dbVar for Gene (Select 25845) - dbVar

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Number of Variants: 20

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv6112732	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 13,200-4,012,072 , GRCh38.p12 chr5: 13,200-4,011,958	SLC9A3-AS1, LOC107984098, 76 more genes
nsv5968719	inversion	1	nstd209	human		GRCh38 chr5: 239,340-1,590,367 , GRCh37.p13 chr5: 239,455-1,590,482	, SDHA, 43 more genes
nsv5956528	insertion	1	nstd209	human		GRCh37.p13 chr5: 473,259-473,259 , GRCh38 chr5: 473,144-473,144	SLC9A3, SLC9A3-OT1, 1 more genes
nsv5843009	copy number variation	1	nstd209	human		GRCh38 chr5: 472,629-475,122 , GRCh37.p13 chr5: 472,744-475,237	SLC9A3, SLC9A3-OT1, 1 more genes
nsv5843007	copy number variation	1	nstd209	human		GRCh38 chr5: 468,339-486,789 , GRCh37.p13 chr5: 468,454-486,904	SLC9A3, SLC9A3-OT1, 1 more genes
nsv5634018	insertion	1	nstd207	human		GRCh38 chr5: 473,144-473,144 , GRCh37.p13 chr5: 473,259-473,259	SLC9A3, SLC9A3-OT1, 1 more genes
nsv5460235	copy number variation	1	nstd206	human		GRCh38 chr5: 365,337-589,487 , GRCh37.p13 chr5: 365,452-589,602	LOC107986395, EXOC3-AS1, 10 more genes
nsv5381771	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 22,149-29,048,823 , GRCh38.p12 chr5: 22,149-29,048,716	OTULINL, AKTIPP2, 317 more genes
nsv4944250	copy number variation	1	nstd200	human		GRCh38 chr5: 454,264-691,959 , GRCh37.p13 chr5: 454,379-692,074	EXOC3, SLC9A3-AS1, 11 more genes
nsv4944243	copy number variation	1	nstd200	human		GRCh38 chr5: 355,850-669,050 , GRCh37.p13 chr5: 355,965-669,165	SLC9A3-AS1, MIR4456, 14 more genes
nsv4944242	copy number variation	1	nstd200	human		GRCh38 chr5: 351,461-809,069 , GRCh37.p13 chr5: 351,576-809,184	, LOC107986395, 18 more genes
nsv4944240	copy number variation	1	nstd200	human		GRCh38 chr5: 336,679-540,584 , GRCh37.p13 chr5: 336,794-540,699	SLC9A3-OT1, LOC100310782, 8 more genes
nsv4936700	copy number variation	1	nstd200	human		GRCh38 chr5: 322,110-525,515 , GRCh37.p13 chr5: 322,225-525,630	SLC9A3, EXOC3, 7 more genes
nsv4794816	copy number variation	1	nstd200	human		GRCh37 chr5: 454,379-692,074 , GRCh38.p12 chr5\|NT_187550.1: 1-126,137 , GRCh38.p12 chr5: 454,264-691,959	LOC105374608, SLC9A3-OT1, 11 more genes
nsv4729427	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr5: 113,576-1,286,005 , GRCh38.p12 chr5: 113,461-1,285,890	SLC6A18, ZDHHC11B, 36 more genes
nsv4728897	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 113,576-4,305,172 , GRCh38.p12 chr5: 113,461-4,305,059	PPP4R2P1, MIR6075, 75 more genes
nsv4685752	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 71,904-22,078,969 , GRCh38.p12 chr5: 71,789-22,078,860	LINC01377, LOC100421308, 277 more genes
nsv4682703	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 218,461-1,295,161 , GRCh38.p12 chr5: 218,346-1,295,046	PPP4R2P1, SLC9A3-AS1, 34 more genes
nsv4682286	copy number variation	2	nstd102	human	Pathogenic, Uncertain significance	GRCh37 chr5: 218,464-1,297,488 , GRCh38.p12 chr5: 218,349-1,297,373	ZDHHC11B, LOC107986395, 34 more genes
nsv4674705	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 113,576-5,657,333 , GRCh38.p12 chr5: 113,461-5,657,220	LOC101929898, MIR4635, 90 more genes

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Items: 1 to 20 of 667

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Number of Variants: 20

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