dbVar data for all organisms

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Variant Placements for nstd143
Study ID	Variant ID	Variant Region type	Validation	Assembly	Accession	Chr	Start	End	Placement Type	Remap Score
nstd143	nsv3067136	copy number variation	No	GRCh37 (hg19)	NC_000016.9	16	97615	299525	Submitted genomic
nstd143	nsv3067136	copy number variation	No	GRCh38.p12	NC_000016.10	16	47615	249526	Remapped	1
nstd143	nsv3067137	copy number variation	No	GRCh37 (hg19)	NC_000016.9	16	208663	235974	Submitted genomic
nstd143	nsv3067137	copy number variation	No	GRCh37 (hg19)	NC_000016.9	16	208663	235974	Submitted genomic
nstd143	nsv3067137	copy number variation	No	GRCh38.p12	NC_000016.10	16	158664	185975	Remapped	1
nstd143	nsv3067138	copy number variation	No	GRCh37 (hg19)	NC_000016.9	16	215125	284579	Submitted genomic
nstd143	nsv3067138	copy number variation	No	GRCh37 (hg19)	NC_000016.9	16	215125	284579	Submitted genomic
nstd143	nsv3067138	copy number variation	No	GRCh38.p12	NC_000016.10	16	165126	234580	Remapped	1
nstd143	nsv3067139	copy number variation	No	GRCh37 (hg19)	NC_000016.9	16	215144	236065	Submitted genomic
nstd143	nsv3067139	copy number variation	No	GRCh37 (hg19)	NC_000016.9	16	215144	236065	Submitted genomic
nstd143	nsv3067139	copy number variation	No	GRCh38.p12	NC_000016.10	16	165145	186066	Remapped	1
nstd143	nsv3067140	copy number variation	No	GRCh37 (hg19)	NC_000016.9	16	221260	252033	Submitted genomic
nstd143	nsv3067140	copy number variation	No	GRCh37 (hg19)	NC_000016.9	16	221260	252033	Submitted genomic
nstd143	nsv3067140	copy number variation	No	GRCh38.p12	NC_000016.10	16	171261	202034	Remapped	1
nstd143	nsv3067123	copy number variation	No	GRCh37 (hg19)	NC_000016.9	16	222201	227178	Submitted genomic
nstd143	nsv3067123	copy number variation	No	GRCh37 (hg19)	NC_000016.9	16	222201	227178	Submitted genomic
nstd143	nsv3067123	copy number variation	No	GRCh38.p12	NC_000016.10	16	172202	177179	Remapped	1
nstd143	nsv3067124	copy number variation	No	GRCh37 (hg19)	NC_000016.9	16	227121	228400	Submitted genomic
nstd143	nsv3067124	copy number variation	No	GRCh37 (hg19)	NC_000016.9	16	227121	228400	Submitted genomic
nstd143	nsv3067124	copy number variation	No	GRCh38.p12	NC_000016.10	16	177122	178401	Remapped	1
nstd143	nsv3067125	copy number variation	No	GRCh37 (hg19)	NC_000016.9	16	123895	245125	Submitted genomic
nstd143	nsv3067125	copy number variation	No	GRCh37 (hg19)	NC_000016.9	16	123895	245125	Submitted genomic
nstd143	nsv3067125	copy number variation	No	GRCh38.p12	NC_000016.10	16	73897	195126	Remapped	0.99999
nstd143	nsv3067126	copy number variation	No	GRCh37 (hg19)	NC_000016.9	16	155381	290220	Submitted genomic
nstd143	nsv3067126	copy number variation	No	GRCh37 (hg19)	NC_000016.9	16	155381	290220	Submitted genomic
nstd143	nsv3067126	copy number variation	No	GRCh38.p12	NC_000016.10	16	105383	240221	Remapped	0.99999
nstd143	nsv3067127	complex substitution	No	GRCh37 (hg19)	NC_000016.9	16	94455	281325	Submitted genomic
nstd143	nsv3067127	complex substitution	No	GRCh37 (hg19)	NC_000016.9	16	94455	281325	Submitted genomic
nstd143	nsv3067127	complex substitution	No	GRCh38.p12	NC_000016.10	16	44455	231326	Remapped	1.00001
nstd143	nsv3067128	copy number variation	No	GRCh37 (hg19)	NC_000016.9	16	97115	175257	Submitted genomic
nstd143	nsv3067128	copy number variation	No	GRCh37 (hg19)	NC_000016.9	16	97115	175257	Submitted genomic
nstd143	nsv3067128	copy number variation	No	GRCh38.p12	NC_000016.10	16	47115	125258	Remapped	1.00001
nstd143	nsv3067129	copy number variation	No	GRCh37 (hg19)	NC_000011.9	11	5217204	5285011	Submitted genomic
nstd143	nsv3067129	copy number variation	No	GRCh37 (hg19)	NC_000011.9	11	5217204	5285011	Submitted genomic
nstd143	nsv3067129	copy number variation	No	GRCh38.p12	NC_000011.10	11	5195974	5263781	Remapped	1
nstd143	nsv3067130	copy number variation	No	GRCh37 (hg19)	NC_000016.9	16	196190	258010	Submitted genomic
nstd143	nsv3067130	copy number variation	No	GRCh37 (hg19)	NC_000016.9	16	196190	258010	Submitted genomic
nstd143	nsv3067130	copy number variation	No	GRCh38.p12	NC_000016.10	16	146191	208011	Remapped	1
nstd143	nsv3067131	copy number variation	No	GRCh37 (hg19)	NC_000011.9	11	5135464	5254173	Submitted genomic
nstd143	nsv3067131	copy number variation	No	GRCh37 (hg19)	NC_000011.9	11	5135464	5254173	Submitted genomic
nstd143	nsv3067131	copy number variation	No	GRCh38.p12	NC_000011.10	11	5114234	5232943	Remapped	1
nstd143	nsv3067132	copy number variation	No	GRCh37 (hg19)	NC_000011.9	11	5157109	5361649	Submitted genomic
nstd143	nsv3067132	copy number variation	No	GRCh37 (hg19)	NC_000011.9	11	5157109	5361649	Submitted genomic
nstd143	nsv3067132	copy number variation	No	GRCh38.p12	NC_000011.10	11	5135879	5340419	Remapped	1
nstd143	nsv3067133	copy number variation	No	GRCh37 (hg19)	NC_000011.9	11	5247824	5255222	Submitted genomic
nstd143	nsv3067133	copy number variation	No	GRCh37 (hg19)	NC_000011.9	11	5247824	5255222	Submitted genomic
nstd143	nsv3067133	copy number variation	No	GRCh38.p12	NC_000011.10	11	5226594	5233992	Remapped	1
nstd143	nsv3067134	copy number variation	No	GRCh37 (hg19)	NC_000016.9	16	71955	235250	Submitted genomic
nstd143	nsv3067134	copy number variation	No	GRCh37 (hg19)	NC_000016.9	16	71955	235250	Submitted genomic
nstd143	nsv3067134	copy number variation	No	GRCh38.p12	NC_000016.10	16	21955	185251	Remapped	1.00001
nstd143	nsv3067135	copy number variation	No	GRCh37 (hg19)	NC_000016.9	16	84105	238055	Submitted genomic
nstd143	nsv3067135	copy number variation	No	GRCh37 (hg19)	NC_000016.9	16	84105	238055	Submitted genomic
nstd143	nsv3067135	copy number variation	No	GRCh38.p12	NC_000016.10	16	34105	188056	Remapped	1.00001
nstd143	nsv3067136	copy number variation	No	GRCh37 (hg19)	NC_000016.9	16	97615	299525	Submitted genomic

dbVar

Database of genomic structural variation

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