dbVar for Gene (Select 2670) - 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
nsv6997145	copy number variation	1	nstd229	human		GRCh38 chr17: 44,907,425-44,907,634 , GRCh37.p13 chr17: 42,984,793-42,985,002	GFAP
nsv6982861	copy number variation	1	nstd229	human		GRCh38 chr17: 38,291,672-47,498,259 , GRCh37.p13 chr17: 36,510,266-45,575,625	KRT20, PLEKHH3, 442 more genes
nsv6290455	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr17: 44,846,894-44,962,103 , GRCh37.p13 chr17: 42,924,262-43,039,471	RN7SL405P, LOC105371793, 8 more genes
nsv5554090	sequence alteration	1	nstd206	human		GRCh38 chr17: 32,109,732-67,925,723 , GRCh37.p13 chr17: 30,436,751-65,921,839	, APOH, 1099 more genes
nsv4330632	inversion	1	nstd166	human		GRCh37.p13 chr17: 18,838,526-72,042,289 , GRCh38.p12 chr17: 18,935,213-74,046,150	, ACACA, 1499 more genes
nsv4259677	copy number variation	1	nstd166	human		GRCh37.p13 chr17: 42,979,000-42,985,200 , GRCh38.p12 chr17: 44,901,632-44,907,832	FAM187A, CCDC103, 1 more genes
nsv3918486	copy number variation	1	nstd102	human	Uncertain significance	GRCh38 chr17: 44,906,235-45,220,406 , NCBI36 chr17: 40,339,129-40,653,556 , GRCh37 chr17: 42,983,603-43,297,773	GFAP, MIR6783, 16 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
nsv3913552	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr17: 36,449,220-75,053,130 , NCBI36 chr17: 54,950,518-70,560,820 , GRCh37 chr17: 57,595,736-73,049,225	RNU6-131P, ZNF652, 1075 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
nsv3911563	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr17: 45,918,236-63,677,950 , GRCh37 chr17: 48,563,237-65,936,105 , GRCh38 chr17: 36,449,220-68,170,214	PLEKHH3, CHCT1, 958 more genes
nsv3911344	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 37,356,126-43,706,945 , NCBI36 chr17: 34,609,652-41,062,728 , GRCh38 chr17: 39,199,873-45,629,579	IFI35, RND2, 345 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
nsv3907100	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 42,969,980-42,993,118 , GRCh38.p12 chr17: 44,892,612-44,915,750	EFTUD2, CCDC103, 2 more genes
nsv3906245	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 12,344-81,057,996 , GRCh38.p12 chr17: 162,553-83,100,251	MIR21, LOC105371899, 2366 more genes
nsv3903684	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 8,547-81,060,040 , GRCh38.p12 chr17: 158,756-83,102,004	MIR3185, YWHAEP6, 2366 more genes
nsv3899740	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 7,214-81,058,310 , GRCh38.p12 chr17: 157,423-83,100,564	P4HB, LOC105371808, 2366 more genes
nsv3899474	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr17: 42,649,083-43,659,985 , GRCh38.p12 chr17: 44,571,715-45,582,619	PLEKHM1, HIGD1B, 45 more genes
nsv3158725	copy number variation	1	nstd151	human		GRCh37 chr17: 42,979,684-42,984,761 , GRCh38.p12 chr17: 44,902,316-44,907,393	FAM187A, GFAP, 1 more genes

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Number of Variants: 20

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