"nstd72"[study] AND "deletion"[variant_type] - dbVar

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Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Location	Genes in region
nsv949748	copy number variation	1	nstd72	human	GRCh37 chrX: 1,331,659-1,655,360 , GRCh38.p12 chrX: 1,212,766-1,536,467	SLC25A6, CSF2RA, 13 more genes
nsv949751	copy number variation	1	nstd72	human	GRCh37 chrX: 1,331,650-1,654,735 , GRCh38.p12 chrX: 1,212,757-1,535,842	SLC25A6, CSF2RA, 13 more genes
nsv949750	copy number variation	1	nstd72	human	GRCh37 chrX: 1,333,752-1,655,498 , GRCh38.p12 chrX: 1,214,859-1,536,605	SLC25A6, CSF2RA, 12 more genes
nsv949749	copy number variation	1	nstd72	human	GRCh37 chrX: 1,333,753-1,655,364 , GRCh38.p12 chrX: 1,214,860-1,536,471	SLC25A6, CSF2RA, 12 more genes
nsv949747	copy number variation	1	nstd72	human	GRCh37 chrX: 1,333,547-1,654,735 , GRCh38.p12 chrX: 1,214,654-1,535,842	SLC25A6, CSF2RA, 12 more genes