dbVar data for all organisms

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Variant Placements (including Supporting Variants) for nstd55
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
nstd55	nssv650713		deletion	Sequencing	Sequence alignment	No	114	GRCh37 (hg19)	NC_000023.10	X	139496584	139502957	Submitted genomic
nstd55	nssv650713		deletion	Sequencing	Sequence alignment	No	114	GRCh37 (hg19)	NC_000023.10	X	139496584	139502957	Submitted genomic
nstd55	nssv650713		deletion	Sequencing	Sequence alignment	No	114	GRCh38.p12	NC_000023.11	X	140414419	140420792	Remapped	1
nstd55	nssv650714		deletion	Sequencing	Sequence alignment	No	4	GRCh37 (hg19)	NC_000023.10	X	139495035	139502951	Submitted genomic
nstd55	nssv650714		deletion	Sequencing	Sequence alignment	No	4	GRCh37 (hg19)	NC_000023.10	X	139495035	139502951	Submitted genomic
nstd55	nssv650714		deletion	Sequencing	Sequence alignment	No	4	GRCh38.p12	NC_000023.11	X	140412870	140420786	Remapped	1
nstd55	nssv650715		deletion	Sequencing	Sequence alignment	No	195CA	GRCh37 (hg19)	NC_000023.10	X	139501394	139502958	Submitted genomic
nstd55	nssv650715		deletion	Sequencing	Sequence alignment	No	195CA	GRCh37 (hg19)	NC_000023.10	X	139501394	139502958	Submitted genomic
nstd55	nssv650715		deletion	Sequencing	Sequence alignment	No	195CA	GRCh38.p12	NC_000023.11	X	140419229	140420793	Remapped	1
nstd55	nssv650716		deletion	Sequencing	Sequence alignment	No	179CA	GRCh37 (hg19)	NC_000023.10	X	139502954	139503126	Submitted genomic
nstd55	nssv650716		deletion	Sequencing	Sequence alignment	No	179CA	GRCh37 (hg19)	NC_000023.10	X	139502954	139503126	Submitted genomic
nstd55	nssv650716		deletion	Sequencing	Sequence alignment	No	179CA	GRCh38.p12	NC_000023.11	X	140420789	140420961	Remapped	1
nstd55	nssv650717		deletion	Sequencing	Sequence alignment	No	GIP024	GRCh37 (hg19)	NC_000023.10	X	139494993	139502983	Submitted genomic
nstd55	nssv650717		deletion	Sequencing	Sequence alignment	No	GIP024	GRCh37 (hg19)	NC_000023.10	X	139494993	139502983	Submitted genomic
nstd55	nssv650717		deletion	Sequencing	Sequence alignment	No	GIP024	GRCh38.p12	NC_000023.11	X	140412828	140420818	Remapped	1
nstd55	nssv650718		deletion	Sequencing	Sequence alignment	No	GIP124	GRCh37 (hg19)	NC_000023.10	X	139494993	139502983	Submitted genomic
nstd55	nssv650718		deletion	Sequencing	Sequence alignment	No	GIP124	GRCh37 (hg19)	NC_000023.10	X	139494993	139502983	Submitted genomic
nstd55	nssv650718		deletion	Sequencing	Sequence alignment	No	GIP124	GRCh38.p12	NC_000023.11	X	140412828	140420818	Remapped	1
nstd55	nssv650719		deletion	Sequencing	Sequence alignment	No	GIP163	GRCh37 (hg19)	NC_000023.10	X	139494993	139502983	Submitted genomic
nstd55	nssv650719		deletion	Sequencing	Sequence alignment	No	GIP163	GRCh37 (hg19)	NC_000023.10	X	139494993	139502983	Submitted genomic
nstd55	nssv650719		deletion	Sequencing	Sequence alignment	No	GIP163	GRCh38.p12	NC_000023.11	X	140412828	140420818	Remapped	1
nstd55	nssv650720		deletion	Sequencing	Sequence alignment	No	GIP044	GRCh37 (hg19)	NC_000023.10	X	139493885	139502988	Submitted genomic
nstd55	nssv650720		deletion	Sequencing	Sequence alignment	No	GIP044	GRCh37 (hg19)	NC_000023.10	X	139493885	139502988	Submitted genomic
nstd55	nssv650720		deletion	Sequencing	Sequence alignment	No	GIP044	GRCh38.p12	NC_000023.11	X	140411720	140420823	Remapped	1
nstd55	nssv650721		deletion	Sequencing	Sequence alignment	No	PAT473	GRCh37 (hg19)	NC_000023.10	X	139494995	139502957	Submitted genomic
nstd55	nssv650721		deletion	Sequencing	Sequence alignment	No	PAT473	GRCh37 (hg19)	NC_000023.10	X	139494995	139502957	Submitted genomic
nstd55	nssv650721		deletion	Sequencing	Sequence alignment	No	PAT473	GRCh38.p12	NC_000023.11	X	140412830	140420792	Remapped	1
nstd55	nsv515477	copy number variation				No		GRCh37 (hg19)	NC_000023.10	X	139496584	139502957	Submitted genomic
nstd55	nsv515477	copy number variation				No		GRCh37 (hg19)	NC_000023.10	X	139496584	139502957	Submitted genomic
nstd55	nsv515477	copy number variation				No		GRCh38.p12	NC_000023.11	X	140414419	140420792	Remapped	1
nstd55	nsv515478	copy number variation				No		GRCh37 (hg19)	NC_000023.10	X	139495035	139502951	Submitted genomic
nstd55	nsv515478	copy number variation				No		GRCh37 (hg19)	NC_000023.10	X	139495035	139502951	Submitted genomic
nstd55	nsv515478	copy number variation				No		GRCh38.p12	NC_000023.11	X	140412870	140420786	Remapped	1
nstd55	nsv515479	copy number variation				No		GRCh37 (hg19)	NC_000023.10	X	139501394	139502958	Submitted genomic
nstd55	nsv515479	copy number variation				No		GRCh37 (hg19)	NC_000023.10	X	139501394	139502958	Submitted genomic
nstd55	nsv515479	copy number variation				No		GRCh38.p12	NC_000023.11	X	140419229	140420793	Remapped	1
nstd55	nsv515480	copy number variation				No		GRCh37 (hg19)	NC_000023.10	X	139502954	139503126	Submitted genomic
nstd55	nsv515480	copy number variation				No		GRCh37 (hg19)	NC_000023.10	X	139502954	139503126	Submitted genomic
nstd55	nsv515480	copy number variation				No		GRCh38.p12	NC_000023.11	X	140420789	140420961	Remapped	1
nstd55	nsv515481	copy number variation				No		GRCh37 (hg19)	NC_000023.10	X	139494993	139502983	Submitted genomic
nstd55	nsv515481	copy number variation				No		GRCh37 (hg19)	NC_000023.10	X	139494993	139502983	Submitted genomic
nstd55	nsv515481	copy number variation				No		GRCh38.p12	NC_000023.11	X	140412828	140420818	Remapped	1
nstd55	nsv515482	copy number variation				No		GRCh37 (hg19)	NC_000023.10	X	139493885	139502988	Submitted genomic
nstd55	nsv515482	copy number variation				No		GRCh37 (hg19)	NC_000023.10	X	139493885	139502988	Submitted genomic
nstd55	nsv515482	copy number variation				No		GRCh38.p12	NC_000023.11	X	140411720	140420823	Remapped	1
nstd55	nsv515483	copy number variation				No		GRCh37 (hg19)	NC_000023.10	X	139494995	139502957	Submitted genomic
nstd55	nsv515483	copy number variation				No		GRCh37 (hg19)	NC_000023.10	X	139494995	139502957	Submitted genomic
nstd55	nsv515483	copy number variation				No		GRCh38.p12	NC_000023.11	X	140412830	140420792	Remapped	1

dbVar

Database of genomic structural variation

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