dbVar data for all organisms

Variant Placements (including Supporting Variants) for nstd139
Study ID	Variant ID	Variant Region type	Variant Call type	Method	Analysis ID	Validation	Variant samples	Subject phenotype	Assembly	Accession	Chr	Start	End	Placement Type	Remap Score
nstd139	nssv14038721		copy number loss	Sequencing	Paired-end mapping	No	6209342	Male infertility	GRCh37 (hg19)	NC_000015.9	15	43894500	43950000	Submitted genomic
nstd139	nssv14038721		copy number loss	Sequencing	Paired-end mapping	No	6209342	Male infertility	GRCh37 (hg19)	NC_000015.9	15	43894500	43950000	Submitted genomic
nstd139	nssv14038721		copy number loss	Sequencing	Paired-end mapping	No	6209342	Male infertility	GRCh38.p12	NC_000015.10	15	43602302	43657802	Remapped	1
nstd139	nsv3067119	copy number variation				No			GRCh37 (hg19)	NC_000015.9	15	43894500	43950000	Submitted genomic
nstd139	nsv3067119	copy number variation				No			GRCh37 (hg19)	NC_000015.9	15	43894500	43950000	Submitted genomic
nstd139	nsv3067119	copy number variation				No			GRCh38.p12	NC_000015.10	15	43602302	43657802	Remapped	1

dbVar