dbVar for Gene (Select 768206) - 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
nsv5946294	copy number variation	1	nstd209	human		GRCh38 chr17: 76,525,968-76,526,269 , GRCh37.p13 chr17: 74,522,050-74,522,351	PRCD, CYGB
nsv5655388	insertion	1	nstd207	human		GRCh38 chr17: 76,527,197-76,527,197 , GRCh37.p13 chr17: 74,523,279-74,523,279	CYGB, PRCD
nsv5655113	insertion	1	nstd207	human		GRCh38 chr17: 76,527,076-76,527,076 , GRCh37.p13 chr17: 74,523,158-74,523,158	PRCD, CYGB
nsv5651268	insertion	1	nstd207	human		GRCh38 chr17: 76,526,839-76,526,839 , GRCh37.p13 chr17: 74,522,921-74,522,921	CYGB, PRCD
nsv5650236	insertion	1	nstd207	human		GRCh38 chr17: 76,526,912-76,526,912 , GRCh37.p13 chr17: 74,522,994-74,522,994	PRCD, CYGB
nsv5603199	copy number variation	1	nstd207	human		GRCh38 chr17: 76,525,968-76,526,269 , GRCh37.p13 chr17: 74,522,050-74,522,351	PRCD, CYGB
nsv5525355	copy number variation	1	nstd206	human		GRCh38 chr17: 76,550,542-76,584,098 , GRCh37.p13 chr17: 74,546,624-74,580,180	ST6GALNAC2, CYGB, 5 more genes
nsv5524662	copy number variation	1	nstd206	human		GRCh38 chr17: 76,540,688-76,540,782 , GRCh37.p13 chr17: 74,536,770-74,536,864	CYGB, PRCD
nsv5523731	copy number variation	1	nstd206	human		GRCh38 chr17: 76,530,950-76,531,013 , GRCh37.p13 chr17: 74,527,032-74,527,095	PRCD, CYGB
nsv5293343	copy number variation	1	nstd204	human		GRCh38.p13 chr17: 74,899,101-76,684,700 , GRCh37.p13 chr17: 72,895,199-74,680,782	, RNU6-24P, 92 more genes
nsv5155399	mobile element insertion	1	nstd203	human		GRCh38 chr17: 76,550,120-76,550,135 , GRCh37.p13 chr17: 74,546,202-74,546,217	PRCD, CYGB
nsv5014037	copy number variation	1	nstd200	human		GRCh38 chr17: 76,464,936-76,534,469 , GRCh37.p13 chr17: 74,461,018-74,530,551	RHBDF2, AANAT, 2 more genes
nsv4758010	insertion	1	nstd199	human		GRCh37 chr17: 74,522,856-74,522,856 , GRCh38.p12 chr17: 76,526,774-76,526,774	CYGB, PRCD
nsv4680180	copy number variation	1	nstd189	human		GRCh37.p13 chr17: 74,053,616-74,648,486 , GRCh38.p12 chr17: 76,057,535-76,652,404	, AANAT, 30 more genes
nsv4676341	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr17: 74,509,193-75,602,123 , GRCh38.p12 chr17: 76,513,111-77,606,041	CYCSP40, RNU6-97P, 38 more genes
nsv4676104	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 73,261,871-78,608,763 , GRCh38.p12 chr17: 75,265,790-80,634,963	LLGL2, TSEN54, 165 more genes
nsv4457881	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr17: 74,401,337-74,574,103 , GRCh38.p12 chr17: 76,405,256-76,578,021	SNHG16, PRCD, 9 more genes
nsv4457860	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr17: 74,523,892-74,574,103 , GRCh38.p12 chr17: 76,527,810-76,578,021	CYGB, SNHG16, 5 more genes
nsv4457646	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 62,778,720-81,041,938 , GRCh38.p12 chr17: 64,782,602-83,084,062	LOC107985089, ARSG, 448 more genes
nsv4272382	copy number variation	1	nstd166	human		GRCh37.p13 chr17: 74,461,132-74,530,513 , GRCh38.p12 chr17: 76,465,050-76,534,431	CYGB, PRCD, 2 more genes

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Number of Variants: 20

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Has Clinical Interpretation

Sex of Subject

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Items: 1 to 20 of 205

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Number of Variants: 20

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