dbVar for Gene (Select 15) - 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
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
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
nsv4859029	copy number variation	1	nstd200	human		GRCh37 chr17: 74,461,486-74,461,979 , GRCh38.p12 chr17: 76,465,404-76,465,897	AANAT
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
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
nsv4631437	copy number variation	1	nstd183	human		GRCh37 chr17: 74,455,272-74,476,980 , GRCh38.p12 chr17: 76,459,190-76,480,898	AANAT, RHBDF2
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
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
nsv4339471	sequence alteration	1	nstd166	human		GRCh37.p13 chr17: 74,454,070-74,479,461 , GRCh38.p12 chr17: 76,457,988-76,483,379	AANAT, RHBDF2
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
nsv4270345	copy number variation	1	nstd166	human		GRCh37.p13 chr17: 74,455,034-74,471,079 , GRCh38.p12 chr17: 76,458,952-76,474,997	AANAT, RHBDF2
nsv4254358	copy number variation	1	nstd166	human		GRCh37.p13 chr17: 74,456,327-75,011,803 , GRCh38.p12 chr17: 76,460,245-77,015,721	RNU6-97P, RHBDF2, 24 more genes
nsv3972399	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr17: 64,159,738-74,891,024 , GRCh38.p12 chr17: 66,163,620-76,894,942	AANAT, ACOX1, 243 more genes
nsv3919156	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr17: 69,916,435-83,102,552 , GRCh37 chr17: 67,912,576-81,048,189 , NCBI36 chr17: 65,424,171-78,653,717	CD300A, RNF213, 359 more genes
nsv3917654	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr17: 64,716,815-78,637,842 , GRCh37 chr17: 67,205,220-81,044,553 , GRCh38 chr17: 69,209,079-83,086,677	LOC101928447, GRB2, 368 more genes
nsv3914783	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr17: 16,698,288-78,654,742 , GRCh37.p13 chr17: 16,757,563-81,048,189 , GRCh38.p12 chr17: 16,854,249-83,103,577	LOC105371922, GJD3, 1855 more genes
nsv3911811	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr17: 31,824,931-78,654,742 , GRCh37.p13 chr17: 34,750,818-81,048,189 , GRCh38.p12 chr17: 36,382,248-83,103,577	PRPSAP1, CACNG1, 1350 more genes
nsv3909523	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 63,689,671-81,041,938 , GRCh38.p12 chr17: 65,693,553-83,084,062	RPL38, RNF157-AS1, 428 more genes
nsv3909511	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 42,580,684-81,085,615 , GRCh38.p12 chr17: 44,503,316-83,137,846	FOXK2, SOCS3-DT, 958 more genes
nsv3907261	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr17: 526-81,041,938 , GRCh38.p12 chr17: 150,733-83,084,062	SMURF2, LOC112268199, 2366 more genes

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Has Clinical Interpretation

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Items: 1 to 20 of 167

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Number of Variants: 20

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