slc6a5[All Fields] AND 1[has_clinical] - dbVar

loading data ...

Number of Variants: 20

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv6309045	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 20,621,219-20,668,500 , GRCh38.p12 chr11: 20,599,673-20,646,954	SLC6A5
nsv7093679	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 20,612,464-20,622,873 , GRCh38.p12 chr11: 20,590,918-20,601,327	SLC6A5
nsv6308969	copy number variation	2	nstd102	human	Pathogenic, Likely pathogenic	GRCh37 chr11: 20,668,360-20,668,500 , GRCh38.p12 chr11: 20,646,814-20,646,954	SLC6A5
nsv7098804	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr11: 20,649,564-20,658,277 , GRCh38 chr11: 20,628,018-20,636,731	SLC6A5
nsv6309186	copy number variation	2	nstd102	human	Uncertain significance	GRCh37 chr11: 20,673,815-20,676,414 , GRCh38.p12 chr11: 20,652,269-20,654,868	SLC6A5
nsv7093842	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr11: 20,648,234-20,676,414 , GRCh38.p12 chr11: 20,626,688-20,654,868	SLC6A5
nsv3921762	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr11: 20,588,259-20,809,826 , GRCh37.p13 chr11: 20,631,683-20,853,250 , GRCh38.p12 chr11: 20,610,137-20,831,704	SLC6A5, NELL1
nsv4729722	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr11: 20,641,021-20,842,894 , GRCh38.p12 chr11: 20,619,475-20,821,348	SLC6A5, NELL1
nsv3898773	copy number variation	1	nstd102	human	Benign	GRCh37 chr11: 20,561,991-20,678,604 , GRCh38.p12 chr11: 20,540,445-20,657,058	SLC6A5, HMGB1P40, 1 more genes
nsv3916031	copy number variation	1	nstd102	human	Uncertain significance	GRCh38 chr11: 20,375,594-20,634,327 , NCBI36 chr11: 20,353,716-20,612,449 , GRCh37 chr11: 20,397,140-20,655,873	SLC6A5, LOC105376584, 3 more genes
nsv4675074	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr11: 20,490,837-20,879,157 , GRCh38.p12 chr11: 20,469,291-20,857,611	SLC6A5, PRMT3, 3 more genes
nsv3913123	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr11: 20,519,068-20,677,028 , NCBI36 chr11: 20,475,644-20,633,604 , GRCh38 chr11: 20,497,522-20,655,482	SLC6A5, LOC105376584, 2 more genes
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	SLC6A5, FAUP4, 2031 more genes
nsv3922794	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 20,101,020-34,485,543 , GRCh38 chr11: 20,079,474-34,463,996 , NCBI36 chr11: 20,057,596-34,442,119	SLC6A5, LOC107984419, 150 more genes
nsv3901577	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 18,536,224-31,923,308 , GRCh38.p12 chr11: 18,514,677-31,901,762	SLC6A5, LOC105376588, 137 more genes
nsv3916542	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr16: 55,457,477-63,841,622 , NCBI36 chr16: 54,048,890-62,433,027 , GRCh37 chr16: 55,491,389-63,875,526	CES1, SNORA46, 139 more genes
nsv6315060	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr16: 53,818,483-57,631,312 , GRCh37.p13 chr16: 53,852,395-57,665,224	LOC105371283, MT1A, 91 more genes
nsv6315493	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 55,054,348-56,403,200 , GRCh38.p12 chr16: 55,020,436-56,369,288	LOC102725116, LOC105371281, 21 more genes
nsv3893233	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 70,864-134,938,470 , GRCh38.p12 chr11: 70,864-135,068,576	SLC6A5, LOC105376598, 2842 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	SLC6A5, RTN3, 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:

Search results

Items: 1 to 20 of 59

Number of Variants: 20

Send to:

Supplemental Content

Find related data

Search details

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

Search results

Items: 1 to 20 of 59

Page of 3

Number of Variants: 20

Page of 3

Supplemental Content

Find related data

Search details

Recent activity