dbVar for Gene (Select 9110) - 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
nsv5942591	copy number variation	1	nstd209	human		GRCh38 chr17: 58,488,483-58,488,735 , GRCh37.p13 chr17: 56,565,844-56,566,096	MTMR4, HSF5
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
nsv5381036	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr17: 56,432,304-56,811,583 , GRCh38.p12 chr17: 58,354,943-58,734,222	SEPTIN4-AS1, MTMR4, 13 more genes
nsv4851469	copy number variation	1	nstd200	human		GRCh37 chr17: 56,593,730-56,594,107 , GRCh38.p12 chr17: 58,516,369-58,516,746	MTMR4
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
nsv4262710	copy number variation	1	nstd166	human		GRCh37.p13 chr17: 56,591,250-56,597,500 , GRCh38.p12 chr17: 58,513,889-58,520,139	SEPTIN4, SEPTIN4-AS1, 1 more genes
nsv3914957	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 55,496,167-57,812,825 , GRCh38 chr17: 57,418,806-59,735,464 , NCBI36 chr17: 52,851,166-55,167,607	CLTC, LOC101927557, 67 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
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
nsv3906711	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr17: 55,916,829-56,770,618 , GRCh38.p12 chr17: 57,839,468-58,693,257	LPO, MPO, 34 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
nsv3895703	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 56,321,134-62,080,001 , GRCh38.p12 chr17: 58,243,773-64,002,641	GH2, LOC105371847, 161 more genes
nsv3892374	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 52,189,051-57,477,162 , GRCh38.p12 chr17: 54,111,690-59,399,801	RN7SKP14, RNU6-1249P, 93 more genes
nsv3890268	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 49,076,980-58,740,945 , GRCh38.p12 chr17: 50,999,619-60,663,584	NDUFB8P2, LPO, 161 more genes

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Number of Variants: 20

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