"nstd125"[study] AND "copy number loss"[variant_type] - dbVar

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Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Location	Genes in region
nsv2768222	copy number variation	1	nstd125	human	GRCh37 chr5: 88,921,368-88,960,399 , GRCh38.p12 chr5: 89,625,551-89,664,582	LINC02161
nsv2768224	copy number variation	1	nstd125	human	GRCh37 chr6: 66,019,907-70,983,742 , GRCh38.p12 chr6: 65,310,014-70,274,039	ADGRB3, COL9A1, 29 more genes
nsv2768227	copy number variation	1	nstd125	human	GRCh37 chr9: 93,173,989-96,115,678 , GRCh38.p12 chr9: 90,411,707-93,353,396	AUH, ECM2, 68 more genes
nsv2768201	copy number variation	3	nstd125	human	GRCh37 chr2: 111,388,618-113,111,856 , GRCh38.p12 chr2: 110,631,041-112,354,279	BUB1, BCL2L11, 31 more genes
nsv2768226	copy number variation	1	nstd125	human	GRCh37 chr7: 45,373,134-47,029,521 , GRCh38.p12 chr7: 45,333,535-46,989,923	ADCY1, IGFBP1, 24 more genes