dbVar for Gene (Select 406906) - dbVar

loading data ...

Number of Variants: 20

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv6112815	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr18: 54,285,235-77,960,815 , GRCh38.p12 chr18: 56,618,004-80,202,932	RPL31P9, TRG-TCC5-1, 271 more genes
nsv6112802	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr18: 23,626,739-78,014,976 , GRCh38.p12 chr18: 26,046,775-80,257,093	RPL9P31, LINC02582, 595 more genes
nsv5381802	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr18: 51,925,586-78,010,032 , GRCh38.p12 chr18: 54,399,216-80,252,149	LOC105372200, LOC105372174, 298 more genes
nsv5381190	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr18: 55,225,777-56,940,458 , GRCh38.p12 chr18: 57,558,545-59,273,226	TRG-TCC6-1, RAX, 32 more genes
nsv5018289	copy number variation	1	nstd200	human		GRCh38 chr18: 58,448,096-58,451,044 , GRCh37.p13 chr18: 56,115,328-56,118,276	MIR3591, MIR122
nsv4676158	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr18: 55,458,425-78,014,123 , GRCh38.p12 chr18: 57,791,193-80,256,240	LOC105372140, LOC105372143, 253 more genes
nsv4676105	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr18: 49,460,596-78,014,123 , GRCh38.p12 chr18: 51,934,226-80,256,240	MIR548AV, GTSCR1, 310 more genes
nsv4457866	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr18: 45,621,155-61,416,536 , GRCh38.p12 chr18: 48,094,784-63,749,302	LOC105372159, LOC105372156, 208 more genes
nsv4457768	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr18: 55,991,937-56,852,926 , GRCh38.p12 chr18: 58,324,705-59,185,694	NEDD4L, LOC100286992, 17 more genes
nsv4457536	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr18: 56,018,446-56,116,713 , GRCh38.p12 chr18: 58,351,214-58,449,481	NEDD4L, MIR122, 1 more genes
nsv4457436	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr18: 56,018,446-56,119,213 , GRCh38.p12 chr18: 58,351,214-58,451,981	MIR3591, NEDD4L, 1 more genes
nsv4453843	copy number variation	1	nstd102	human	Uncertain significance	GRCh38 chr18: 57,558,545-59,273,226 , GRCh37 chr18: 55,225,777-56,940,458	TRG-TCC5-1, RAX, 32 more genes
nsv4415942	copy number variation	1	nstd174	human		GRCh37 chr18: 56,017,523-56,119,629 , GRCh38.p12 chr18: 58,350,291-58,452,397	, NEDD4L, 2 more genes
nsv4336672	sequence alteration	1	nstd166	human		GRCh37.p13 chr18: 21,176,191-70,772,863 , GRCh38.p12 chr18: 23,596,227-73,105,628	, CDH2, 557 more genes
nsv4320417	inversion	1	nstd166	human		GRCh37.p13 chr18: 52,530,154-56,173,673 , GRCh38.p12 chr18: 54,862,923-58,506,441	, ONECUT2, 50 more genes
nsv3924706	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr18: 136,227-78,014,123 , GRCh38 chr18: 136,227-80,256,240 , NCBI36 chr18: 126,227-76,115,097	LOC100420948, NPM1P2, 941 more genes
nsv3924638	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr18: 20,962,119-74,691,446 , NCBI36 chr18: 16,796,078-70,532,390 , GRCh37 chr18: 18,542,080-72,403,402	HMGN1P30, LOC107985134, 596 more genes
nsv3924351	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr18: 108,760-76,113,817 , GRCh38 chr18: 118,760-80,254,946 , GRCh37 chr18: 118,760-78,012,829	MIX23P1, LOC105372087, 942 more genes
nsv3923854	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr18: 50,675,985-56,408,844 , GRCh38 chr18: 54,857,756-60,590,631 , GRCh37 chr18: 52,524,987-58,257,864	ZNF532, LOC105372155, 90 more genes
nsv3923838	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr18: 138,963-76,103,255 , GRCh37 chr18: 148,963-78,002,264 , GRCh38 chr18: 148,963-80,244,381	WDR7-OT1, HMGN1P30, 941 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 200

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 200

Page of 10

Number of Variants: 20

Page of 10

Supplemental Content

Find related data

Recent activity