glu)	Inborn genetic diseases [RCV004976852]\|not provided [RCV005110178]	uncertain significance	12	124953987	124953987	Human	1	name
597658144	CV3652418	single nucleotide variant	NM_032656.4(DHX37):c.2506G>T (p.Val836Leu)	Inborn genetic diseases [RCV004976854]	uncertain significance	12	124954159	124954159	Human	1	name
597658157	CV3652421	single nucleotide variant	NM_032656.4(DHX37):c.2186C>A (p.Pro729His)	Inborn genetic diseases [RCV004976857]	uncertain significance	12	124957107	124957107	Human	1	name
597907450	CV3773215	single nucleotide variant	NM_032656.4(DHX37):c.2894T>C (p.Phe965Ser)	not provided [RCV005113280]	uncertain significance	12	124950779	124950779	Human		name
597884613	CV3799635	single nucleotide variant	NM_032656.4(DHX37):c.2024C>T (p.Thr675Met)	not provided [RCV005150302]	likely benign	12	124964415	124964415	Human		name
597971829	CV3833189	single nucleotide variant	NM_032656.4(DHX37):c.1015G>A (p.Val339Met)	not provided [RCV005167086]	uncertain significance	12	124972565	124972565	Human		name
597867534	CV3838718	single nucleotide variant	NM_032656.4(DHX37):c.2177C>T (p.Pro726Leu)	not provided [RCV005176014]	uncertain significance	12	124957116	124957116	Human		name
597946577	CV3841685	single nucleotide variant	NM_032656.4(DHX37):c.1393C>T (p.Arg465Trp)	Inborn genetic diseases [RCV005326051]\|not provided [RCV005189119]	uncertain significance	12	124968549	124968549	Human	1	name
597916847	CV3841988	single nucleotide variant	NM_032656.4(DHX37):c.1630C>T (p.Pro544Ser)	not provided [RCV005183662]	uncertain significance	12	124965773	124965773	Human		name
597954369	CV3844403	single nucleotide variant	NM_032656.4(DHX37):c.1495C>T (p.Arg499Trp)	not provided [RCV005191076]	uncertain significance	12	124967132	124967132	Human		name
597872042	CV3849427	single nucleotide variant	NM_032656.4(DHX37):c.2171C>T (p.Pro724Leu)	not provided [RCV005197608]	uncertain significance	12	124957122	124957122	Human		name
597948477	CV3852506	single nucleotide variant	NM_032656.4(DHX37):c.1091T>C (p.Leu364Pro)	not provided [RCV005189584]	uncertain significance	12	124971402	124971402	Human		name
597905116	CV3853074	single nucleotide variant	NM_032656.4(DHX37):c.1280C>T (p.Pro427Leu)	not provided [RCV005202731]	uncertain significance	12	124968880	124968880	Human		name
597887814	CV3859388	single nucleotide variant	NM_032656.4(DHX37):c.1792G>A (p.Ala598Thr)	not provided [RCV005200044]	uncertain significance	12	124964950	124964950	Human		name
598127114	CV3888023	single nucleotide variant	NM_032656.4(DHX37):c.2979G>A (p.Met993Ile)	not provided [RCV005242709]	uncertain significance	12	124950694	124950694	Human		name
12859002	CV389152	single nucleotide variant	NM_032656.4(DHX37):c.1460G>A (p.Arg487His)	46,XY sex reversal 11 [RCV003227484]\|Abnormal brain morphology [RCV000454335]\|Neurodevelopmental disorder with brain anomalies and with or without vertebral or cardiac anomalies [RCV003333070]\|not provided [RCV004719818]	likely pathogenic\|uncertain significance	12	124967167	124967167	Human	4	name
12858905	CV389153	single nucleotide variant	NM_032656.4(DHX37):c.1257C>A (p.Asn419Lys)	Abnormal brain morphology [RCV000454218]\|Intellectual disability [RCV000853095]\|Neurodevelopmental disorder with brain anomalies and with or without vertebral or cardiac anomalies [RCV000991233]\|Neurodevelopmental disorders [RCV001261667]	pathogenic\|likely pathogenic	12	124968903	124968903	Human	6	name
598218713	CV3895546	single nucleotide variant	NM_032656.4(DHX37):c.2776C>T (p.Arg926Ter)	46,XY sex reversal 11 [RCV005360401]	uncertain significance	12	124952490	124952490	Human	2	name
598171500	CV3953183	single nucleotide variant	NM_032656.4(DHX37):c.1874C>T (p.Thr625Met)	Inborn genetic diseases [RCV005331192]	uncertain significance	12	124964565	124964565	Human	1	name
598171506	CV3953184	single nucleotide variant	NM_032656.4(DHX37):c.1322T>C (p.Val441Ala)	Inborn genetic diseases [RCV005331193]	uncertain significance	12	124968620	124968620	Human	1	name
598171510	CV3953185	single nucleotide variant	NM_032656.4(DHX37):c.2428C>T (p.Arg810Trp)	Inborn genetic diseases [RCV005331194]	uncertain significance	12	124956716	124956716	Human	1	name
617150779	CV4019228	single nucleotide variant	NM_032656.4(DHX37):c.2622T>G (p.Phe874Leu)	not provided [RCV005423636]	uncertain significance	12	124953953	124953953	Human		name
14702453	CV626213	single nucleotide variant	NM_032656.4(DHX37):c.2453G>A (p.Arg818Lys)	not specified [RCV000790929]	uncertain significance	12	124956691	124956691	Human		name
15015035	CV679682	single nucleotide variant	NM_032656.4(DHX37):c.2191G>A (p.Val731Met)	Neurodevelopmental disorder with brain anomalies and with or without vertebral or cardiac anomalies [RCV000991235]\|Neurodevelopmental disorders [RCV001261669]\|Seizure [RCV000853097]	pathogenic\|likely pathogenic	12	124957102	124957102	Human	6	name
15015034	CV679683	single nucleotide variant	NM_032656.4(DHX37):c.1399C>G (p.Leu467Val)	Neurodevelopmental disorders [RCV001261668]\|Seizure [RCV000853096]\|not provided [RCV001532726]	likely pathogenic\|uncertain significance	12	124968543	124968543	Human	5	name
15015038	CV679684	single nucleotide variant	NM_032656.4(DHX37):c.1145A>G (p.Asp382Gly)	Coloboma of optic nerve [RCV000853100]\|Neurodevelopmental disorders [RCV001261672]	likely pathogenic	12	124971348	124971348	Human	11	name
15135234	CV713430	single nucleotide variant	NM_032656.4(DHX37):c.1524A>C (p.Lys508Asn)	DHX37-related disorder [RCV003943142]\|not provided [RCV000965254]	benign	12	124966859	124966859	Human	1	name , trait , alternate_id
8627216	CV82360	single nucleotide variant	NM_032656.3(DHX37):c.1754C>T (p.Ser585Phe)	Malignant melanoma [RCV000062439]	not provided	12	124964988	124964988	Human		name
26902603	CV857636	single nucleotide variant	NM_032656.4(DHX37):c.2020C>T (p.Arg674Trp)	46,XY sex reversal 11 [RCV001089511]\|DHX37-related disorder [RCV003396737]	pathogenic\|likely pathogenic	12	124964419	124964419	Human	3	name , trait , alternate_id
26902604	CV857637	single nucleotide variant	NM_032656.4(DHX37):c.1784C>T (p.Ser595Phe)	46,XY sex reversal 11 [RCV001089512]	pathogenic	12	124964958	124964958	Human	2	name
26902606	CV857638	single nucleotide variant	NM_032656.4(DHX37):c.2021G>A (p.Arg674Gln)	46,XY sex reversal 11 [RCV001089513]\|not provided [RCV004720759]	pathogenic\|likely pathogenic	12	124964418	124964418	Human	2	name
126725622	CV1017583	single nucleotide variant	NM_032656.4(DHX37):c.3302G>A (p.Arg1101His)	Inborn genetic diseases [RCV002546487]\|Neurodevelopmental disorder with brain anomalies and with or without vertebral or cardiac anomalies [RCV001331506]	uncertain significance	12	124948170	124948170	Human	2	name
150512380	CV1245415	single nucleotide variant	NM_032656.4(DHX37):c.3242G>A (p.Arg1081Gln)	46,XY sex reversal 11 [RCV001661398]\|Neurodevelopmental disorder with brain anomalies and with or without vertebral or cardiac anomalies [RCV001661397]\|not provided [RCV002539628]	benign	12	124950034	124950034	Human	3	name
152080124	CV1666904	single nucleotide variant	NM_032656.4(DHX37):c.3092G>A (p.Arg1031Gln)	DHX37-related disorder [RCV003933694]\|not provided [RCV002211249]	likely benign	12	124950442	124950442	Human	1	name , trait , alternate_id
152042795	CV1670046	single nucleotide variant	NM_032656.4(DHX37):c.3425C>G (p.Ala1142Gly)	Inborn genetic diseases [RCV003089192]\|not provided [RCV002224948]	uncertain significance	12	124947851	124947851	Human	1	name
152981689	CV1676995	single nucleotide variant	NM_032656.4(DHX37):c.3045C>G (p.Asp1015Glu)	not specified [RCV002248062]	benign	12	124950489	124950489	Human		name
153301896	CV1689357	single nucleotide variant	NM_032656.4(DHX37):c.3185A>C (p.Lys1062Thr)	not provided [RCV002267307]	uncertain significance	12	124950180	124950180	Human		name
156046937	CV1887537	single nucleotide variant	NM_032656.4(DHX37):c.3082G>A (p.Glu1028Lys)	Inborn genetic diseases [RCV003089658]\|not provided [RCV003078734]	conflicting interpretations of pathogenicity\|uncertain significance	12	124950452	124950452	Human	1	name
156404721	CV1898381	single nucleotide variant	NM_032656.4(DHX37):c.3436G>A (p.Asp1146Asn)	not provided [RCV002585474]	uncertain significance	12	124947840	124947840	Human		name
156062550	CV1931116	single nucleotide variant	NM_032656.4(DHX37):c.3125G>A (p.Arg1042His)	Inborn genetic diseases [RCV003162084]\|not provided [RCV002638335]	uncertain significance	12	124950240	124950240	Human	1	name
156129820	CV1966160	single nucleotide variant	NM_032656.4(DHX37):c.3268A>G (p.Thr1090Ala)	not provided [RCV002593451]	uncertain significance	12	124950008	124950008	Human		name
156349368	CV1968224	single nucleotide variant	NM_032656.4(DHX37):c.3089G>A (p.Gly1030Glu)	not provided [RCV002601711]	uncertain significance	12	124950445	124950445	Human		name
156038154	CV2030118	single nucleotide variant	NM_032656.4(DHX37):c.3196C>T (p.Arg1066Trp)	not provided [RCV002736079]	uncertain significance	12	124950169	124950169	Human		name
155987106	CV2030537	single nucleotide variant	NM_032656.4(DHX37):c.3178C>G (p.Arg1060Gly)	not provided [RCV002755587]	uncertain significance	12	124950187	124950187	Human		name
155971238	CV2030850	single nucleotide variant	NM_032656.4(DHX37):c.3143C>G (p.Pro1048Arg)	not provided [RCV002731633]	uncertain significance	12	124950222	124950222	Human		name
156190229	CV2037901	single nucleotide variant	NM_032656.4(DHX37):c.3313C>T (p.Leu1105Phe)	not provided [RCV002765886]	uncertain significance	12	124948159	124948159	Human		name
156034284	CV2079040	single nucleotide variant	NM_032656.4(DHX37):c.3302G>T (p.Arg1101Leu)	not provided [RCV002867181]	uncertain significance	12	124948170	124948170	Human		name
156100272	CV2099237	single nucleotide variant	NM_032656.4(DHX37):c.3179G>A (p.Arg1060His)	Inborn genetic diseases [RCV005333375]\|not provided [RCV002913376]	uncertain significance	12	124950186	124950186	Human	1	name
156040737	CV2121543	single nucleotide variant	NM_032656.4(DHX37):c.3322G>T (p.Ala1108Ser)	not provided [RCV002923906]	benign	12	124948150	124948150	Human		name
156184886	CV2152100	single nucleotide variant	NM_032656.4(DHX37):c.3046A>G (p.Lys1016Glu)	not provided [RCV003005823]	uncertain significance	12	124950488	124950488	Human		name
156210979	CV2170847	single nucleotide variant	NM_032656.4(DHX37):c.3223C>T (p.Arg1075Cys)	Inborn genetic diseases [RCV003367953]\|not provided [RCV003042330]	uncertain significance	12	124950053	124950053	Human	1	name
156231172	CV2199641	single nucleotide variant	NM_032656.4(DHX37):c.3407G>A (p.Cys1136Tyr)	Inborn genetic diseases [RCV002644960]	uncertain significance	12	124947869	124947869	Human	1	name
155915125	CV2243677	single nucleotide variant	NM_032656.4(DHX37):c.3178C>T (p.Arg1060Cys)	Inborn genetic diseases [RCV002772168]\|not provided [RCV003886603]	likely benign	12	124950187	124950187	Human	1	name
156349500	CV2305626	single nucleotide variant	NM_032656.4(DHX37):c.3265G>A (p.Gly1089Ser)	Inborn genetic diseases [RCV002939643]	likely benign	12	124950011	124950011	Human	1	name
156173968	CV2355221	single nucleotide variant	NM_032656.4(DHX37):c.3227A>C (p.Lys1076Thr)	Inborn genetic diseases [RCV002983642]	uncertain significance	12	124950049	124950049	Human	1	name
401779536	CV2676604	single nucleotide variant	NM_032656.4(DHX37):c.3151G>A (p.Glu1051Lys)	Inborn genetic diseases [RCV003264457]\|not provided [RCV004809986]	likely benign\|conflicting interpretations of pathogenicity\|uncertain significance	12	124950214	124950214	Human	1	name
401751428	CV2708617	single nucleotide variant	NM_032656.4(DHX37):c.3127G>C (p.Val1043Leu)	Inborn genetic diseases [RCV003277028]	uncertain significance	12	124950238	124950238	Human	1	name
401873083	CV2749715	single nucleotide variant	NM_032656.4(DHX37):c.3390C>A (p.Tyr1130Ter)	not provided [RCV003332844]	uncertain significance	12	124947886	124947886	Human		name
401854402	CV2777541	single nucleotide variant	NM_032656.4(DHX37):c.3086G>C (p.Arg1029Pro)	Inborn genetic diseases [RCV003338326]	uncertain significance	12	124950448	124950448	Human	1	name
405095014	CV2878417	single nucleotide variant	NM_032656.4(DHX37):c.3224G>A (p.Arg1075His)	not provided [RCV003550083]	likely benign	12	124950052	124950052	Human		name
405125008	CV2889482	single nucleotide variant	NM_032656.4(DHX37):c.3442G>A (p.Glu1148Lys)	not provided [RCV003559396]	likely benign	12	124947834	124947834	Human		name
402525089	CV2937102	single nucleotide variant	NM_032656.4(DHX37):c.3283T>C (p.Trp1095Arg)	not provided [RCV003663591]	uncertain significance	12	124949993	124949993	Human		name
405100535	CV2947917	single nucleotide variant	NM_032656.4(DHX37):c.3197G>A (p.Arg1066Gln)	not provided [RCV003665982]	uncertain significance	12	124950168	124950168	Human		name
405154544	CV3068779	single nucleotide variant	NM_032656.4(DHX37):c.3427A>G (p.Met1143Val)	not provided [RCV003726652]	uncertain significance	12	124947849	124947849	Human		name
405236151	CV3079491	single nucleotide variant	NM_032656.4(DHX37):c.3061C>A (p.Pro1021Thr)	not provided [RCV003735848]	uncertain significance	12	124950473	124950473	Human		name
405261195	CV3186100	single nucleotide variant	NM_032656.4(DHX37):c.3301C>T (p.Arg1101Cys)	Inborn genetic diseases [RCV004981130]\|not provided [RCV003885176]	uncertain significance	12	124948171	124948171	Human	1	name
405692843	CV3243721	single nucleotide variant	NM_032656.4(DHX37):c.3127G>A (p.Val1043Met)	Inborn genetic diseases [RCV004373612]	uncertain significance	12	124950238	124950238	Human	1	name
408376575	CV3514614	single nucleotide variant	NM_032656.4(DHX37):c.3050C>T (p.Pro1017Leu)	DHX37-related disorder [RCV004749251]	uncertain significance	12	124950484	124950484	Human		name , trait , alternate_id
597658082	CV3652405	single nucleotide variant	NM_032656.4(DHX37):c.3086G>A (p.Arg1029Gln)	Inborn genetic diseases [RCV004976842]	uncertain significance	12	124950448	124950448	Human	1	name
597658087	CV3652406	single nucleotide variant	NM_032656.4(DHX37):c.3311G>C (p.Ser1104Thr)	Inborn genetic diseases [RCV004976843]	uncertain significance	12	124948161	124948161	Human	1	name
597658103	CV3652409	single nucleotide variant	NM_032656.4(DHX37):c.3343G>A (p.Asp1115Asn)	Inborn genetic diseases [RCV004976846]	uncertain significance	12	124948129	124948129	Human	1	name
597658118	CV3652412	single nucleotide variant	NM_032656.4(DHX37):c.3107G>A (p.Arg1036Gln)	Inborn genetic diseases [RCV004976849]	uncertain significance	12	124950427	124950427	Human	1	name
597658137	CV3652417	single nucleotide variant	NM_032656.4(DHX37):c.3262C>G (p.Pro1088Ala)	Inborn genetic diseases [RCV004976853]	uncertain significance	12	124950014	124950014	Human	1	name
597658156	CV3652420	single nucleotide variant	NM_032656.4(DHX37):c.3037C>A (p.Gln1013Lys)	Inborn genetic diseases [RCV004976856]	uncertain significance	12	124950497	124950497	Human	1	name
597938174	CV3775036	single nucleotide variant	NM_032656.4(DHX37):c.3145G>A (p.Ala1049Thr)	not provided [RCV005117862]	uncertain significance	12	124950220	124950220	Human		name
598171512	CV3953186	single nucleotide variant	NM_032656.4(DHX37):c.3377A>G (p.Lys1126Arg)	Inborn genetic diseases [RCV005331195]	uncertain significance	12	124948095	124948095	Human	1	name
598171527	CV3953189	single nucleotide variant	NM_032656.4(DHX37):c.3367G>A (p.Ala1123Thr)	Inborn genetic diseases [RCV005331198]	uncertain significance	12	124948105	124948105	Human	1	name
15015039	CV679681	single nucleotide variant	NM_032656.4(DHX37):c.3281C>T (p.Thr1094Met)	Intellectual disability [RCV000853101]\|Neurodevelopmental disorders [RCV001261673]	likely pathogenic	12	124949995	124949995	Human	4	name
15135257	CV738537	single nucleotide variant	NM_032656.4(DHX37):c.3019C>G (p.Leu1007Val)	not provided [RCV000898425]	likely benign	12	124950515	124950515	Human		name
15194945	CV753197	single nucleotide variant	NM_032656.4(DHX37):c.3440T>C (p.Ile1147Thr)	DHX37-related disorder [RCV003913015]\|not provided [RCV000911270]	likely benign	12	124947836	124947836	Human	1	name , trait , alternate_id
152980466	CV1678625	deletion	NM_032656.4(DHX37):c.346_347del (p.Thr116fs)	not specified [RCV002247133]	uncertain significance	12	124982553	124982554	Human		name
156089026	CV1983935	deletion	NM_032656.4(DHX37):c.202_204del (p.Glu68del)	not provided [RCV002621795]	uncertain significance	12	124986168	124986170	Human		name
156323620	CV2173696	microsatellite	NM_032656.4(DHX37):c.478GAG[8] (p.Glu168del)	not provided [RCV003046783]	benign	12	124980724	124980726	Human		name
598124825	CV3883696	deletion	NM_032656.4(DHX37):c.226_228del (p.Glu76del)	not provided [RCV005236050]	uncertain significance	12	124986144	124986146	Human		name
15015037	CV679685	inversion	NM_032656.4(DHX37):c.499_500inv (p.Glu167Ser)	46,XY sex reversal 11 [RCV003334454]\|Intellectual disability [RCV000853099]\|Neurodevelopmental disorder with brain anomalies and with or without vertebral or cardiac anomalies [RCV000991237]\|Neurodevelopmental disorders [RCV001261671]	pathogenic\|likely pathogenic\|uncertain significance	12	124980728	124980729	Human		name
408388119	CV3520648	inversion	NM_032656.4(DHX37):c.2330_2331inv (p.Thr777Met)	not provided [RCV004761481]	uncertain significance	12	124956813	124956814	Human		name
156042453	CV2049791	indel	NM_032656.4(DHX37):c.288_289delinsAT (p.Met96Ile)	not provided [RCV002796486]	uncertain significance	12	124982611	124982612	Human		name
156158194	CV2033680	indel	NM_032656.4(DHX37):c.790_791delinsTT (p.Ala264Phe)	not provided [RCV002741449]	uncertain significance	12	124977438	124977439	Human		name
156205789	CV2092713	microsatellite	NM_032656.4(DHX37):c.478GAG[7] (p.Glu167_Glu168del)	not provided [RCV002917961]	uncertain significance	12	124980724	124980729	Human		name
402483894	CV2998179	indel	NM_032656.4(DHX37):c.2498_2499delinsTC (p.Arg833Leu)	not provided [RCV003686877]	uncertain significance	12	124954166	124954167	Human		name
156232380	CV2075063	microsatellite	NM_032656.4(DHX37):c.478GAG[10] (p.Glu168_Ser169insGlu)	DHX37-related disorder [RCV003936324]\|not provided [RCV002830099]	benign\|likely benign	12	124980723	124980724	Human		name , trait , alternate_id
155946377	CV2107874	microsatellite	NM_032656.4(DHX37):c.478GAG[11] (p.Glu168_Ser169insGluGlu)	DHX37-related disorder [RCV003963426]\|not provided [RCV002904789]	benign\|uncertain significance	12	124980723	124980724	Human		name , trait , alternate_id
596926254	CV3536180	duplication	NM_032656.4(DHX37):c.510_515dup (p.Glu172_Leu173insSerGlu)	Neurodevelopmental disorder with brain anomalies and with or without vertebral or cardiac anomalies [RCV004788610]	uncertain significance	12	124980712	124980713	Human	1	name
156200190	CV1916719	microsatellite	NM_032656.4(DHX37):c.478GAG[12] (p.Glu168_Ser169insGluGluGlu)	not provided [RCV002595675]	uncertain significance	12	124980723	124980724	Human		name
156406306	CV1921533	microsatellite	NM_032656.4(DHX37):c.478GAG[13] (p.Glu168_Ser169insGluGluGluGlu)	not provided [RCV002606551]	uncertain significance	12	124980723	124980724	Human		name

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