dbVar for Gene (Select 55588) - dbVar

loading data ...

Number of Variants: 20

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv5944000	copy number variation	1	nstd209	human		GRCh38 chr19: 39,387,653-39,412,021 , GRCh37.p13 chr19: 39,878,293-39,902,661	ZFP36, PAF1, 5 more genes
nsv5939047	copy number variation	1	nstd209	human		GRCh38 chr19: 39,396,176-39,396,759 , GRCh37.p13 chr19: 39,886,816-39,887,399	MED29
nsv5873243	copy number variation	1	nstd209	human		GRCh38 chr19: 39,390,235-39,395,534 , GRCh37.p13 chr19: 39,880,875-39,886,174	MED29, PAF1, 1 more genes
nsv5533340	copy number variation	1	nstd206	human		GRCh38 chr19: 39,393,240-39,394,775 , GRCh37.p13 chr19: 39,883,880-39,885,415	MED29
nsv5516334	copy number variation	1	nstd206	human		GRCh38 chr19: 39,396,176-39,396,760 , GRCh37.p13 chr19: 39,886,816-39,887,400	MED29
nsv5287708	copy number variation	1	nstd204	human		GRCh38.p13 chr19: 39,400,928-39,404,176 , GRCh37.p13 chr19: 39,891,568-39,894,816	MED29
nsv5167680	mobile element insertion	1	nstd203	human		GRCh38 chr19: 39,399,852-39,399,868 , GRCh37.p13 chr19: 39,890,492-39,890,508	MED29
nsv5027943	copy number variation	1	nstd200	human		GRCh38 chr19: 39,393,285-39,395,015 , GRCh37.p13 chr19: 39,883,925-39,885,655	MED29
nsv4868335	copy number variation	1	nstd200	human		GRCh37 chr19: 39,886,838-39,887,389 , GRCh38.p12 chr19: 39,396,198-39,396,749	MED29
nsv4868334	copy number variation	1	nstd200	human		GRCh37 chr19: 39,883,920-39,885,655 , GRCh38.p12 chr19: 39,393,280-39,395,015	MED29
nsv4628819	copy number variation	1	nstd183	human		GRCh37 chr19: 39,811,570-39,886,212 , GRCh38.p12 chr19: 39,320,930-39,395,572	GMFG, PAF1, 4 more genes
nsv4624865	copy number variation	1	nstd183	human		GRCh37 chr19: 39,881,236-39,904,463 , GRCh38.p12 chr19: 39,390,596-39,413,823	ZFP36, PAF1, 5 more genes
nsv4457372	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr19: 28,271,106-49,213,832 , GRCh38.p12 chr19: 27,780,198-48,710,575	ZNF461, LOC101927572, 735 more genes
nsv4257513	copy number variation	1	nstd166	human		GRCh37.p13 chr19: 39,886,854-39,887,387 , GRCh38.p12 chr19: 39,396,214-39,396,747	MED29
nsv3913730	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr19: 11,199,618-49,821,491 , GRCh37 chr19: 11,338,618-45,129,651 , GRCh38 chr19: 11,227,942-44,626,354	BCKDHA, ADGRE5, 1102 more genes
nsv3912447	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr19: 42,502,119-47,934,680 , GRCh37 chr19: 37,810,279-43,242,840 , GRCh38 chr19: 37,319,377-42,738,688	MIR8077, TRI-TAT1-1, 233 more genes
nsv3904885	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr19: 68,029-59,110,290 , GRCh38.p12 chr19: 68,029-58,598,923	ZNF321P, ZNF861P, 2443 more genes
nsv3903203	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr19: 260,912-59,097,160 , GRCh38.p12 chr19: 260,912-58,585,793	BABAM1, BEST2, 2426 more genes
nsv3903092	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr19: 260,912-58,956,888 , GRCh38.p12 chr19: 260,912-58,445,521	LENG8, SYDE1, 2408 more genes
nsv3895066	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr19: 37,582,250-41,630,908 , GRCh38.p12 chr19: 37,091,348-41,125,003	RNU6-140P, COQ8B, 162 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 159

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 159

Page of 8

Number of Variants: 20

Page of 8

Supplemental Content

Find related data

Recent activity