dbVar data for all organisms

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Variant Placements (including Supporting Variants) for nstd190 (displaying 100 of 482 variants)
Study ID	Variant ID	Variant Region type	Variant Call type	Sampleset ID	Method	Analysis ID	Validation	Assembly	Accession	Chr	Inner-Start	Inner-End	Placement Type	Remap Score
nstd190	nssv16211534		deletion	1	SNP array	SNP genotyping analysis	No	GRCh38.p12	NC_000015.10	15	19839089	22308242	Remapped	0.80138
nstd190	nssv16211535		deletion	1	SNP array	SNP genotyping analysis	No	GRCh38.p12	NC_000015.10	15	19839089	22308242	Remapped	0.79551
nstd190	nssv16211536		deletion	1	SNP array	SNP genotyping analysis	No	GRCh38.p12	NC_000015.10	15	19839089	22308242	Remapped	0.7855
nstd190	nssv16211537		deletion	1	SNP array	SNP genotyping analysis	No	GRCh38.p12	NC_000015.10	15	19839089	26062029	Remapped	0.99363
nstd190	nssv16211538		deletion	1	SNP array	SNP genotyping analysis	No	GRCh38.p12	NC_000015.10	15	20007545	22308242	Remapped	0.75675
nstd190	nssv16211539		deletion	1	SNP array	SNP genotyping analysis	No	GRCh38.p12	NC_000015.10	15	20013263	22308242	Remapped	0.79818
nstd190	nssv16211540		deletion	1	SNP array	SNP genotyping analysis	No	GRCh38.p12	NC_000015.10	15	20013263	22308242	Remapped	0.78948
nstd190	nssv16211541		deletion	1	SNP array	SNP genotyping analysis	No	GRCh38.p12	NC_000015.10	15	20013263	22308242	Remapped	0.77867
nstd190	nssv16211542		deletion	1	SNP array	SNP genotyping analysis	No	GRCh38.p12	NC_000015.10	15	20013263	22308242	Remapped	0.75629
nstd190	nssv16211543		deletion	1	SNP array	SNP genotyping analysis	No	GRCh38.p12	NC_000015.10	15	20028295	22308242	Remapped	0.75508
nstd190	nssv16211544		deletion	1	SNP array	SNP genotyping analysis	No	GRCh38.p12	NC_000015.10	15	20028295	23422945	Remapped	0.98838
nstd190	nssv16211545		deletion	1	SNP array	SNP genotyping analysis	No	GRCh38.p12	NC_000015.10	15	20343543	22308242	Remapped	0.77199
nstd190	nssv16211546		deletion	1	SNP array	SNP genotyping analysis	No	GRCh38.p12	NC_000015.10	15	20343543	22308242	Remapped	0.7445
nstd190	nssv16211547		deletion	1	SNP array	SNP genotyping analysis	No	GRCh38.p12	NC_000015.10	15	20343543	22308242	Remapped	0.72653
nstd190	nssv16211548		deletion	1	SNP array	SNP genotyping analysis	No	GRCh38.p12	NC_000015.10	15	20343543	23386710	Remapped	0.98706
nstd190	nssv16211549		deletion	1	SNP array	SNP genotyping analysis	No	GRCh38.p12	NC_000015.10	15	20343543	23415423	Remapped	0.98718
nstd190	nssv16211550		deletion	1	SNP array	SNP genotyping analysis	No	GRCh38.p12	NC_000015.10	15	20379951	22308242	Remapped	0.75909
nstd190	nssv16211551		deletion	1	SNP array	SNP genotyping analysis	No	GRCh38.p12	NC_000015.10	15	20379951	22308242	Remapped	0.72279
nstd190	nssv16211552		deletion	1	SNP array	SNP genotyping analysis	No	GRCh38.p12	NC_000015.10	15	20343543	22308242	Remapped	0.76249
nstd190	nssv16211553		deletion	1	SNP array	SNP genotyping analysis	No	GRCh38.p12	NC_000015.10	15	20861099	22308242	Remapped	0.71381
nstd190	nssv16211554		deletion	1	SNP array	SNP genotyping analysis	No	GRCh38.p12	NC_000015.10	15	20861099	22308242	Remapped	0.70282
nstd190	nssv16211555		deletion	1	SNP array	SNP genotyping analysis	No	GRCh38.p12	NC_000015.10	15	20057775	22308242	Remapped	0.75266
nstd190	nssv16211556		deletion	1	SNP array	SNP genotyping analysis	No	GRCh38.p12	NC_000015.10	15	20861099	22308242	Remapped	0.68931
nstd190	nssv16211557		deletion	1	SNP array	SNP genotyping analysis	No	GRCh38.p12	NC_000015.10	15	20861099	22308242	Remapped	0.68219
nstd190	nssv16211558		deletion	1	SNP array	SNP genotyping analysis	No	GRCh38.p12	NC_000015.10	15	20861099	22308242	Remapped	0.67162
nstd190	nssv16211559		deletion	1	SNP array	SNP genotyping analysis	No	GRCh38.p12	NC_000015.10	15	20861099	22308242	Remapped	0.66182
nstd190	nssv16211560		deletion	1	SNP array	SNP genotyping analysis	No	GRCh38.p12	NC_000015.10	15	20861099	23386710	Remapped	0.98448
nstd190	nssv16211561		deletion	1	SNP array	SNP genotyping analysis	No	GRCh38.p12	NC_000015.10	15	20944756	22308242	Remapped	0.7015
nstd190	nssv16211562		deletion	1	SNP array	SNP genotyping analysis	No	GRCh38.p12	NC_000015.10	15	20944756	22308242	Remapped	0.69586
nstd190	nssv16211563		deletion	1	SNP array	SNP genotyping analysis	No	GRCh38.p12	NC_000015.10	15	20944756	22308242	Remapped	0.69024
nstd190	nssv16211564		deletion	1	SNP array	SNP genotyping analysis	No	GRCh38.p12	NC_000015.10	15	20944756	22308242	Remapped	0.6857
nstd190	nssv16211565		deletion	1	SNP array	SNP genotyping analysis	No	GRCh38.p12	NC_000015.10	15	20013263	23386710	Remapped	0.98831
nstd190	nssv16211566		deletion	1	SNP array	SNP genotyping analysis	No	GRCh38.p12	NC_000015.10	15	20944756	22308242	Remapped	0.68238
nstd190	nssv16211567		deletion	1	SNP array	SNP genotyping analysis	No	GRCh38.p12	NC_000015.10	15	20944756	22308242	Remapped	0.67642
nstd190	nssv16211568		deletion	1	SNP array	SNP genotyping analysis	No	GRCh38.p12	NC_000015.10	15	20944756	22308242	Remapped	0.66914
nstd190	nssv16211569		deletion	1	SNP array	SNP genotyping analysis	No	GRCh38.p12	NC_000015.10	15	20944756	22308242	Remapped	0.65835
nstd190	nssv16211570		deletion	1	SNP array	SNP genotyping analysis	No	GRCh38.p12	NC_000015.10	15	20944756	22308242	Remapped	0.65485
nstd190	nssv16211571		deletion	1	SNP array	SNP genotyping analysis	No	GRCh38.p12	NC_000015.10	15	20007545	22308242	Remapped	0.7791
nstd190	nssv16211572		deletion	1	SNP array	SNP genotyping analysis	No	GRCh38.p12	NC_000015.10	15	20944756	22308242	Remapped	0.64837
nstd190	nssv16211573		deletion	1	SNP array	SNP genotyping analysis	No	GRCh38.p12	NC_000015.10	15	20944756	23653247	Remapped	0.98551
nstd190	nssv16211575		deletion	1	SNP array	SNP genotyping analysis	No	GRCh38.p12	NC_000015.10	15	19839089	22308242	Remapped	0.76952
nstd190	nssv16211580		deletion	1	SNP array	SNP genotyping analysis	No	GRCh38.p12	NC_000015.10	15	19839089	22308242	Remapped	0.798
nstd190	nssv16211581		deletion	1	SNP array	SNP genotyping analysis	No	GRCh38.p12	NC_000015.10	15	20534837	22308242	Remapped	0.70571
nstd190	nssv16211584		deletion	1	SNP array	SNP genotyping analysis	No	GRCh38.p12	NC_000015.10	15	19839089	27906894	Remapped	0.99508
nstd190	nssv16211611		deletion	1	SNP array	SNP genotyping analysis	No	GRCh38.p12	NC_000015.10	15	20861099	22308242	Remapped	0.69515
nstd190	nssv16211612		deletion	1	SNP array	SNP genotyping analysis	No	GRCh38.p12	NC_000015.10	15	20944756	22308242	Remapped	0.68516
nstd190	nssv16211615		deletion	1	SNP array	SNP genotyping analysis	No	GRCh38.p12	NC_000015.10	15	20944756	22308242	Remapped	0.65336
nstd190	nssv16211629		deletion	1	SNP array	SNP genotyping analysis	No	GRCh38.p12	NC_000015.10	15	20007545	22308242	Remapped	0.78989
nstd190	nssv16211630		deletion	1	SNP array	SNP genotyping analysis	No	GRCh38.p12	NC_000015.10	15	19946069	22308242	Remapped	0.79424
nstd190	nssv16211640		deletion	1	SNP array	SNP genotyping analysis	No	GRCh38.p12	NC_000015.10	15	19839089	22308242	Remapped	0.80971
nstd190	nsv4678604	copy number variation					No	GRCh38.p12	NC_000015.10	15	19839089	22308242	Remapped	0.80971
nstd190	nsv4678605	copy number variation					No	GRCh38.p12	NC_000015.10	15	19839089	22308242	Remapped	0.80138
nstd190	nsv4678606	copy number variation					No	GRCh38.p12	NC_000015.10	15	19839089	22308242	Remapped	0.798
nstd190	nsv4678607	copy number variation					No	GRCh38.p12	NC_000015.10	15	19839089	22308242	Remapped	0.79551
nstd190	nsv4678608	copy number variation					No	GRCh38.p12	NC_000015.10	15	19839089	22308242	Remapped	0.7855
nstd190	nsv4678609	copy number variation					No	GRCh38.p12	NC_000015.10	15	19839089	22308242	Remapped	0.76952
nstd190	nsv4678610	copy number variation					No	GRCh38.p12	NC_000015.10	15	19839089	26062029	Remapped	0.99363
nstd190	nsv4678611	copy number variation					No	GRCh38.p12	NC_000015.10	15	19839089	27906894	Remapped	0.99508
nstd190	nsv4678612	copy number variation					No	GRCh38.p12	NC_000015.10	15	19946069	22308242	Remapped	0.79424
nstd190	nsv4678613	copy number variation					No	GRCh38.p12	NC_000015.10	15	20007545	22308242	Remapped	0.78989
nstd190	nsv4678614	copy number variation					No	GRCh38.p12	NC_000015.10	15	20007545	22308242	Remapped	0.7791
nstd190	nsv4678615	copy number variation					No	GRCh38.p12	NC_000015.10	15	20007545	22308242	Remapped	0.75675
nstd190	nsv4678616	copy number variation					No	GRCh38.p12	NC_000015.10	15	20013263	22308242	Remapped	0.79818
nstd190	nsv4678617	copy number variation					No	GRCh38.p12	NC_000015.10	15	20013263	22308242	Remapped	0.78948
nstd190	nsv4678618	copy number variation					No	GRCh38.p12	NC_000015.10	15	20013263	22308242	Remapped	0.77867
nstd190	nsv4678619	copy number variation					No	GRCh38.p12	NC_000015.10	15	20013263	22308242	Remapped	0.75629
nstd190	nsv4678620	copy number variation					No	GRCh38.p12	NC_000015.10	15	20013263	23386710	Remapped	0.98831
nstd190	nsv4678621	copy number variation					No	GRCh38.p12	NC_000015.10	15	20028295	22308242	Remapped	0.75508
nstd190	nsv4678622	copy number variation					No	GRCh38.p12	NC_000015.10	15	20028295	23422945	Remapped	0.98838
nstd190	nsv4678623	copy number variation					No	GRCh38.p12	NC_000015.10	15	20057775	22308242	Remapped	0.75266
nstd190	nsv4678624	copy number variation					No	GRCh38.p12	NC_000015.10	15	20343543	22308242	Remapped	0.77199
nstd190	nsv4678625	copy number variation					No	GRCh38.p12	NC_000015.10	15	20343543	22308242	Remapped	0.76249
nstd190	nsv4678626	copy number variation					No	GRCh38.p12	NC_000015.10	15	20343543	22308242	Remapped	0.7445
nstd190	nsv4678627	copy number variation					No	GRCh38.p12	NC_000015.10	15	20343543	22308242	Remapped	0.72653
nstd190	nsv4678628	copy number variation					No	GRCh38.p12	NC_000015.10	15	20343543	23386710	Remapped	0.98706
nstd190	nsv4678629	copy number variation					No	GRCh38.p12	NC_000015.10	15	20343543	23415423	Remapped	0.98718
nstd190	nsv4678630	copy number variation					No	GRCh38.p12	NC_000015.10	15	20379951	22308242	Remapped	0.75909
nstd190	nsv4678631	copy number variation					No	GRCh38.p12	NC_000015.10	15	20379951	22308242	Remapped	0.72279
nstd190	nsv4678632	copy number variation					No	GRCh38.p12	NC_000015.10	15	20534837	22308242	Remapped	0.70571
nstd190	nsv4678633	copy number variation					No	GRCh38.p12	NC_000015.10	15	20861099	22308242	Remapped	0.71381
nstd190	nsv4678634	copy number variation					No	GRCh38.p12	NC_000015.10	15	20861099	22308242	Remapped	0.70282
nstd190	nsv4678635	copy number variation					No	GRCh38.p12	NC_000015.10	15	20861099	22308242	Remapped	0.69515
nstd190	nsv4678636	copy number variation					No	GRCh38.p12	NC_000015.10	15	20861099	22308242	Remapped	0.68931
nstd190	nsv4678637	copy number variation					No	GRCh38.p12	NC_000015.10	15	20861099	22308242	Remapped	0.68219
nstd190	nsv4678638	copy number variation					No	GRCh38.p12	NC_000015.10	15	20861099	22308242	Remapped	0.67162
nstd190	nsv4678639	copy number variation					No	GRCh38.p12	NC_000015.10	15	20861099	22308242	Remapped	0.66182
nstd190	nsv4678640	copy number variation					No	GRCh38.p12	NC_000015.10	15	20861099	23386710	Remapped	0.98448
nstd190	nsv4678641	copy number variation					No	GRCh38.p12	NC_000015.10	15	20944756	22308242	Remapped	0.7015
nstd190	nsv4678642	copy number variation					No	GRCh38.p12	NC_000015.10	15	20944756	22308242	Remapped	0.69586
nstd190	nsv4678643	copy number variation					No	GRCh38.p12	NC_000015.10	15	20944756	22308242	Remapped	0.69024
nstd190	nsv4678644	copy number variation					No	GRCh38.p12	NC_000015.10	15	20944756	22308242	Remapped	0.6857
nstd190	nsv4678645	copy number variation					No	GRCh38.p12	NC_000015.10	15	20944756	22308242	Remapped	0.68516
nstd190	nsv4678646	copy number variation					No	GRCh38.p12	NC_000015.10	15	20944756	22308242	Remapped	0.68238
nstd190	nsv4678647	copy number variation					No	GRCh38.p12	NC_000015.10	15	20944756	22308242	Remapped	0.67642
nstd190	nsv4678648	copy number variation					No	GRCh38.p12	NC_000015.10	15	20944756	22308242	Remapped	0.66914
nstd190	nsv4678649	copy number variation					No	GRCh38.p12	NC_000015.10	15	20944756	22308242	Remapped	0.65835
nstd190	nsv4678650	copy number variation					No	GRCh38.p12	NC_000015.10	15	20944756	22308242	Remapped	0.65485
nstd190	nsv4678651	copy number variation					No	GRCh38.p12	NC_000015.10	15	20944756	22308242	Remapped	0.65336
nstd190	nsv4678652	copy number variation					No	GRCh38.p12	NC_000015.10	15	20944756	22308242	Remapped	0.64837
nstd190	nsv4678653	copy number variation					No	GRCh38.p12	NC_000015.10	15	20944756	23653247	Remapped	0.98551

dbVar

Database of genomic structural variation

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