slc2a13[All Fields] AND 1[has_clinical] - dbVar

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Number of Variants: 20

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv3894690	copy number variation	1	nstd102	human	Benign	GRCh37 chr12: 40,362,276-40,413,698 , GRCh38.p12 chr12: 39,968,474-40,019,896	SLC2A13
nsv3916943	copy number variation	1	nstd102	human	Likely benign	GRCh38 chr12: 39,934,307-39,976,881 , NCBI36 chr12: 38,614,376-38,656,950 , GRCh37 chr12: 40,328,109-40,370,683	SLC2A13
nsv3903258	copy number variation	1	nstd102	human	Benign	GRCh37 chr12: 40,492,814-40,499,934 , GRCh38.p12 chr12: 40,099,012-40,106,132	SLC2A13
nsv3893173	copy number variation	1	nstd102	human	Benign	GRCh37 chr12: 40,498,190-40,499,934 , GRCh38.p12 chr12: 40,104,388-40,106,132	SLC2A13
nsv3898368	copy number variation	1	nstd102	human	Benign	GRCh37 chr12: 40,498,190-40,499,908 , GRCh38.p12 chr12: 40,104,388-40,106,106	SLC2A13
nsv3909414	copy number variation	1	nstd102	human	Benign	GRCh37 chr12: 40,498,190-40,499,803 , GRCh38.p12 chr12: 40,104,388-40,106,001	SLC2A13
nsv3902827	copy number variation	1	nstd102	human	Benign	GRCh37 chr12: 40,498,683-40,499,803 , GRCh38.p12 chr12: 40,104,881-40,106,001	SLC2A13
nsv3891293	copy number variation	1	nstd102	human	Benign	GRCh37 chr12: 40,499,495-40,499,908 , GRCh38.p12 chr12: 40,105,693-40,106,106	SLC2A13
nsv3893148	copy number variation	1	nstd102	human	Benign	GRCh37 chr12: 40,499,634-40,499,934 , GRCh38.p12 chr12: 40,105,832-40,106,132	SLC2A13
nsv3901183	copy number variation	1	nstd102	human	Benign	GRCh37 chr12: 40,182,606-40,236,374 , GRCh38.p12 chr12: 39,788,804-39,842,572	SLC2A13, REDIC1
nsv3892066	copy number variation	1	nstd102	human	Benign	GRCh37 chr12: 40,192,820-40,235,645 , GRCh38.p12 chr12: 39,799,018-39,841,843	SLC2A13, REDIC1
nsv6637205	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr12: 40,272,679-40,452,284 , GRCh38.p12 chr12: 39,878,877-40,058,482	SLC2A13, REDIC1
nsv4676088	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr12: 40,250,496-40,313,865 , GRCh38.p12 chr12: 39,856,694-39,920,063	SLC2A13, REDIC1
nsv3891103	copy number variation	1	nstd102	human	Benign	GRCh37 chr12: 40,413,698-40,536,061 , GRCh38.p12 chr12: 40,019,896-40,142,259	SLC2A13, RPL30P13, 2 more genes
nsv4456562	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr12: 39,577,315-40,582,797 , GRCh38.p12 chr12: 39,183,513-40,188,995	SLC2A13, LINC02471, 9 more genes
nsv3904242	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr12: 1-133,851,895 , GRCh38.p12 chr12: 45,740-133,265,309	SLC2A13, RNA5SP369, 2454 more genes
nsv3905447	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr12: 173,787-133,777,902 , GRCh38.p12 chr12: 64,621-133,201,316	SLC2A13, LOH12CR2, 2452 more genes
nsv3897722	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr12: 191,619-133,777,645 , GRCh38.p12 chr12: 82,453-133,201,059	SLC2A13, RNU4ATAC16P, 2452 more genes
nsv3914194	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr12: 100,698-132,283,466 , GRCh37 chr12: 282,465-133,773,393 , GRCh38 chr12: 121,271-133,196,807	SLC2A13, BTG1P1, 2451 more genes
nsv3904719	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr12: 621,220-133,779,118 , GRCh38.p12 chr12: 512,054-133,202,532	SLC2A13, OR5BT1P, 2441 more genes

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Number of Variants: 20

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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 35

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Number of Variants: 20

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Supplemental Content

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