dbVar for Gene (Select 2348) - dbVar

loading data ...

Number of Variants: 20

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv7094183	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr11: 71,146,421-75,283,128 , GRCh38.p12 chr11: 71,435,375-75,572,083	LOC112268078, LRTOMT, 142 more genes
nsv7093946	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 71,903,218-72,019,668 , GRCh38.p12 chr11: 72,192,174-72,308,624	PHOX2A, FOLR1, 5 more genes
nsv6909791	copy number variation	1	nstd229	human		GRCh38 chr11: 72,187,701-72,193,800 , GRCh37.p13 chr11: 71,898,745-71,904,844	FOLR1
nsv6908275	copy number variation	1	nstd229	human		GRCh38 chr11: 71,281,500-72,194,614 , GRCh37.p13 chr11: 71,088,949-71,905,658	DEFB130C, ANAPC15, 40 more genes
nsv6637545	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr11: 71,777,538-72,144,933 , GRCh38.p12 chr11: 72,066,492-72,433,889	CLPB, FOLR3, 15 more genes
nsv6470560	copy number variation	1	nstd223	human		GRCh38 chr11: 72,025,209-72,302,197 , GRCh37.p13 chr11: 71,736,255-72,013,241	CLPB, FOLR3, 14 more genes
nsv6315537	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 32,799,481-134,938,470 , GRCh38.p12 chr11: 32,777,935-135,068,576	PYGM, ATL3, 2125 more genes
nsv6314007	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr11: 71,567,724-72,488,649 , GRCh38.p12 chr11: 71,856,678-72,777,604	STARD10, PDE2A, 38 more genes
nsv6309286	copy number variation	2	nstd102	human	Uncertain significance, Pathogenic	GRCh37 chr11: 71,903,218-71,903,405 , GRCh38.p12 chr11: 72,192,174-72,192,361	FOLR1
nsv5380796	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 11,835,569-118,373,112 , GRCh38.p12 chr11: 11,814,022-118,502,397	FAUP4, MMP7, 2031 more genes
nsv4987252	copy number variation	1	nstd200	human		GRCh38 chr11: 72,187,628-72,193,641 , GRCh37.p13 chr11: 71,898,672-71,904,685	FOLR1
nsv4845695	copy number variation	1	nstd200	human		GRCh37 chr11: 71,898,672-71,904,685 , GRCh38.p12 chr11: 72,187,628-72,193,641	FOLR1
nsv4681893	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr11: 71,146,401-71,907,241 , GRCh38.p12 chr11: 71,435,355-72,196,197	OR7E128P, ZNF705EP, 39 more genes
nsv4528571	copy number variation	1	nstd166	human		GRCh37.p13 chr11: 71,903,472-71,903,528 , GRCh38.p12 chr11: 72,192,428-72,192,484	FOLR1
nsv3921153	copy number variation	1	nstd102	human	Uncertain significance	GRCh38 chr11: 71,164,008-72,309,374 , GRCh37 chr11: 71,088,949-72,020,418 , NCBI36 chr11: 70,552,702-71,698,066	LOC220077, PHOX2A, 47 more genes
nsv3919985	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr11: 70,668,528-72,528,680 , GRCh37.p13 chr11: 70,990,880-72,851,032 , GRCh38.p12 chr11: 71,279,834-73,139,987	OR7E128P, OR7E87P, 68 more genes
nsv3916301	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr11: 71,928,796-77,064,521 , GRCh37 chr11: 71,639,842-76,751,808 , NCBI36 chr11: 71,317,490-76,453,216	RN7SL786P, LIPT2-AS1, 146 more genes
nsv3915804	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 71,680,927-77,943,941 , NCBI36 chr11: 71,358,575-77,621,589 , GRCh38 chr11: 71,969,881-78,232,895	TPBGL, MAP6, 173 more genes
nsv3908873	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr11: 230,616-134,938,470 , GRCh38.p12 chr11: 230,616-135,068,576	IGHMBP2, SYTL2, 2829 more genes
nsv3900144	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 198,510-134,934,063 , GRCh38.p12 chr11: 198,510-135,064,169	RTN3, KRTAP5-13P, 2833 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 83

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 83

Page of 5

Number of Variants: 20

Page of 5

Supplemental Content

Find related data

Recent activity