dbVar for Gene (Select 113218490) - dbVar

loading data ...

Number of Variants: 20

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv5381771	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 22,149-29,048,823 , GRCh38.p12 chr5: 22,149-29,048,716	OTULINL, AKTIPP2, 317 more genes
nsv4729109	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr5: 16,741,484-23,963,898 , GRCh38.p12 chr5: 16,741,375-23,963,789	LOC105374672, LOC105374669, 70 more genes
nsv4685752	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 71,904-22,078,969 , GRCh38.p12 chr5: 71,789-22,078,860	LINC01377, LOC100421308, 277 more genes
nsv4674161	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 113,576-23,364,376 , GRCh38.p12 chr5: 113,461-23,364,267	LOC102723561, LOC107986397, 287 more genes
nsv4456248	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr5: 11,182,916-18,624,750 , GRCh38.p12 chr5: 11,182,804-18,624,641	OTULIN, LINC02218, 83 more genes
nsv4436202	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr5: 14,685,137-149,511,942 , GRCh38.p12 chr5: 14,685,028-150,132,379	RNU1-150P, RNU6-727P, 1757 more genes
nsv4349271	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 140,474-26,906,925 , GRCh38.p12 chr5: 140,359-26,906,816	MIR4636, LRRC14B, 304 more genes
nsv4127144	copy number variation	1	nstd166	human		GRCh37.p13 chr5: 17,155,517-17,158,669 , GRCh38.p12 chr5: 17,155,408-17,158,560	BASP1-AS1, RNA5SP180, 1 more genes
nsv3924736	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr5: 75,149-33,454,051 , GRCh38 chr5: 22,149-33,418,188 , GRCh37 chr5: 22,149-33,418,294	LOC105374678, ZFR, 369 more genes
nsv3924496	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 22,149-32,248,116 , NCBI36 chr5: 75,149-32,283,873 , GRCh38 chr5: 22,149-32,248,010	LOC105374678, MIR4278, 356 more genes
nsv3924040	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr5: 16,877,035-19,512,469 , GRCh37.p13 chr5: 16,824,035-19,476,712 , GRCh38.p12 chr5: 16,823,926-19,476,603	RNA5SP179, RPS26P28, 40 more genes
nsv3923992	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 50,093-46,115,086 , NCBI36 chr5: 103,093-46,150,843 , GRCh38 chr5: 49,978-46,114,984	LOC100130748, CDH10, 533 more genes
nsv3923396	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 22,149-27,188,057 , NCBI36 chr5: 75,149-27,223,814 , GRCh38 chr5: 22,149-27,187,950	LINC02899, TERLR1, 307 more genes
nsv3922865	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr5: 22,149-28,429,241 , GRCh37 chr5: 22,149-28,429,348 , NCBI36 chr5: 75,149-28,465,105	CCT6P2, LOC105374661, 312 more genes
nsv3922816	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr5: 75,149-26,629,757 , GRCh38 chr5: 22,149-26,593,891 , GRCh37 chr5: 22,149-26,594,000	SPICP4, RNU6-679P, 304 more genes
nsv3922539	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr5: 107,954-35,716,704 , GRCh37 chr5: 54,954-35,680,947 , GRCh38 chr5: 54,839-35,680,845	MTCYBP37, LINC01020, 398 more genes
nsv3921039	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr5: 22,149-23,607,053 , GRCh37 chr5: 22,149-23,607,162 , NCBI36 chr5: 75,149-23,642,919	LOC391768, RNA5SP178, 290 more genes
nsv3920848	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr5: 75,149-23,167,912 , GRCh37 chr5: 22,149-23,132,155 , GRCh38 chr5: 22,149-23,132,046	RETREG1-AS1, LOC105374657, 285 more genes
nsv3918815	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 22,149-25,699,714 , GRCh38 chr5: 22,149-25,699,605 , NCBI36 chr5: 75,149-25,735,471	TAF11L4, TERT, 302 more genes
nsv3918728	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr5: 4,849,498-36,818,719 , NCBI36 chr5: 4,902,611-36,854,578 , GRCh37 chr5: 4,849,611-36,818,821	LINC02100, FTH1P10, 334 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 156

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 156

Page of 8

Number of Variants: 20

Page of 8

Supplemental Content

Find related data

Recent activity