slc35c1[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
nsv4682898	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr11: 45,827,333-45,932,533 , GRCh38.p12 chr11: 45,805,782-45,910,982	SLC35C1, MAPK8IP1, 3 more genes
nsv6309365	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr11: 45,827,353-45,932,533 , GRCh38.p12 chr11: 45,805,802-45,910,982	SLC35C1, FREY1, 3 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	SLC35C1, FAUP4, 2031 more genes
nsv3922177	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr11: 35,663,578-46,959,820 , GRCh37 chr11: 35,685,126-46,981,371 , NCBI36 chr11: 35,641,702-46,937,947	SLC35C1, MIR3160-2, 122 more genes
nsv3913842	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 39,200,802-49,157,287 , NCBI36 chr11: 39,157,378-49,113,863 , GRCh38 chr11: 39,179,252-49,135,735	SLC35C1, MIR3160-1, 162 more genes
nsv3924778	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr11: 41,118,322-48,643,003 , GRCh37 chr11: 41,139,872-48,664,555 , NCBI36 chr11: 41,096,448-48,621,131	SLC35C1, F2, 140 more genes
nsv6291196	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 40,117,145-46,920,718 , GRCh38.p12 chr11: 40,095,595-46,899,167	SLC35C1, LINC02687, 86 more genes
nsv3921841	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr11: 42,531,785-46,092,919 , GRCh37 chr11: 42,575,209-46,136,343 , GRCh38 chr11: 42,553,659-46,114,792	SLC35C1, PEX16, 51 more genes
nsv3919271	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr11: 44,136,593-46,121,139 , NCBI36 chr11: 44,114,719-46,099,266 , GRCh37 chr11: 44,158,143-46,142,690	SLC35C1, LOC105376646, 31 more genes
nsv6309196	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 45,827,353-46,401,497 , GRCh38.p12 chr11: 45,805,802-46,379,947	SLC35C1, LINC02710, 14 more genes
nsv997191	copy number variation	1	nstd45	human	Pathogenic	GRCh37 chr11: 43,894,800-46,152,450 , GRCh38.p12 chr11: 43,873,250-46,130,899	SLC35C1, CRY2, 39 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	SLC35C1, 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	SLC35C1, RTN3, 2833 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	SLC35C1, IGHMBP2, 2829 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	SLC35C1, PYGM, 2125 more genes
nsv6315474	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 43,607,886-61,466,671 , GRCh38.p12 chr11: 43,586,336-61,699,199	SLC35C1, TRR-TCT3-2, 494 more genes
nsv5380725	copy number variation	2	nstd102	human	Pathogenic, Uncertain significance	GRCh37 chr11: 45,827,353-47,804,770 , GRCh38.p12 chr11: 45,805,802-47,783,218	SLC35C1, MIR4688, 58 more genes
nsv3914563	copy number variation	1	nstd102	human	Likely pathogenic	NCBI36 chr11: 42,705,681-49,113,863 , GRCh37 chr11: 42,749,105-49,157,287 , GRCh38 chr11: 42,727,555-49,135,735	SLC35C1, ACP2, 143 more genes
nsv6291214	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr11: 45,675,636-45,850,138 , GRCh38.p12 chr11: 45,654,086-45,828,587	SLC35C1, LINC02690, 4 more genes
nsv4729649	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr11: 44,266,593-46,123,796 , GRCh38.p12 chr11: 44,245,043-46,102,245	SLC35C1, LOC105376654, 31 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 21

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 21

Page of 2

Number of Variants: 20

Page of 2

Supplemental Content

Find related data

Search details

Recent activity