dbVar data for all organisms

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Variant Placements (including Supporting Variants) for nstd195 (displaying 100 of 34258 variants)
Study ID	Variant ID	Variant Region type	Variant Call type	Method	Analysis ID	Validation	Variant samples	Assembly	Accession	Chr	Start	End	Placement Type	Remap Score
nstd195	nssv16232665		copy number variation	Sequencing	Paired-end mapping	No	B381	GRCh38.p12	NC_000001.11	1	264500	266650	Remapped	1
nstd195	nssv16232686		copy number variation	Sequencing	Paired-end mapping	No	M456	GRCh38.p12	NC_000001.11	1	628821	635571	Remapped	1
nstd195	nssv16232687		deletion	Sequencing	Paired-end mapping	No	M456	GRCh38.p12	NC_000001.11	1	790988	790989	Remapped	1
nstd195	nssv16232688		interchromosomal translocation	Sequencing	Paired-end mapping	No	M456	GRCh38.p12	NC_000001.11	1	880404	880404	Remapped	1
nstd195	nssv16232689		interchromosomal translocation	Sequencing	Paired-end mapping	No	M456	GRCh38.p12	NC_000001.11	1	880404	880404	Remapped	1
nstd195	nssv16232978		interchromosomal translocation	Sequencing	Paired-end mapping	No	B381	GRCh38.p12	NC_000001.11	1	880024	880024	Remapped	1
nstd195	nssv16232997		copy number variation	Sequencing	Paired-end mapping	No	B381	GRCh38.p12	NC_000001.11	1	882771	887121	Remapped	1
nstd195	nssv16233376		deletion	Sequencing	Paired-end mapping	No	M456	GRCh38.p12	NC_000001.11	1	790225	790226	Remapped	1
nstd195	nssv16233377		copy number variation	Sequencing	Paired-end mapping	No	M456	GRCh38.p12	NC_000001.11	1	879821	882671	Remapped	1
nstd195	nssv16233378		interchromosomal translocation	Sequencing	Paired-end mapping	No	M456	GRCh38.p12	NC_000001.11	1	880003	880003	Remapped	1
nstd195	nssv16236742		copy number variation	Sequencing	Paired-end mapping	No	M478	GRCh38.p12	NC_000001.11	1	629071	629771	Remapped	1
nstd195	nssv16236743		copy number variation	Sequencing	Paired-end mapping	No	M478	GRCh38.p12	NC_000001.11	1	879271	882721	Remapped	1
nstd195	nssv16236865		interchromosomal translocation	Sequencing	Paired-end mapping	No	M478	GRCh38.p12	NC_000001.11	1	881741	881741	Remapped	1
nstd195	nssv16236866		interchromosomal translocation	Sequencing	Paired-end mapping	No	M478	GRCh38.p12	NC_000001.11	1	881740	881740	Remapped	1
nstd195	nssv16237167		copy number variation	Sequencing	Paired-end mapping	No	M478	GRCh38.p12	NC_000001.11	1	264550	266500	Remapped	1
nstd195	nssv16237168		copy number variation	Sequencing	Paired-end mapping	No	M478	GRCh38.p12	NC_000001.11	1	885171	890921	Remapped	1
nstd195	nssv16237266		interchromosomal translocation	Sequencing	Paired-end mapping	No	M478	GRCh38.p12	NC_000001.11	1	881655	881655	Remapped	1
nstd195	nssv16238971		copy number variation	Sequencing	Paired-end mapping	No	M478	GRCh38.p12	NC_000001.11	1	631921	634871	Remapped	1
nstd195	nssv16238972		copy number variation	Sequencing	Paired-end mapping	No	M478	GRCh38.p12	NC_000001.11	1	656371	657171	Remapped	1
nstd195	nssv16238973		deletion	Sequencing	Paired-end mapping	No	M478	GRCh38.p12	NC_000001.11	1	734470	734471	Remapped	1
nstd195	nssv16238974		deletion	Sequencing	Paired-end mapping	No	M478	GRCh38.p12	NC_000001.11	1	821304	821305	Remapped	1
nstd195	nssv16239495		interchromosomal translocation	Sequencing	Paired-end mapping	No	M478	GRCh38.p12	NC_000001.11	1	870175	870175	Remapped	1
nstd195	nssv16239496		interchromosomal translocation	Sequencing	Paired-end mapping	No	M478	GRCh38.p12	NC_000001.11	1	870174	870174	Remapped	1
nstd195	nssv16239804		interchromosomal translocation	Sequencing	Paired-end mapping	No	M478	GRCh38.p12	NC_000001.11	1	879881	879881	Remapped	1
nstd195	nssv16242425		interchromosomal translocation	Sequencing	Paired-end mapping	No	M478	GRCh38.p12	NC_000001.11	1	879882	879882	Remapped	1
nstd195	nssv16243228		copy number variation	Sequencing	Paired-end mapping	No	B381	GRCh38.p12	NC_000001.11	1	604771	605871	Remapped	1
nstd195	nssv16244138		copy number variation	Sequencing	Paired-end mapping	No	B381	GRCh38.p12	NC_000001.11	1	632271	634971	Remapped	1
nstd195	nssv16245297		copy number variation	Sequencing	Paired-end mapping	No	B381	GRCh38.p12	NC_000001.11	1	628871	632221	Remapped	1
nstd195	nssv16245723		copy number variation	Sequencing	Paired-end mapping	No	B450	GRCh38.p12	NC_000001.11	1	12801	17551	Remapped	1
nstd195	nssv16245724		copy number variation	Sequencing	Paired-end mapping	No	B450	GRCh38.p12	NC_000001.11	1	19851	20551	Remapped	1
nstd195	nssv16245725		interchromosomal translocation	Sequencing	Paired-end mapping	No	B450	GRCh38.p12	NC_000001.11	1	818603	818603	Remapped	1
nstd195	nssv16245726		interchromosomal translocation	Sequencing	Paired-end mapping	No	B450	GRCh38.p12	NC_000001.11	1	861922	861922	Remapped	1
nstd195	nssv16245727		interchromosomal translocation	Sequencing	Paired-end mapping	No	B450	GRCh38.p12	NC_000001.11	1	879881	879881	Remapped	1
nstd195	nssv16246289		copy number variation	Sequencing	Paired-end mapping	No	B381	GRCh38.p12	NC_000001.11	1	656371	657171	Remapped	1
nstd195	nssv16247822		copy number variation	Sequencing	Paired-end mapping	No	B450	GRCh38.p12	NC_000001.11	1	84051	90151	Remapped	1
nstd195	nssv16247823		copy number variation	Sequencing	Paired-end mapping	No	B450	GRCh38.p12	NC_000001.11	1	628921	635821	Remapped	1
nstd195	nssv16247824		copy number variation	Sequencing	Paired-end mapping	No	B450	GRCh38.p12	NC_000001.11	1	656421	657121	Remapped	1
nstd195	nssv16247826		interchromosomal translocation	Sequencing	Paired-end mapping	No	B450	GRCh38.p12	NC_000001.11	1	818603	818603	Remapped	1
nstd195	nssv16247827		deletion	Sequencing	Paired-end mapping	No	B450	GRCh38.p12	NC_000001.11	1	820962	820963	Remapped	1
nstd195	nssv16247828		copy number variation	Sequencing	Paired-end mapping	No	B450	GRCh38.p12	NC_000001.11	1	878821	882721	Remapped	1
nstd195	nssv16247829		interchromosomal translocation	Sequencing	Paired-end mapping	No	B450	GRCh38.p12	NC_000001.11	1	879881	879881	Remapped	1
nstd195	nssv16247830		copy number variation	Sequencing	Paired-end mapping	No	B450	GRCh38.p12	NC_000001.11	1	885271	890921	Remapped	1
nstd195	nssv16247981		deletion	Sequencing	Paired-end mapping	No	B381	GRCh38.p12	NC_000001.11	1	790163	790164	Remapped	1
nstd195	nssv16248894		copy number variation	Sequencing	Paired-end mapping	No	B381	GRCh38.p12	NC_000001.11	1	879721	882721	Remapped	1
nstd195	nssv16249132		interchromosomal translocation	Sequencing	Paired-end mapping	No	B450	GRCh38.p12	NC_000001.11	1	879708	879708	Remapped	1
nstd195	nssv16249579		copy number variation	Sequencing	Paired-end mapping	No	B450	GRCh38.p12	NC_000001.11	1	265150	266700	Remapped	1
nstd195	nssv16249580		deletion	Sequencing	Paired-end mapping	No	B450	GRCh38.p12	NC_000001.11	1	820940	820941	Remapped	1
nstd195	nssv16249581		deletion	Sequencing	Paired-end mapping	No	B450	GRCh38.p12	NC_000001.11	1	831213	831214	Remapped	1
nstd195	nssv16249582		interchromosomal translocation	Sequencing	Paired-end mapping	No	B450	GRCh38.p12	NC_000001.11	1	861922	861922	Remapped	1
nstd195	nssv16250387		interchromosomal translocation	Sequencing	Paired-end mapping	No	B381	GRCh38.p12	NC_000001.11	1	880003	880003	Remapped	1
nstd195	nssv16250519		deletion	Sequencing	Paired-end mapping	No	B381	GRCh38.p12	NC_000001.11	1	820962	820963	Remapped	1
nstd195	nsv4701835	copy number variation				No		GRCh38.p12	NC_000001.11	1	265150	266700	Remapped	1
nstd195	nsv4701845	copy number variation				No		GRCh38.p12	NC_000001.11	1	631921	634871	Remapped	1
nstd195	nsv4702620	copy number variation				No		GRCh38.p12	NC_000001.11	1	885271	890921	Remapped	1
nstd195	nsv4703003	translocation				No		GRCh38.p12	NC_000001.11	1	879882	879882	Remapped	1
nstd195	nsv4703142	copy number variation				No		GRCh38.p12	NC_000001.11	1	734470	734471	Remapped	1
nstd195	nsv4703229	copy number variation				No		GRCh38.p12	NC_000001.11	1	885171	890921	Remapped	1
nstd195	nsv4703270	copy number variation				No		GRCh38.p12	NC_000001.11	1	790225	790226	Remapped	1
nstd195	nsv4703404	copy number variation				No		GRCh38.p12	NC_000001.11	1	820940	820941	Remapped	1
nstd195	nsv4703613	copy number variation				No		GRCh38.p12	NC_000001.11	1	790163	790164	Remapped	1
nstd195	nsv4703643	translocation				No		GRCh38.p12	NC_000001.11	1	879881	879881	Remapped	1
nstd195	nsv4703851	copy number variation				No		GRCh38.p12	NC_000001.11	1	656421	657121	Remapped	1
nstd195	nsv4704098	translocation				No		GRCh38.p12	NC_000001.11	1	880003	880003	Remapped	1
nstd195	nsv4705083	copy number variation				No		GRCh38.p12	NC_000001.11	1	628821	635571	Remapped	1
nstd195	nsv4705415	translocation				No		GRCh38.p12	NC_000001.11	1	881740	881740	Remapped	1
nstd195	nsv4705503	translocation				No		GRCh38.p12	NC_000001.11	1	861922	861922	Remapped	1
nstd195	nsv4705654	translocation				No		GRCh38.p12	NC_000001.11	1	881741	881741	Remapped	1
nstd195	nsv4705748	translocation				No		GRCh38.p12	NC_000001.11	1	861922	861922	Remapped	1
nstd195	nsv4706006	copy number variation				No		GRCh38.p12	NC_000001.11	1	19851	20551	Remapped	1
nstd195	nsv4706719	translocation				No		GRCh38.p12	NC_000001.11	1	870174	870174	Remapped	1
nstd195	nsv4706785	copy number variation				No		GRCh38.p12	NC_000001.11	1	879721	882721	Remapped	1
nstd195	nsv4707455	copy number variation				No		GRCh38.p12	NC_000001.11	1	821304	821305	Remapped	1
nstd195	nsv4707650	copy number variation				No		GRCh38.p12	NC_000001.11	1	264500	266650	Remapped	1
nstd195	nsv4707719	translocation				No		GRCh38.p12	NC_000001.11	1	880404	880404	Remapped	1
nstd195	nsv4708363	translocation				No		GRCh38.p12	NC_000001.11	1	881655	881655	Remapped	1
nstd195	nsv4708832	copy number variation				No		GRCh38.p12	NC_000001.11	1	790988	790989	Remapped	1
nstd195	nsv4708981	copy number variation				No		GRCh38.p12	NC_000001.11	1	12801	17551	Remapped	1
nstd195	nsv4709542	translocation				No		GRCh38.p12	NC_000001.11	1	880024	880024	Remapped	1
nstd195	nsv4709662	translocation				No		GRCh38.p12	NC_000001.11	1	880003	880003	Remapped	1
nstd195	nsv4709777	copy number variation				No		GRCh38.p12	NC_000001.11	1	656371	657171	Remapped	1
nstd195	nsv4710019	copy number variation				No		GRCh38.p12	NC_000001.11	1	604771	605871	Remapped	1
nstd195	nsv4710060	copy number variation				No		GRCh38.p12	NC_000001.11	1	879821	882671	Remapped	1
nstd195	nsv4710434	translocation				No		GRCh38.p12	NC_000001.11	1	818603	818603	Remapped	1
nstd195	nsv4710563	copy number variation				No		GRCh38.p12	NC_000001.11	1	878821	882721	Remapped	1
nstd195	nsv4710600	translocation				No		GRCh38.p12	NC_000001.11	1	880404	880404	Remapped	1
nstd195	nsv4710668	copy number variation				No		GRCh38.p12	NC_000001.11	1	820962	820963	Remapped	1
nstd195	nsv4710670	translocation				No		GRCh38.p12	NC_000001.11	1	818603	818603	Remapped	1
nstd195	nsv4710726	translocation				No		GRCh38.p12	NC_000001.11	1	870175	870175	Remapped	1
nstd195	nsv4711072	copy number variation				No		GRCh38.p12	NC_000001.11	1	831213	831214	Remapped	1
nstd195	nsv4711237	copy number variation				No		GRCh38.p12	NC_000001.11	1	628871	632221	Remapped	1
nstd195	nsv4711354	copy number variation				No		GRCh38.p12	NC_000001.11	1	632271	634971	Remapped	1
nstd195	nsv4711518	copy number variation				No		GRCh38.p12	NC_000001.11	1	629071	629771	Remapped	1
nstd195	nsv4712496	translocation				No		GRCh38.p12	NC_000001.11	1	879881	879881	Remapped	1
nstd195	nsv4712640	copy number variation				No		GRCh38.p12	NC_000001.11	1	628921	635821	Remapped	1
nstd195	nsv4712813	translocation				No		GRCh38.p12	NC_000001.11	1	879881	879881	Remapped	1
nstd195	nsv4713282	copy number variation				No		GRCh38.p12	NC_000001.11	1	879271	882721	Remapped	1
nstd195	nsv4713293	translocation				No		GRCh38.p12	NC_000001.11	1	879708	879708	Remapped	1
nstd195	nsv4714034	copy number variation				No		GRCh38.p12	NC_000001.11	1	882771	887121	Remapped	1
nstd195	nsv4715063	copy number variation				No		GRCh38.p12	NC_000001.11	1	264550	266500	Remapped	1
nstd195	nsv4715400	copy number variation				No		GRCh38.p12	NC_000001.11	1	84051	90151	Remapped	1

dbVar

Database of genomic structural variation

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