dbVar data for all organisms

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Variant Placements (including Supporting Variants) for nstd175 (displaying 100 of 25490 variants)
Study ID	Variant ID	Variant Region type	Variant Call type	Sampleset ID	Method	Analysis ID	Validation	Assembly	Accession	Chr	Start	End	Placement Type	Remap Score
nstd175	nssv15756337		deletion	1	Sequencing	Sequence alignment	No	GRCh38.p12	NC_000001.11	1	3326030	3326089	Remapped	1
nstd175	nssv15756341		insertion	1	Sequencing	Sequence alignment	No	GRCh38.p12	NC_000001.11	1	3578745	3578745	Remapped	1
nstd175	nssv15756364		insertion	1	Sequencing	Sequence alignment	No	GRCh38.p12	NC_000001.11	1	1993704	1993704	Remapped	1
nstd175	nssv15757312		deletion	1	Sequencing	Sequence alignment	No	GRCh38.p12	NC_000001.11	1	3591756	3591822	Remapped	1
nstd175	nssv15757512		deletion	1	Sequencing	Sequence alignment	No	GRCh38.p12	NC_000001.11	1	1350021	1351420	Remapped	1
nstd175	nssv15757610		insertion	1	Sequencing	Sequence alignment	No	GRCh38.p12	NC_000001.11	1	1948947	1948947	Remapped	1
nstd175	nssv15758018		insertion	1	Sequencing	Sequence alignment	No	GRCh38.p12	NC_000001.11	1	3428146	3428146	Remapped	1
nstd175	nssv15758204		insertion	1	Sequencing	Sequence alignment	No	GRCh38.p12	NC_000001.11	1	3042652	3042652	Remapped	1
nstd175	nssv15758475		deletion	1	Sequencing	Sequence alignment	No	GRCh38.p12	NC_000001.11	1	2142322	2142407	Remapped	1
nstd175	nssv15758711		insertion	1	Sequencing	Sequence alignment	No	GRCh38.p12	NC_000001.11	1	998767	998767	Remapped	1
nstd175	nssv15759372		insertion	1	Sequencing	Sequence alignment	No	GRCh38.p12	NC_000001.11	1	2859488	2859488	Remapped	1
nstd175	nssv15759625		insertion	1	Sequencing	Sequence alignment	No	GRCh38.p12	NC_000001.11	1	1382230	1382230	Remapped	1
nstd175	nssv15759802		insertion	1	Sequencing	Sequence alignment	No	GRCh38.p12	NC_000001.11	1	2019220	2019220	Remapped	1
nstd175	nssv15759913		insertion	1	Sequencing	Sequence alignment	No	GRCh38.p12	NC_000001.11	1	2085727	2085727	Remapped	1
nstd175	nssv15759934		insertion	1	Sequencing	Sequence alignment	No	GRCh38.p12	NC_000001.11	1	2147063	2147063	Remapped	1
nstd175	nssv15760006		insertion	1	Sequencing	Sequence alignment	No	GRCh38.p12	NC_000001.11	1	1565630	1565630	Remapped	1
nstd175	nssv15760182		insertion	1	Sequencing	Sequence alignment	No	GRCh38.p12	NC_000001.11	1	3587840	3587840	Remapped	1
nstd175	nssv15761031		insertion	1	Sequencing	Sequence alignment	No	GRCh38.p12	NC_000001.11	1	2325105	2325105	Remapped	1
nstd175	nssv15761077		deletion	1	Sequencing	Sequence alignment	No	GRCh38.p12	NC_000001.11	1	2949524	2949671	Remapped	1
nstd175	nssv15761137		insertion	1	Sequencing	Sequence alignment	No	GRCh38.p12	NC_000001.11	1	1929363	1929363	Remapped	1
nstd175	nssv15761588		insertion	1	Sequencing	Sequence alignment	No	GRCh38.p12	NC_000001.11	1	976686	976686	Remapped	1
nstd175	nssv15761675		deletion	1	Sequencing	Sequence alignment	No	GRCh38.p12	NC_000001.11	1	2110021	2110116	Remapped	1
nstd175	nssv15761809		insertion	1	Sequencing	Sequence alignment	No	GRCh38.p12	NC_000001.11	1	996254	996254	Remapped	1
nstd175	nssv15762044		insertion	1	Sequencing	Sequence alignment	No	GRCh38.p12	NC_000001.11	1	2522689	2522689	Remapped	1
nstd175	nssv15762072		insertion	1	Sequencing	Sequence alignment	No	GRCh38.p12	NC_000001.11	1	3176047	3176047	Remapped	1
nstd175	nssv15762229		insertion	1	Sequencing	Sequence alignment	No	GRCh38.p12	NC_000001.11	1	3260742	3260742	Remapped	1
nstd175	nssv15762340		insertion	1	Sequencing	Sequence alignment	No	GRCh38.p12	NC_000001.11	1	2848785	2848785	Remapped	1
nstd175	nssv15762576		insertion	1	Sequencing	Sequence alignment	No	GRCh38.p12	NC_000001.11	1	3351517	3351517	Remapped	1
nstd175	nssv15762582		insertion	1	Sequencing	Sequence alignment	No	GRCh38.p12	NC_000001.11	1	3477293	3477293	Remapped	1
nstd175	nssv15762642		insertion	1	Sequencing	Sequence alignment	No	GRCh38.p12	NC_000001.11	1	3037784	3037784	Remapped	1
nstd175	nssv15762869		deletion	1	Sequencing	Sequence alignment	No	GRCh38.p12	NC_000001.11	1	1717604	1717655	Remapped	1
nstd175	nssv15762904		deletion	1	Sequencing	Sequence alignment	No	GRCh38.p12	NC_000001.11	1	2262030	2262100	Remapped	1
nstd175	nssv15763067		insertion	1	Sequencing	Sequence alignment	No	GRCh38.p12	NC_000001.11	1	3596423	3596423	Remapped	1
nstd175	nssv15763310		deletion	1	Sequencing	Sequence alignment	No	GRCh38.p12	NC_000001.11	1	2772674	2772838	Remapped	1
nstd175	nssv15763531		deletion	1	Sequencing	Sequence alignment	No	GRCh38.p12	NC_000001.11	1	2592353	2592560	Remapped	1
nstd175	nssv15763642		insertion	1	Sequencing	Sequence alignment	No	GRCh38.p12	NC_000001.11	1	1068824	1068824	Remapped	1
nstd175	nssv15764540		deletion	1	Sequencing	Sequence alignment	No	GRCh38.p12	NC_000001.11	1	964542	964612	Remapped	1
nstd175	nssv15765368		insertion	1	Sequencing	Sequence alignment	No	GRCh38.p12	NC_000001.11	1	1924223	1924223	Remapped	1
nstd175	nssv15765417		deletion	1	Sequencing	Sequence alignment	No	GRCh38.p12	NC_000001.11	1	1666974	1667141	Remapped	1
nstd175	nssv15765897		deletion	1	Sequencing	Sequence alignment	No	GRCh38.p12	NC_000001.11	1	3287565	3287662	Remapped	1
nstd175	nssv15766027		deletion	1	Sequencing	Sequence alignment	No	GRCh38.p12	NC_000001.11	1	1934205	1934802	Remapped	1
nstd175	nssv15766352		deletion	1	Sequencing	Sequence alignment	No	GRCh38.p12	NC_000001.11	1	2974672	2974739	Remapped	1
nstd175	nssv15766620		deletion	1	Sequencing	Sequence alignment	No	GRCh38.p12	NC_000001.11	1	2459426	2459490	Remapped	1
nstd175	nssv15766633		deletion	1	Sequencing	Sequence alignment	No	GRCh38.p12	NC_000001.11	1	3345757	3345823	Remapped	1
nstd175	nssv15766703		insertion	1	Sequencing	Sequence alignment	No	GRCh38.p12	NC_000001.11	1	2212194	2212194	Remapped	1
nstd175	nssv15767007		insertion	1	Sequencing	Sequence alignment	No	GRCh38.p12	NC_000001.11	1	2602115	2602115	Remapped	1
nstd175	nssv15767805		insertion	1	Sequencing	Sequence alignment	No	GRCh38.p12	NC_000001.11	1	1065313	1065313	Remapped	1
nstd175	nssv15768322		insertion	1	Sequencing	Sequence alignment	No	GRCh38.p12	NC_000001.11	1	2401406	2401406	Remapped	1
nstd175	nssv15768392		insertion	1	Sequencing	Sequence alignment	No	GRCh38.p12	NC_000001.11	1	1543795	1543795	Remapped	1
nstd175	nssv15768495		deletion	1	Sequencing	Sequence alignment	No	GRCh38.p12	NC_000001.11	1	2851919	2852127	Remapped	1
nstd175	nsv4443982	insertion					No	GRCh38.p12	NC_000001.11	1	2147063	2147063	Remapped	1
nstd175	nsv4443983	insertion					No	GRCh38.p12	NC_000001.11	1	2212194	2212194	Remapped	1
nstd175	nsv4443984	insertion					No	GRCh38.p12	NC_000001.11	1	2325105	2325105	Remapped	1
nstd175	nsv4443985	insertion					No	GRCh38.p12	NC_000001.11	1	2401406	2401406	Remapped	1
nstd175	nsv4443986	insertion					No	GRCh38.p12	NC_000001.11	1	2522689	2522689	Remapped	1
nstd175	nsv4443987	insertion					No	GRCh38.p12	NC_000001.11	1	2602115	2602115	Remapped	1
nstd175	nsv4443988	insertion					No	GRCh38.p12	NC_000001.11	1	2848785	2848785	Remapped	1
nstd175	nsv4443989	insertion					No	GRCh38.p12	NC_000001.11	1	2859488	2859488	Remapped	1
nstd175	nsv4443990	insertion					No	GRCh38.p12	NC_000001.11	1	3037784	3037784	Remapped	1
nstd175	nsv4444176	insertion					No	GRCh38.p12	NC_000001.11	1	976686	976686	Remapped	1
nstd175	nsv4444177	insertion					No	GRCh38.p12	NC_000001.11	1	996254	996254	Remapped	1
nstd175	nsv4444178	insertion					No	GRCh38.p12	NC_000001.11	1	998767	998767	Remapped	1
nstd175	nsv4444179	insertion					No	GRCh38.p12	NC_000001.11	1	1065313	1065313	Remapped	1
nstd175	nsv4444180	insertion					No	GRCh38.p12	NC_000001.11	1	1068824	1068824	Remapped	1
nstd175	nsv4444226	insertion					No	GRCh38.p12	NC_000001.11	1	1382230	1382230	Remapped	1
nstd175	nsv4444227	insertion					No	GRCh38.p12	NC_000001.11	1	1543795	1543795	Remapped	1
nstd175	nsv4444228	insertion					No	GRCh38.p12	NC_000001.11	1	1565630	1565630	Remapped	1
nstd175	nsv4444229	insertion					No	GRCh38.p12	NC_000001.11	1	1924223	1924223	Remapped	1
nstd175	nsv4444230	insertion					No	GRCh38.p12	NC_000001.11	1	1929363	1929363	Remapped	1
nstd175	nsv4444231	insertion					No	GRCh38.p12	NC_000001.11	1	1948947	1948947	Remapped	1
nstd175	nsv4444232	insertion					No	GRCh38.p12	NC_000001.11	1	1993704	1993704	Remapped	1
nstd175	nsv4444233	insertion					No	GRCh38.p12	NC_000001.11	1	2019220	2019220	Remapped	1
nstd175	nsv4444234	insertion					No	GRCh38.p12	NC_000001.11	1	2085727	2085727	Remapped	1
nstd175	nsv4444317	insertion					No	GRCh38.p12	NC_000001.11	1	3042652	3042652	Remapped	1
nstd175	nsv4444318	insertion					No	GRCh38.p12	NC_000001.11	1	3176047	3176047	Remapped	1
nstd175	nsv4444319	insertion					No	GRCh38.p12	NC_000001.11	1	3260742	3260742	Remapped	1
nstd175	nsv4444320	insertion					No	GRCh38.p12	NC_000001.11	1	3351517	3351517	Remapped	1
nstd175	nsv4444321	insertion					No	GRCh38.p12	NC_000001.11	1	3428146	3428146	Remapped	1
nstd175	nsv4444322	insertion					No	GRCh38.p12	NC_000001.11	1	3477293	3477293	Remapped	1
nstd175	nsv4444323	insertion					No	GRCh38.p12	NC_000001.11	1	3578745	3578745	Remapped	1
nstd175	nsv4444324	insertion					No	GRCh38.p12	NC_000001.11	1	3587840	3587840	Remapped	1
nstd175	nsv4444325	insertion					No	GRCh38.p12	NC_000001.11	1	3596423	3596423	Remapped	1
nstd175	nsv4448712	copy number variation					No	GRCh38.p12	NC_000001.11	1	1717604	1717655	Remapped	1
nstd175	nsv4448713	copy number variation					No	GRCh38.p12	NC_000001.11	1	1934205	1934802	Remapped	1
nstd175	nsv4448714	copy number variation					No	GRCh38.p12	NC_000001.11	1	2110021	2110116	Remapped	1
nstd175	nsv4448715	copy number variation					No	GRCh38.p12	NC_000001.11	1	2142322	2142407	Remapped	1
nstd175	nsv4448716	copy number variation					No	GRCh38.p12	NC_000001.11	1	2262030	2262100	Remapped	1
nstd175	nsv4448717	copy number variation					No	GRCh38.p12	NC_000001.11	1	2459426	2459490	Remapped	1
nstd175	nsv4448718	copy number variation					No	GRCh38.p12	NC_000001.11	1	2592353	2592560	Remapped	1
nstd175	nsv4448719	copy number variation					No	GRCh38.p12	NC_000001.11	1	2772674	2772838	Remapped	1
nstd175	nsv4448720	copy number variation					No	GRCh38.p12	NC_000001.11	1	2851919	2852127	Remapped	1
nstd175	nsv4449079	copy number variation					No	GRCh38.p12	NC_000001.11	1	2949524	2949671	Remapped	1
nstd175	nsv4449080	copy number variation					No	GRCh38.p12	NC_000001.11	1	2974672	2974739	Remapped	1
nstd175	nsv4449081	copy number variation					No	GRCh38.p12	NC_000001.11	1	3287565	3287662	Remapped	1
nstd175	nsv4449082	copy number variation					No	GRCh38.p12	NC_000001.11	1	3326030	3326089	Remapped	1
nstd175	nsv4449083	copy number variation					No	GRCh38.p12	NC_000001.11	1	3345757	3345823	Remapped	1
nstd175	nsv4449084	copy number variation					No	GRCh38.p12	NC_000001.11	1	3591756	3591822	Remapped	1
nstd175	nsv4449249	copy number variation					No	GRCh38.p12	NC_000001.11	1	1666974	1667141	Remapped	1
nstd175	nsv4449250	copy number variation					No	GRCh38.p12	NC_000001.11	1	1350021	1351420	Remapped	1
nstd175	nsv4449251	copy number variation					No	GRCh38.p12	NC_000001.11	1	964542	964612	Remapped	1

dbVar

Database of genomic structural variation

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