dbVar for Gene (Select 2956) - 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
nsv6137677	copy number variation	1	nstd102	human	not provided	GRCh38 chr2: 47,804,639-48,361,567 , GRCh37.p13 chr2: 48,031,778-48,588,706	RNU4-49P, RN7SKP224, 11 more genes
nsv5673706	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 47,635,530-48,035,526 , GRCh38.p12 chr2: 47,408,391-47,808,387	MSH6, MSH2, 7 more genes
nsv5673624	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 48,030,537-48,032,176 , GRCh38.p12 chr2: 47,803,398-47,805,037	MSH6, FBXO11
nsv5673623	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 48,023,023-48,033,800 , GRCh38.p12 chr2: 47,795,884-47,806,661	RPL36AP15, MSH6, 1 more genes
nsv5673622	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 48,023,023-48,028,304 , GRCh38.p12 chr2: 47,795,884-47,801,165	MSH6, RPL36AP15
nsv5673548	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 48,010,211-48,033,885 , GRCh38.p12 chr2: 47,783,072-47,806,746	MSH6, FBXO11, 1 more genes
nsv5673463	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 48,025,740-48,032,937 , GRCh38.p12 chr2: 47,798,601-47,805,798	FBXO11, MSH6, 1 more genes
nsv5673462	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 48,025,740-48,032,572 , GRCh38.p12 chr2: 47,798,601-47,805,433	FBXO11, MSH6, 1 more genes
nsv5673461	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 48,023,027-48,032,172 , GRCh38.p12 chr2: 47,795,888-47,805,033	FBXO11, RPL36AP15, 1 more genes
nsv5673460	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 48,018,060-48,033,503 , GRCh38.p12 chr2: 47,790,921-47,806,364	FBXO11, RPL36AP15, 1 more genes
nsv5673368	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr2: 48,033,306-48,033,380 , GRCh38 chr2: 47,806,167-47,806,241	MSH6, FBXO11
nsv5564424	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr2: 47,806,200-47,806,639 , GRCh37 chr2: 48,033,339-48,033,778	MSH6, FBXO11
nsv5564335	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 48,032,047-48,032,167 , GRCh38 chr2: 47,804,908-47,805,028	MSH6, FBXO11
nsv5564334	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 48,010,371-48,014,019 , GRCh38 chr2: 47,783,232-47,786,880	MSH6
nsv5564249	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr2: 47,783,232-47,787,317 , GRCh37 chr2: 48,010,371-48,014,456	MSH6
nsv5564182	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr2: 47,795,892-47,796,064 , GRCh37 chr2: 48,023,031-48,023,203	RPL36AP15, MSH6
nsv5554214	mobile element insertion	1	nstd206	human		GRCh38 chr2: 43,826,578-177,947,868 , GRCh37.p13 chr2: 44,053,717-178,812,595	, POLR1B, 2149 more genes
nsv5439171	copy number variation	1	nstd206	human		GRCh38 chr2: 46,970,724-48,057,041 , GRCh37.p13 chr2: 47,197,863-48,284,180	, LOC105374589, 24 more genes
nsv5437867	copy number variation	1	nstd206	human		GRCh38 chr2: 47,804,054-47,804,319 , GRCh37.p13 chr2: 48,031,193-48,031,458	MSH6
nsv5381582	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr2: 47,672,677-51,259,192 , GRCh38.p12 chr2: 47,445,538-51,032,054	RPL18AP6, RNU6-282P, 39 more genes

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Number of Variants: 20

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Items: 1 to 20 of 261

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Number of Variants: 20

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