dbVar data for all organisms

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Variant Placements (including Supporting Variants) for nstd72
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
nstd72	nssv2995876		deletion	Sequencing	Sequence alignment	No	242	GRCh37 (hg19)	NC_000023.10	X	1333547	1654735	Submitted genomic
nstd72	nssv2995876		deletion	Sequencing	Sequence alignment	No	242	GRCh37 (hg19)	NC_000023.10	X	1333547	1654735	Submitted genomic
nstd72	nssv2995876		deletion	Sequencing	Sequence alignment	No	242	GRCh38.p12	NC_000023.11	X	1214654	1535842	Remapped	1
nstd72	nssv2995877		deletion	Sequencing	Sequence alignment	No	365	GRCh37 (hg19)	NC_000023.10	X	1331659	1655360	Submitted genomic
nstd72	nssv2995877		deletion	Sequencing	Sequence alignment	No	365	GRCh37 (hg19)	NC_000023.10	X	1331659	1655360	Submitted genomic
nstd72	nssv2995877		deletion	Sequencing	Sequence alignment	No	365	GRCh38.p12	NC_000023.11	X	1212766	1536467	Remapped	1
nstd72	nssv2995878		deletion	Sequencing	Sequence alignment	No	379	GRCh37 (hg19)	NC_000023.10	X	1333753	1655364	Submitted genomic
nstd72	nssv2995878		deletion	Sequencing	Sequence alignment	No	379	GRCh37 (hg19)	NC_000023.10	X	1333753	1655364	Submitted genomic
nstd72	nssv2995878		deletion	Sequencing	Sequence alignment	No	379	GRCh38.p12	NC_000023.11	X	1214860	1536471	Remapped	1
nstd72	nssv2995879		deletion	Sequencing	Sequence alignment	No	873	GRCh37 (hg19)	NC_000023.10	X	1333752	1655498	Submitted genomic
nstd72	nssv2995879		deletion	Sequencing	Sequence alignment	No	873	GRCh37 (hg19)	NC_000023.10	X	1333752	1655498	Submitted genomic
nstd72	nssv2995879		deletion	Sequencing	Sequence alignment	No	873	GRCh38.p12	NC_000023.11	X	1214859	1536605	Remapped	1
nstd72	nssv2995880		deletion	Sequencing	Sequence alignment	No	961	GRCh37 (hg19)	NC_000023.10	X	1331650	1654735	Submitted genomic
nstd72	nssv2995880		deletion	Sequencing	Sequence alignment	No	961	GRCh37 (hg19)	NC_000023.10	X	1331650	1654735	Submitted genomic
nstd72	nssv2995880		deletion	Sequencing	Sequence alignment	No	961	GRCh38.p12	NC_000023.11	X	1212757	1535842	Remapped	1
nstd72	nsv949747	copy number variation				No		GRCh37 (hg19)	NC_000023.10	X	1333547	1654735	Submitted genomic
nstd72	nsv949747	copy number variation				No		GRCh37 (hg19)	NC_000023.10	X	1333547	1654735	Submitted genomic
nstd72	nsv949747	copy number variation				No		GRCh38.p12	NC_000023.11	X	1214654	1535842	Remapped	1
nstd72	nsv949748	copy number variation				No		GRCh37 (hg19)	NC_000023.10	X	1331659	1655360	Submitted genomic
nstd72	nsv949748	copy number variation				No		GRCh37 (hg19)	NC_000023.10	X	1331659	1655360	Submitted genomic
nstd72	nsv949748	copy number variation				No		GRCh38.p12	NC_000023.11	X	1212766	1536467	Remapped	1
nstd72	nsv949749	copy number variation				No		GRCh37 (hg19)	NC_000023.10	X	1333753	1655364	Submitted genomic
nstd72	nsv949749	copy number variation				No		GRCh37 (hg19)	NC_000023.10	X	1333753	1655364	Submitted genomic
nstd72	nsv949749	copy number variation				No		GRCh38.p12	NC_000023.11	X	1214860	1536471	Remapped	1
nstd72	nsv949750	copy number variation				No		GRCh37 (hg19)	NC_000023.10	X	1333752	1655498	Submitted genomic
nstd72	nsv949750	copy number variation				No		GRCh37 (hg19)	NC_000023.10	X	1333752	1655498	Submitted genomic
nstd72	nsv949750	copy number variation				No		GRCh38.p12	NC_000023.11	X	1214859	1536605	Remapped	1
nstd72	nsv949751	copy number variation				No		GRCh37 (hg19)	NC_000023.10	X	1331650	1654735	Submitted genomic
nstd72	nsv949751	copy number variation				No		GRCh37 (hg19)	NC_000023.10	X	1331650	1654735	Submitted genomic
nstd72	nsv949751	copy number variation				No		GRCh38.p12	NC_000023.11	X	1212757	1535842	Remapped	1

dbVar

Database of genomic structural variation

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