dbVar data for all organisms

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Variant Placements for nstd12 (displaying 100 of 2290 variants)
Study ID	Variant ID	Variant Region type	Validation	Assembly	Accession	Chr	Inner-Start	Inner-End	Placement Type	Remap Score
nstd12	nsv429712	copy number variation	No	GRCh38.p12	NC_000001.11	1	817186	1881249	Remapped	1.01106
nstd12	nsv429713	copy number variation	No	GRCh38.p12	NC_000001.11	1	16501296	16719151	Remapped	1
nstd12	nsv429714	copy number variation	No	GRCh38.p12	NC_000001.11	1	161541155	161669769	Remapped	2.72334
nstd12	nsv429725	copy number variation	No	GRCh38.p12	NC_000001.11	1	161544512	161703892	Remapped	2.04377
nstd12	nsv429758	copy number variation	No	GRCh38.p12	NC_000001.11	1	161544512	161669769	Remapped	2.85521
nstd12	nsv429824	copy number variation	No	GRCh38.p12	NC_000001.11	1	16501296	16617349	Remapped	1
nstd12	nsv429825	copy number variation	No	GRCh38.p12	NC_000001.11	1	161544512	161706767	Remapped	2.00665
nstd12	nsv429891	copy number variation	No	GRCh38.p12	NC_000001.11	1	163664613	163999105	Remapped	1.00147
nstd12	nsv429902	copy number variation	No	GRCh38.p12	NC_000001.11	1	165562105	165605105	Remapped	1
nstd12	nsv429913	copy number variation	No	GRCh38.p12	NC_000001.11	1	169207781	169327506	Remapped	1
nstd12	nsv429924	copy number variation	No	GRCh38.p12	NC_000001.11	1	175141344	175165178	Remapped	1
nstd12	nsv429935	copy number variation	No	GRCh38.p12	NC_000001.11	1	16568781	16642600	Remapped	1
nstd12	nsv429936	copy number variation	No	GRCh38.p12	NC_000001.11	1	179821208	180245208	Remapped	1
nstd12	nsv430046	copy number variation	No	GRCh38.p12	NC_000001.11	1	16568781	16719199	Remapped	1
nstd12	nsv430157	copy number variation	No	GRCh38.p12	NC_000001.11	1	16568781	16719151	Remapped	1
nstd12	nsv430268	copy number variation	No	GRCh38.p12	NC_000001.11	1	16597840	16719151	Remapped	1
nstd12	nsv430379	copy number variation	No	GRCh38.p12	NC_000001.11	1	16919676	17226380	Remapped	1
nstd12	nsv430490	copy number variation	No	GRCh38.p12	NC_000001.11	1	23178301	23386001	Remapped	1
nstd12	nsv430601	copy number variation	No	GRCh38.p12	NC_000001.11	1	26174567	26413467	Remapped	1
nstd12	nsv430712	copy number variation	No	GRCh38.p12	NC_000001.11	1	26220867	26413467	Remapped	1
nstd12	nsv430823	copy number variation	No	GRCh38.p12	NC_000001.11	1	1881249	2351874	Remapped	1
nstd12	nsv430824	copy number variation	No	GRCh38.p12	NC_000001.11	1	26538567	26851367	Remapped	1
nstd12	nsv430935	copy number variation	No	GRCh38.p12	NC_000001.11	1	32695277	32773113	Remapped	1
nstd12	nsv431046	copy number variation	No	GRCh38.p12	NC_000001.11	1	37156469	37221817	Remapped	1
nstd12	nsv431157	copy number variation	No	GRCh38.p12	NC_000001.11	1	41328846	41789550	Remapped	1
nstd12	nsv431268	copy number variation	No	GRCh38.p12	NC_000001.11	1	45757408	46029808	Remapped	1
nstd12	nsv431379	copy number variation	No	GRCh38.p12	NC_000001.11	1	57758540	58336936	Remapped	1
nstd12	nsv431490	copy number variation	No	GRCh38.p12	NC_000001.11	1	59242607	59327307	Remapped	1
nstd12	nsv431601	copy number variation	No	GRCh38.p12	NC_000001.11	1	60191507	61248607	Remapped	1
nstd12	nsv431712	copy number variation	No	GRCh38.p12	NC_000001.11	1	62293697	62300329	Remapped	1
nstd12	nsv431823	copy number variation	No	GRCh38.p12	NC_000001.11	1	65471382	65535719	Remapped	1
nstd12	nsv431934	copy number variation	No	GRCh38.p12	NC_000001.11	1	2348979	2487186	Remapped	1
nstd12	nsv431935	copy number variation	No	GRCh38.p12	NC_000001.11	1	66248901	66330565	Remapped	1
nstd12	nsv432046	copy number variation	No	GRCh38.p12	NC_000001.11	1	72546496	72622496	Remapped	1
nstd12	nsv432157	copy number variation	No	GRCh38.p12	NC_000001.11	1	72546496	72622475	Remapped	1
nstd12	nsv432268	copy number variation	No	GRCh38.p12	NC_000001.11	1	72546545	72622475	Remapped	1
nstd12	nsv432376	copy number variation	No	GRCh38.p12	NC_000001.11	1	73292434	73350881	Remapped	1
nstd12	nsv432387	copy number variation	No	GRCh38.p12	NC_000001.11	1	74529541	74542727	Remapped	1
nstd12	nsv432398	copy number variation	No	GRCh38.p12	NC_000001.11	1	77241706	77275151	Remapped	1
nstd12	nsv432409	copy number variation	No	GRCh38.p12	NC_000001.11	1	79896294	79937494	Remapped	1
nstd12	nsv432420	copy number variation	No	GRCh38.p12	NC_000001.11	1	80913084	80976865	Remapped	1
nstd12	nsv432431	copy number variation	No	GRCh38.p12	NC_000001.11	1	87219432	87275951	Remapped	1
nstd12	nsv432442	copy number variation	No	GRCh38.p12	NC_000001.11	1	2499178	2927689	Remapped	1.05901
nstd12	nsv432443	copy number variation	No	GRCh38.p12	NC_000001.11	1	87233875	87253392	Remapped	1
nstd12	nsv432454	copy number variation	No	GRCh38.p12	NC_000001.11	1	87233875	87246573	Remapped	1
nstd12	nsv432465	copy number variation	No	GRCh38.p12	NC_000001.11	1	87239647	87263640	Remapped	1
nstd12	nsv432476	copy number variation	No	GRCh38.p12	NC_000001.11	1	89772459	89874110	Remapped	1
nstd12	nsv432487	copy number variation	No	GRCh38.p12	NC_000001.11	1	90359094	90466208	Remapped	1.00001
nstd12	nsv432498	copy number variation	No	GRCh38.p12	NC_000001.11	1	91752688	92152766	Remapped	1
nstd12	nsv432509	copy number variation	No	GRCh38.p12	NC_000001.11	1	94654234	94686257	Remapped	1
nstd12	nsv432520	copy number variation	No	GRCh38.p12	NC_000001.11	1	97094023	98186523	Remapped	1
nstd12	nsv432531	copy number variation	No	GRCh38.p12	NC_000001.11	1	98059423	98138623	Remapped	1
nstd12	nsv432542	copy number variation	No	GRCh38.p12	NC_000001.11	1	101447971	101534513	Remapped	1
nstd12	nsv432553	copy number variation	No	GRCh38.p12	NC_000001.11	1	4922326	4938325	Remapped	1
nstd12	nsv432554	copy number variation	No	GRCh38.p12	NC_000001.11	1	103207881	103586151	Remapped	0.83075
nstd12	nsv432565	copy number variation	No	GRCh38.p12	NC_000001.11	1	103497357	103614357	Remapped	1
nstd12	nsv432576	copy number variation	No	GRCh38.p12	NC_000001.11	1	105458950	105544358	Remapped	1
nstd12	nsv432587	copy number variation	No	GRCh38.p12	NC_000001.11	1	105602040	106134751	Remapped	0.99996
nstd12	nsv432598	copy number variation	No	GRCh38.p12	NC_000001.11	1	107791336	107991619	Remapped	1
nstd12	nsv432609	copy number variation	No	GRCh38.p12	NC_000001.11	1	108311336	108346655	Remapped	1
nstd12	nsv432620	copy number variation	No	GRCh38.p12	NC_000001.11	1	112167693	112182315	Remapped	1
nstd12	nsv432631	copy number variation	No	GRCh38.p12	NC_000001.11	1	112529212	112658175	Remapped	1
nstd12	nsv432642	copy number variation	No	GRCh38.p12	NC_000001.11	1	116449336	116453336	Remapped	1
nstd12	nsv432653	copy number variation	No	GRCh38.p12	NC_000001.11	1	118488075	118536943	Remapped	1
nstd12	nsv432664	copy number variation	No	GRCh38.p12	NC_000001.11	1	5067487	5113747	Remapped	1
nstd12	nsv432665	copy number variation	No	GRCh38.p12	NC_000001.11	1	118501291	118536943	Remapped	1
nstd12	nsv432676	copy number variation	No	GRCh38.p12	NC_000001.11	1	121430980	121549160	Remapped	1.00052
nstd12	nsv432687	copy number variation	No	GRCh38.p12	NC_000001.11	1	121430980	121549282	Remapped	1.00052
nstd12	nsv432698	copy number variation	No	GRCh38.p12	NC_000001.11	1	121442100	121549160	Remapped	1.00056
nstd12	nsv432720	copy number variation	No	GRCh38.p12	NC_000001.11	1	148539844	149064435	Remapped	0.68015
nstd12	nsv432731	copy number variation	No	GRCh38.p12	NC_000001.11	1	145707110	146068046	Remapped	0.99982
nstd12	nsv432742	copy number variation	No	GRCh38.p12	NC_000001.11	1	145707110	146039391	Remapped	0.99979
nstd12	nsv432753	copy number variation	No	GRCh38.p12	NC_000001.11	1	145707110	145864128	Remapped	1.00011
nstd12	nsv432764	copy number variation	No	GRCh38.p12	NC_000001.11	1	145258654	149556249	Remapped	3.30493
nstd12	nsv432775	copy number variation	No	GRCh38.p12	NC_000001.11	1	7003327	7081144	Remapped	1
nstd12	nsv432776	copy number variation	No	GRCh38.p12	NC_000001.11	1	148263813	148335964	Remapped	1.0021
nstd12	nsv432787	copy number variation	No	GRCh38.p12	NC_000001.11	1	145253163	148533877	Remapped	3.17591
nstd12	nsv432798	copy number variation	No	GRCh38.p12	NC_000001.11	1	143398568	145232812	Remapped	2.22062
nstd12	nsv432809	copy number variation	No	GRCh38.p12	NC_000001.11	1	143509840	143760294	Remapped	0.7509
nstd12	nsv432820	copy number variation	No	GRCh38.p12	NC_000001.11	1	143398568	145232812	Remapped	1.77564
nstd12	nsv432842	copy number variation	No	GRCh38.p12	NC_000001.11	1	143509840	143760759	Remapped	0.75126
nstd12	nsv432853	copy number variation	No	GRCh38.p12	NC_000001.11	1	143545399	143760294	Remapped	1.00008
nstd12	nsv432886	copy number variation	No	GRCh38.p12	NC_000001.11	1	16488499	16617349	Remapped	1
nstd12	nsv432920	copy number variation	No	GRCh38.p12	NC_000001.11	1	151309988	152761914	Remapped	1
nstd12	nsv432931	copy number variation	No	GRCh38.p12	NC_000001.11	1	154821842	154882579	Remapped	1
nstd12	nsv432942	copy number variation	No	GRCh38.p12	NC_000001.11	1	154845877	154930571	Remapped	1
nstd12	nsv432953	copy number variation	No	GRCh38.p12	NC_000001.11	1	154847591	154882579	Remapped	1
nstd12	nsv432964	copy number variation	No	GRCh38.p12	NC_000001.11	1	154847591	154877114	Remapped	1
nstd12	nsv432975	copy number variation	No	GRCh38.p12	NC_000001.11	1	159462137	159492137	Remapped	1
nstd12	nsv432986	copy number variation	No	GRCh38.p12	NC_000001.11	1	161251343	161703892	Remapped	1.21937
nstd12	nsv432997	copy number variation	No	GRCh38.p12	NC_000001.11	1	16488499	16632967	Remapped	1
nstd12	nsv432998	copy number variation	No	GRCh38.p12	NC_000001.11	1	161366112	161703892	Remapped	1.31757
nstd12	nsv433009	copy number variation	No	GRCh38.p12	NC_000001.11	1	161374137	161669538	Remapped	1.38038
nstd12	nsv433020	copy number variation	No	GRCh38.p12	NC_000001.11	1	161385844	161703892	Remapped	1.34405
nstd12	nsv433031	copy number variation	No	GRCh38.p12	NC_000001.11	1	161385938	161703892	Remapped	1.34419
nstd12	nsv433042	copy number variation	No	GRCh38.p12	NC_000001.11	1	161402248	161703892	Remapped	1.36968
nstd12	nsv433053	copy number variation	No	GRCh38.p12	NC_000001.11	1	161419627	161703892	Remapped	1.40135
nstd12	nsv433075	copy number variation	No	GRCh38.p12	NC_000001.11	1	161425765	161703892	Remapped	1.41388
nstd12	nsv433086	copy number variation	No	GRCh38.p12	NC_000001.11	1	161495630	161669769	Remapped	1.87748
nstd12	nsv433097	copy number variation	No	GRCh38.p12	NC_000001.11	1	161508961	161669769	Remapped	2.02477

dbVar

Database of genomic structural variation

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