dbVar data for all organisms

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Variant Placements for nstd166 (displaying 100 of 304733 variants)
Study ID	Variant ID	Variant Region type	Validation	Assembly	Accession	Chr	Start	End	Placement Type	Remap Score
nstd166	nsv4032485	copy number variation	No	GRCh38.p12	NC_000001.11	1	938039	938669	Remapped	1
nstd166	nsv4032969	copy number variation	No	GRCh38.p12	NC_000001.11	1	978571	1048804	Remapped	1
nstd166	nsv4032982	copy number variation	No	GRCh38.p12	NC_000001.11	1	963745	963820	Remapped	1
nstd166	nsv4033012	copy number variation	No	GRCh38.p12	NC_000001.11	1	257999	289549	Remapped	1
nstd166	nsv4033399	copy number variation	No	GRCh38.p12	NC_000001.11	1	750620	765045	Remapped	1
nstd166	nsv4033712	copy number variation	No	GRCh38.p12	NC_000001.11	1	952174	954014	Remapped	1
nstd166	nsv4033807	copy number variation	No	GRCh38.p12	NC_000001.11	1	792712	841500	Remapped	1
nstd166	nsv4033895	copy number variation	No	GRCh38.p12	NC_000001.11	1	886284	902447	Remapped	1
nstd166	nsv4034043	copy number variation	No	GRCh38.p12	NC_000001.11	1	948661	948730	Remapped	1
nstd166	nsv4034076	copy number variation	No	GRCh38.p12	NC_000001.11	1	1000469	1034068	Remapped	1
nstd166	nsv4034405	copy number variation	No	GRCh38.p12	NC_000001.11	1	872969	873107	Remapped	1
nstd166	nsv4034505	copy number variation	No	GRCh38.p12	NC_000001.11	1	821192	823223	Remapped	1
nstd166	nsv4034659	copy number variation	No	GRCh38.p12	NC_000001.11	1	94000	129400	Remapped	1
nstd166	nsv4034991	copy number variation	No	GRCh38.p12	NC_000001.11	1	904469	904570	Remapped	1
nstd166	nsv4035122	copy number variation	No	GRCh38.p12	NC_000001.11	1	1016948	1017061	Remapped	1
nstd166	nsv4035416	copy number variation	No	GRCh38.p12	NC_000001.11	1	639370	646570	Remapped	1
nstd166	nsv4035427	copy number variation	No	GRCh38.p12	NC_000001.11	1	841389	856501	Remapped	1
nstd166	nsv4035690	copy number variation	No	GRCh38.p12	NC_000001.11	1	823179	823473	Remapped	1
nstd166	nsv4036682	copy number variation	No	GRCh38.p12	NC_000001.11	1	940874	944653	Remapped	1
nstd166	nsv4036772	copy number variation	No	GRCh38.p12	NC_000001.11	1	62399	62489	Remapped	1
nstd166	nsv4036810	copy number variation	No	GRCh38.p12	NC_000001.11	1	977732	977942	Remapped	1
nstd166	nsv4037415	copy number variation	No	GRCh38.p12	NC_000001.11	1	818880	922261	Remapped	1
nstd166	nsv4038463	copy number variation	No	GRCh38.p12	NC_000001.11	1	981576	981643	Remapped	1
nstd166	nsv4038489	copy number variation	No	GRCh38.p12	NC_000001.11	1	831216	833732	Remapped	1
nstd166	nsv4038561	copy number variation	No	GRCh38.p12	NC_000001.11	1	976420	982620	Remapped	1
nstd166	nsv4038743	copy number variation	No	GRCh38.p12	NC_000001.11	1	722620	740620	Remapped	1
nstd166	nsv4039163	copy number variation	No	GRCh38.p12	NC_000001.11	1	979844	979980	Remapped	1
nstd166	nsv4039615	copy number variation	No	GRCh38.p12	NC_000001.11	1	586420	611470	Remapped	1
nstd166	nsv4039740	copy number variation	No	GRCh38.p12	NC_000001.11	1	123350	140100	Remapped	1
nstd166	nsv4039815	copy number variation	No	GRCh38.p12	NC_000001.11	1	809320	815620	Remapped	1
nstd166	nsv4039931	copy number variation	No	GRCh38.p12	NC_000001.11	1	937391	938843	Remapped	1
nstd166	nsv4040204	copy number variation	No	GRCh38.p12	NC_000001.11	1	839207	893055	Remapped	1
nstd166	nsv4040207	copy number variation	No	GRCh38.p12	NC_000001.11	1	950424	950509	Remapped	1
nstd166	nsv4040585	copy number variation	No	GRCh38.p12	NC_000001.11	1	820060	821136	Remapped	1
nstd166	nsv4040862	copy number variation	No	GRCh38.p12	NC_000001.11	1	936277	936389	Remapped	1
nstd166	nsv4041087	copy number variation	No	GRCh38.p12	NC_000001.11	1	822735	822992	Remapped	1
nstd166	nsv4041434	copy number variation	No	GRCh38.p12	NC_000001.11	1	968320	970242	Remapped	1
nstd166	nsv4042148	copy number variation	No	GRCh38.p12	NC_000001.11	1	906939	907008	Remapped	1
nstd166	nsv4042173	copy number variation	No	GRCh38.p12	NC_000001.11	1	663920	669870	Remapped	1
nstd166	nsv4043338	copy number variation	No	GRCh38.p12	NC_000001.11	1	667950	668023	Remapped	1
nstd166	nsv4043403	copy number variation	No	GRCh38.p12	NC_000001.11	1	1029120	1042620	Remapped	1
nstd166	nsv4043441	copy number variation	No	GRCh38.p12	NC_000001.11	1	1011741	1012525	Remapped	1
nstd166	nsv4044232	copy number variation	No	GRCh38.p12	NC_000001.11	1	909520	914620	Remapped	1
nstd166	nsv4044683	copy number variation	No	GRCh38.p12	NC_000001.11	1	274165	274481	Remapped	1
nstd166	nsv4045041	copy number variation	No	GRCh38.p12	NC_000001.11	1	636370	649645	Remapped	1
nstd166	nsv4045042	copy number variation	No	GRCh38.p12	NC_000001.11	1	822041	898948	Remapped	1
nstd166	nsv4045056	copy number variation	No	GRCh38.p12	NC_000001.11	1	811384	811951	Remapped	1
nstd166	nsv4045105	copy number variation	No	GRCh38.p12	NC_000001.11	1	137000	155500	Remapped	1
nstd166	nsv4045512	copy number variation	No	GRCh38.p12	NC_000001.11	1	960370	967120	Remapped	1
nstd166	nsv4046119	copy number variation	No	GRCh38.p12	NC_000001.11	1	859112	864158	Remapped	1
nstd166	nsv4046332	copy number variation	No	GRCh38.p12	NC_000001.11	1	733250	914825	Remapped	1
nstd166	nsv4046486	copy number variation	No	GRCh38.p12	NC_000001.11	1	986620	991620	Remapped	1
nstd166	nsv4046689	copy number variation	No	GRCh38.p12	NC_000001.11	1	803230	806636	Remapped	1
nstd166	nsv4047355	copy number variation	No	GRCh38.p12	NC_000001.11	1	833560	908076	Remapped	1
nstd166	nsv4047701	copy number variation	No	GRCh38.p12	NC_000001.11	1	612219	612422	Remapped	1
nstd166	nsv4048266	copy number variation	No	GRCh38.p12	NC_000001.11	1	910141	912111	Remapped	1
nstd166	nsv4048468	copy number variation	No	GRCh38.p12	NC_000001.11	1	667620	687620	Remapped	1
nstd166	nsv4048580	copy number variation	No	GRCh38.p12	NC_000001.11	1	933899	934725	Remapped	1
nstd166	nsv4048595	copy number variation	No	GRCh38.p12	NC_000001.11	1	888541	888617	Remapped	1
nstd166	nsv4048721	copy number variation	No	GRCh38.p12	NC_000001.11	1	141475	155000	Remapped	1
nstd166	nsv4049200	copy number variation	No	GRCh38.p12	NC_000001.11	1	491687	499337	Remapped	1
nstd166	nsv4050524	copy number variation	No	GRCh38.p12	NC_000001.11	1	859016	929737	Remapped	1
nstd166	nsv4050917	copy number variation	No	GRCh38.p12	NC_000001.11	1	417587	455337	Remapped	1
nstd166	nsv4051037	copy number variation	No	GRCh38.p12	NC_000001.11	1	1011045	1012334	Remapped	1
nstd166	nsv4051827	copy number variation	No	GRCh38.p12	NC_000001.11	1	460337	465337	Remapped	1
nstd166	nsv4052006	copy number variation	No	GRCh38.p12	NC_000001.11	1	965775	968792	Remapped	1
nstd166	nsv4052009	copy number variation	No	GRCh38.p12	NC_000001.11	1	617920	629020	Remapped	1
nstd166	nsv4052037	copy number variation	No	GRCh38.p12	NC_000001.11	1	66350	66427	Remapped	1
nstd166	nsv4279519	insertion	No	GRCh38.p12	NC_000001.11	1	893801	893801	Remapped	1
nstd166	nsv4290545	insertion	No	GRCh38.p12	NC_000001.11	1	595506	595506	Remapped	1
nstd166	nsv4320551	sequence alteration	No	GRCh38.p12	NC_000001.11	1	839189	893055	Remapped	1
nstd166	nsv4462122	mobile element insertion	No	GRCh38.p12	NC_000001.11	1	883427	883427	Remapped	1
nstd166	nsv4462446	mobile element insertion	No	GRCh38.p12	NC_000001.11	1	913935	913935	Remapped	1
nstd166	nsv4501996	copy number variation	No	GRCh38.p12	NC_000001.11	1	431337	436337	Remapped	1
nstd166	nsv4509904	copy number variation	No	GRCh38.p12	NC_000001.11	1	624870	635220	Remapped	1
nstd166	nsv4514092	copy number variation	No	GRCh38.p12	NC_000001.11	1	46000	111250	Remapped	1
nstd166	nsv4516656	copy number variation	No	GRCh38.p12	NC_000001.11	1	883120	888620	Remapped	1
nstd166	nsv4516696	copy number variation	No	GRCh38.p12	NC_000001.11	1	1028476	1029081	Remapped	1
nstd166	nsv4516744	copy number variation	No	GRCh38.p12	NC_000001.11	1	964411	964820	Remapped	1
nstd166	nsv4517448	copy number variation	No	GRCh38.p12	NC_000001.11	1	906939	907032	Remapped	1
nstd166	nsv4517655	copy number variation	No	GRCh38.p12	NC_000001.11	1	595720	678370	Remapped	1
nstd166	nsv4517661	copy number variation	No	GRCh38.p12	NC_000001.11	1	732345	788620	Remapped	1
nstd166	nsv4517850	copy number variation	No	GRCh38.p12	NC_000001.11	1	820327	820512	Remapped	1
nstd166	nsv4517890	copy number variation	No	GRCh38.p12	NC_000001.11	1	792620	798270	Remapped	1
nstd166	nsv4518347	copy number variation	No	GRCh38.p12	NC_000001.11	1	868620	876620	Remapped	1
nstd166	nsv4533503	insertion	No	GRCh38.p12	NC_000001.11	1	776293	776293	Remapped	1
nstd166	nsv4533532	insertion	No	GRCh38.p12	NC_000001.11	1	79210	79210	Remapped	1
nstd166	nsv4533748	insertion	No	GRCh38.p12	NC_000001.11	1	984618	984618	Remapped	1
nstd166	nsv4534208	insertion	No	GRCh38.p12	NC_000001.11	1	66531	66531	Remapped	1
nstd166	nsv4534368	insertion	No	GRCh38.p12	NC_000001.11	1	904636	904636	Remapped	1
nstd166	nsv4534482	insertion	No	GRCh38.p12	NC_000001.11	1	904526	904526	Remapped	1
nstd166	nsv4534800	insertion	No	GRCh38.p12	NC_000001.11	1	66576	66576	Remapped	1
nstd166	nsv4536437	insertion	No	GRCh38.p12	NC_000001.11	1	54665	54665	Remapped	1
nstd166	nsv4536905	insertion	No	GRCh38.p12	NC_000001.11	1	823371	823371	Remapped	1
nstd166	nsv4537392	insertion	No	GRCh38.p12	NC_000001.11	1	823381	823381	Remapped	1
nstd166	nsv4537581	insertion	No	GRCh38.p12	NC_000001.11	1	904628	904628	Remapped	1
nstd166	nsv4537682	insertion	No	GRCh38.p12	NC_000001.11	1	978830	978830	Remapped	1
nstd166	nsv4558894	mobile element insertion	No	GRCh38.p12	NC_000001.11	1	784940	784940	Remapped	1
nstd166	nsv4560757	mobile element insertion	No	GRCh38.p12	NC_000001.11	1	887878	887878	Remapped	1
nstd166	nsv4568713	mobile element insertion	No	GRCh38.p12	NC_000001.11	1	983238	983238	Remapped	1

dbVar

Database of genomic structural variation

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