dbVar data for all organisms

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Variant Placements (including Supporting Variants) for nstd200 (displaying 100 of 598184 variants)
Study ID	Variant ID	Variant Region type	Variant Call type	Sampleset ID	Method	Analysis ID	Validation	Assembly	Accession	Chr	Outer-Start	Start	Inner-Start	Inner-End	End	Outer-End	Placement Type	Remap Score
nstd200	nssv16311297		alu deletion	1	Sequencing	Sequence alignment	No	GRCh38.p12	NC_000001.11	1		899025			899326		Remapped	1
nstd200	nssv16311983		deletion	1	Sequencing	Sequence alignment	No	GRCh38.p12	NC_000001.11	1	816284	816285	816288	821374	821377	821378	Remapped	1
nstd200	nssv16311984		deletion	1	Sequencing	Sequence alignment	No	GRCh38.p12	NC_000001.11	1		828692			913001		Remapped	1
nstd200	nssv16311985		deletion	1	Sequencing	Sequence alignment	No	GRCh38.p12	NC_000001.11	1	831034	831062	831090	833665	833732	833742	Remapped	1
nstd200	nssv16311986		deletion	1	Sequencing	Sequence alignment	No	GRCh38.p12	NC_000001.11	1		841389			856501		Remapped	1
nstd200	nssv16311987		deletion	1	Sequencing	Sequence alignment	No	GRCh38.p12	NC_000001.11	1		853024			862929		Remapped	1
nstd200	nssv16311988		deletion	1	Sequencing	Sequence alignment	No	GRCh38.p12	NC_000001.11	1	860570	860572	860663	864982	865094		Remapped	1
nstd200	nssv16311989		deletion	1	Sequencing	Sequence alignment	No	GRCh38.p12	NC_000001.11	1	873537	873540	873584	899701	899791		Remapped	1
nstd200	nssv16311990		deletion	1	Sequencing	Sequence alignment	No	GRCh38.p12	NC_000001.11	1	886537	886538	886539	889853	889854		Remapped	1
nstd200	nssv16311991		deletion	1	Sequencing	Sequence alignment	No	GRCh38.p12	NC_000001.11	1	895394	895395	895396	899103	899104	899105	Remapped	1
nstd200	nssv16311992		deletion	1	Sequencing	Sequence alignment	No	GRCh38.p12	NC_000001.11	1	934048	934079	934110	934438	934446	934454	Remapped	1
nstd200	nssv16311993		deletion	1	Sequencing	Sequence alignment	No	GRCh38.p12	NC_000001.11	1		942912			1058985		Remapped	1
nstd200	nssv16311994		deletion	1	Sequencing	Sequence alignment	No	GRCh38.p12	NC_000001.11	1		979844			979980		Remapped	1
nstd200	nssv16311995		deletion	1	Sequencing	Sequence alignment	No	GRCh38.p12	NC_000001.11	1		985090			987643		Remapped	1
nstd200	nssv16311996		deletion	1	Sequencing	Sequence alignment	No	GRCh38.p12	NC_000001.11	1	986365	986368	986404	987754	987861	987862	Remapped	1
nstd200	nssv16311997		deletion	1	Sequencing	Sequence alignment	No	GRCh38.p12	NC_000001.11	1	1008816	1008818	1008896	1015951	1016012	1016013	Remapped	1
nstd200	nssv16311998		deletion	1	Sequencing	Sequence alignment	No	GRCh38.p12	NC_000001.11	1	1028693	1028828	1028963	1028980	1029081	1029133	Remapped	1
nstd200	nssv16311999		deletion	1	Sequencing	Sequence alignment	No	GRCh38.p12	NC_000001.11	1	1029679	1029680	1029681	1029939	1029940	1029941	Remapped	1
nstd200	nssv16312000		deletion	1	Sequencing	Sequence alignment	No	GRCh38.p12	NC_000001.11	1	1108721	1108739	1108757	1108986	1108999	1109012	Remapped	1
nstd200	nssv16312001		deletion	1	Sequencing	Sequence alignment	No	GRCh38.p12	NC_000001.11	1		1120712			1122096		Remapped	1
nstd200	nssv16383279		duplication	1	Sequencing	Sequence alignment	No	GRCh38.p12	NC_000001.11	1	786555	786558		837631	837633	837636	Remapped	1
nstd200	nssv16383280		duplication	1	Sequencing	Sequence alignment	No	GRCh38.p12	NC_000001.11	1	792441	792442		878696	878697	878698	Remapped	1
nstd200	nssv16383281		duplication	1	Sequencing	Sequence alignment	No	GRCh38.p12	NC_000001.11	1	819938	820032	820126	820918	821137	821356	Remapped	1
nstd200	nssv16383282		duplication	1	Sequencing	Sequence alignment	No	GRCh38.p12	NC_000001.11	1	820350	820512	820876	823475	823642	823809	Remapped	1
nstd200	nssv16383283		duplication	1	Sequencing	Sequence alignment	No	GRCh38.p12	NC_000001.11	1	823060	823192	823193		823577	823752	Remapped	1
nstd200	nssv16383284		duplication	1	Sequencing	Sequence alignment	No	GRCh38.p12	NC_000001.11	1		858988			929737		Remapped	1
nstd200	nssv16383285		duplication	1	Sequencing	Sequence alignment	No	GRCh38.p12	NC_000001.11	1		872210			908115		Remapped	1
nstd200	nssv16383286		duplication	1	Sequencing	Sequence alignment	No	GRCh38.p12	NC_000001.11	1		904469			904739		Remapped	1
nstd200	nssv16383287		duplication	1	Sequencing	Sequence alignment	No	GRCh38.p12	NC_000001.11	1		969321			969868		Remapped	1
nstd200	nssv16383288		duplication	1	Sequencing	Sequence alignment	No	GRCh38.p12	NC_000001.11	1	985055	985086	985089		987563	987611	Remapped	1
nstd200	nssv16383289		duplication	1	Sequencing	Sequence alignment	No	GRCh38.p12	NC_000001.11	1		1008789			1010213		Remapped	1
nstd200	nssv16383290		duplication	1	Sequencing	Sequence alignment	No	GRCh38.p12	NC_000001.11	1	1013995	1013996		1017236	1017237	1017238	Remapped	1
nstd200	nssv16383291		duplication	1	Sequencing	Sequence alignment	No	GRCh38.p12	NC_000001.11	1	1098670	1099008	1099465	1099784	1099903	1100022	Remapped	1
nstd200	nssv16398285		interchromosomal translocation	1	Sequencing	Sequence alignment	No	GRCh38.p12	NC_000001.11	1		850677			850677		Remapped	1
nstd200	nssv16409046		intrachromosomal translocation	1	Sequencing	Sequence alignment	No	GRCh38.p12	NC_000001.11	1		1025887			1025887		Remapped	1
nstd200	nssv16409046		intrachromosomal translocation	1	Sequencing	Sequence alignment	No	GRCh38.p12	NC_000001.11	1		1028193			1028193		Remapped	1
nstd200	nssv16415234		intrachromosomal translocation	1	Sequencing	Sequence alignment	No	GRCh38.p12	NC_000001.11	1		793966			793966		Remapped	1
nstd200	nssv16415234		intrachromosomal translocation	1	Sequencing	Sequence alignment	No	GRCh38.p12	NC_000001.11	1		825846			825846		Remapped	1
nstd200	nssv16415235		intrachromosomal translocation	1	Sequencing	Sequence alignment	No	GRCh38.p12	NC_000001.11	1		860719			860719		Remapped	1
nstd200	nssv16415235		intrachromosomal translocation	1	Sequencing	Sequence alignment	No	GRCh38.p12	NC_000001.11	1		873042			873042		Remapped	1
nstd200	nssv16415236		intrachromosomal translocation	1	Sequencing	Sequence alignment	No	GRCh38.p12	NC_000001.11	1		938039			938039		Remapped	1
nstd200	nssv16415236		intrachromosomal translocation	1	Sequencing	Sequence alignment	No	GRCh38.p12	NC_000001.11	1		938669			938669		Remapped	1
nstd200	nssv16415237		intrachromosomal translocation	1	Sequencing	Sequence alignment	No	GRCh38.p12	NC_000001.11	1		945428			945428		Remapped	1
nstd200	nssv16415237		intrachromosomal translocation	1	Sequencing	Sequence alignment	No	GRCh38.p12	NC_000001.11	1		960876			960876		Remapped	1
nstd200	nssv16415238		intrachromosomal translocation	1	Sequencing	Sequence alignment	No	GRCh38.p12	NC_000001.11	1		1011741			1011741		Remapped	1
nstd200	nssv16415238		intrachromosomal translocation	1	Sequencing	Sequence alignment	No	GRCh38.p12	NC_000001.11	1		1012621			1012621		Remapped	1
nstd200	nssv16415239		intrachromosomal translocation	1	Sequencing	Sequence alignment	No	GRCh38.p12	NC_000001.11	1		1087690			1087690		Remapped	1
nstd200	nssv16415239		intrachromosomal translocation	1	Sequencing	Sequence alignment	No	GRCh38.p12	NC_000001.11	1		1088113			1088113		Remapped	1
nstd200	nssv16415240		intrachromosomal translocation	1	Sequencing	Sequence alignment	No	GRCh38.p12	NC_000001.11	1		1099213			1099213		Remapped	1
nstd200	nssv16415240		intrachromosomal translocation	1	Sequencing	Sequence alignment	No	GRCh38.p12	NC_000001.11	1		1099710			1099710		Remapped	1
nstd200	nsv4772068	copy number variation					No	GRCh38.p12	NC_000001.11	1	786555	786558		837631	837633	837636	Remapped	1
nstd200	nsv4772069	copy number variation					No	GRCh38.p12	NC_000001.11	1	792441	792442		878696	878697	878698	Remapped	1
nstd200	nsv4772070	copy number variation					No	GRCh38.p12	NC_000001.11	1	819938	820032	820126	820918	821137	821356	Remapped	1
nstd200	nsv4772071	copy number variation					No	GRCh38.p12	NC_000001.11	1	820350	820512	820876	823475	823642	823809	Remapped	1
nstd200	nsv4772072	copy number variation					No	GRCh38.p12	NC_000001.11	1	823060	823192	823193		823577	823752	Remapped	1
nstd200	nsv4772073	copy number variation					No	GRCh38.p12	NC_000001.11	1		858988			929737		Remapped	1
nstd200	nsv4772074	copy number variation					No	GRCh38.p12	NC_000001.11	1		872210			908115		Remapped	1
nstd200	nsv4772075	copy number variation					No	GRCh38.p12	NC_000001.11	1		904469			904739		Remapped	1
nstd200	nsv4772076	copy number variation					No	GRCh38.p12	NC_000001.11	1		969321			969868		Remapped	1
nstd200	nsv4772077	copy number variation					No	GRCh38.p12	NC_000001.11	1	985055	985086	985089		987563	987611	Remapped	1
nstd200	nsv4772078	copy number variation					No	GRCh38.p12	NC_000001.11	1		1008789			1010213		Remapped	1
nstd200	nsv4772079	copy number variation					No	GRCh38.p12	NC_000001.11	1	1013995	1013996		1017236	1017237	1017238	Remapped	1
nstd200	nsv4772080	copy number variation					No	GRCh38.p12	NC_000001.11	1	1098670	1099008	1099465	1099784	1099903	1100022	Remapped	1
nstd200	nsv4772550	mobile element deletion					No	GRCh38.p12	NC_000001.11	1		899025			899326		Remapped	1
nstd200	nsv4782513	copy number variation					No	GRCh38.p12	NC_000001.11	1	816284	816285	816288	821374	821377	821378	Remapped	1
nstd200	nsv4782514	copy number variation					No	GRCh38.p12	NC_000001.11	1		828692			913001		Remapped	1
nstd200	nsv4782515	copy number variation					No	GRCh38.p12	NC_000001.11	1	831034	831062	831090	833665	833732	833742	Remapped	1
nstd200	nsv4782516	copy number variation					No	GRCh38.p12	NC_000001.11	1		841389			856501		Remapped	1
nstd200	nsv4782517	copy number variation					No	GRCh38.p12	NC_000001.11	1		853024			862929		Remapped	1
nstd200	nsv4782518	copy number variation					No	GRCh38.p12	NC_000001.11	1	860570	860572	860663	864982	865094		Remapped	1
nstd200	nsv4782519	copy number variation					No	GRCh38.p12	NC_000001.11	1	873537	873540	873584	899701	899791		Remapped	1
nstd200	nsv4782520	copy number variation					No	GRCh38.p12	NC_000001.11	1	886537	886538	886539	889853	889854		Remapped	1
nstd200	nsv4782521	copy number variation					No	GRCh38.p12	NC_000001.11	1	895394	895395	895396	899103	899104	899105	Remapped	1
nstd200	nsv4782522	copy number variation					No	GRCh38.p12	NC_000001.11	1	934048	934079	934110	934438	934446	934454	Remapped	1
nstd200	nsv4782523	copy number variation					No	GRCh38.p12	NC_000001.11	1		942912			1058985		Remapped	1
nstd200	nsv4782524	copy number variation					No	GRCh38.p12	NC_000001.11	1		979844			979980		Remapped	1
nstd200	nsv4782525	copy number variation					No	GRCh38.p12	NC_000001.11	1		985090			987643		Remapped	1
nstd200	nsv4782526	copy number variation					No	GRCh38.p12	NC_000001.11	1	986365	986368	986404	987754	987861	987862	Remapped	1
nstd200	nsv4782527	copy number variation					No	GRCh38.p12	NC_000001.11	1	1008816	1008818	1008896	1015951	1016012	1016013	Remapped	1
nstd200	nsv4782528	copy number variation					No	GRCh38.p12	NC_000001.11	1	1028693	1028828	1028963	1028980	1029081	1029133	Remapped	1
nstd200	nsv4782529	copy number variation					No	GRCh38.p12	NC_000001.11	1	1029679	1029680	1029681	1029939	1029940	1029941	Remapped	1
nstd200	nsv4782530	copy number variation					No	GRCh38.p12	NC_000001.11	1	1108721	1108739	1108757	1108986	1108999	1109012	Remapped	1
nstd200	nsv4782531	copy number variation					No	GRCh38.p12	NC_000001.11	1		1120712			1122096		Remapped	1
nstd200	nsv5330207	translocation					No	GRCh38.p12	NC_000001.11	1		1025887			1025887		Remapped	1
nstd200	nsv5330207	translocation					No	GRCh38.p12	NC_000001.11	1		1028193			1028193		Remapped	1
nstd200	nsv5337012	translocation					No	GRCh38.p12	NC_000001.11	1		1011741			1011741		Remapped	1
nstd200	nsv5337012	translocation					No	GRCh38.p12	NC_000001.11	1		1012621			1012621		Remapped	1
nstd200	nsv5340474	translocation					No	GRCh38.p12	NC_000001.11	1		850677			850677		Remapped	1
nstd200	nsv5340635	translocation					No	GRCh38.p12	NC_000001.11	1		1099213			1099213		Remapped	1
nstd200	nsv5340635	translocation					No	GRCh38.p12	NC_000001.11	1		1099710			1099710		Remapped	1
nstd200	nsv5341319	translocation					No	GRCh38.p12	NC_000001.11	1		945428			945428		Remapped	1
nstd200	nsv5341319	translocation					No	GRCh38.p12	NC_000001.11	1		960876			960876		Remapped	1
nstd200	nsv5343080	translocation					No	GRCh38.p12	NC_000001.11	1		860719			860719		Remapped	1
nstd200	nsv5343080	translocation					No	GRCh38.p12	NC_000001.11	1		873042			873042		Remapped	1
nstd200	nsv5344059	translocation					No	GRCh38.p12	NC_000001.11	1		938039			938039		Remapped	1
nstd200	nsv5344059	translocation					No	GRCh38.p12	NC_000001.11	1		938669			938669		Remapped	1
nstd200	nsv5344223	translocation					No	GRCh38.p12	NC_000001.11	1		793966			793966		Remapped	1
nstd200	nsv5344223	translocation					No	GRCh38.p12	NC_000001.11	1		825846			825846		Remapped	1
nstd200	nsv5345716	translocation					No	GRCh38.p12	NC_000001.11	1		1087690			1087690		Remapped	1
nstd200	nsv5345716	translocation					No	GRCh38.p12	NC_000001.11	1		1088113			1088113		Remapped	1

dbVar

Database of genomic structural variation

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