dbVar for Gene (Select 100422978) - dbVar

loading data ...

Number of Variants: 20

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv7066785	inversion	1	nstd229	human		GRCh38 chr17: 48,650,784-48,769,648 , GRCh37.p13 chr17: 46,728,146-46,847,010	TTLL6, LOC105371812, 9 more genes
nsv6637543	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr17: 46,753,824-47,577,721 , GRCh38.p12 chr17: 48,676,462-49,500,359	CALCOCO2, SUMO2P17, 37 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
nsv5026313	copy number variation	1	nstd200	human		GRCh38 chr17: 48,721,867-48,751,113 , GRCh37.p13 chr17: 46,799,229-46,828,475	HOXB13, PRAC1, 4 more genes
nsv5013785	copy number variation	1	nstd200	human		GRCh38 chr17: 48,719,127-49,313,149 , GRCh37.p13 chr17: 46,796,489-47,390,511	, UBE2Z, 30 more genes
nsv5013784	copy number variation	1	nstd200	human		GRCh38 chr17: 48,704,646-48,922,409 , GRCh37.p13 chr17: 46,782,008-46,999,771	SUMO2P17, HOXB13, 15 more genes
nsv4867211	copy number variation	1	nstd200	human		GRCh37 chr17: 46,799,229-46,828,475 , GRCh38.p12 chr17: 48,721,867-48,751,113	HOXB13, PRAC1, 4 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
nsv3920056	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr17: 43,882,989-44,985,282 , GRCh38 chr17: 48,450,628-49,552,921 , GRCh37 chr17: 46,527,990-47,630,283	ZNF652-AS1, RPS10P25, 55 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
nsv3913486	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr17: 48,520,885-49,511,208 , NCBI36 chr17: 43,953,246-44,943,569 , GRCh37 chr17: 46,598,247-47,588,570	MIR6165, NGFR, 54 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
nsv3911757	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr17: 43,419,251-44,761,758 , GRCh37 chr17: 46,064,252-47,406,759 , GRCh38 chr17: 47,986,886-49,329,397	LINC02086, RNU6-1152P, 59 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
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
nsv3901021	copy number variation	1	nstd102	human	Benign	GRCh37 chr17: 46,788,433-46,977,125 , GRCh38.p12 chr17: 48,711,071-48,899,763	SUMO2P17, ATP5MC1, 13 more genes

dbVar

Result Filters

Object Type

Organism

Variant Type

Method Type

Clinical Interpretation

Has Clinical Interpretation

Sex of Subject

Origin

Study Type

Subject Phenotype Status

Additional filters

Send to:

Links from Gene

Items: 1 to 20 of 131

Number of Variants: 20

Send to:

Supplemental Content

Find related data

Recent activity

dbVar

Result Filters

Object Type

Organism

Variant Type

Method Type

Clinical Interpretation

Has Clinical Interpretation

Sex of Subject

Origin

Study Type

Subject Phenotype Status

Additional filters

Links from Gene

Items: 1 to 20 of 131

Page of 7

Number of Variants: 20

Page of 7

Supplemental Content

Find related data

Recent activity