slc17a6[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
nsv3923118	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr11: 22,058,781-22,367,671 , GRCh37 chr11: 22,102,205-22,411,095 , GRCh38 chr11: 22,080,659-22,389,549	SLC17A6, ANO5, 1 more genes
nsv4456878	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr11: 22,045,818-22,472,335 , GRCh38.p12 chr11: 22,024,272-22,450,789	SLC17A6, ANO5, 2 more genes
nsv4675939	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr11: 21,970,753-22,457,449 , GRCh38.p12 chr11: 21,949,207-22,435,903	SLC17A6, ANO5, 1 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	SLC17A6, 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	SLC17A6, LOC107984419, 150 more genes
nsv4455873	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 22,079,154-35,597,645 , GRCh38.p12 chr11: 22,057,608-35,576,097	SLC17A6, DNAJC24, 153 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	SLC17A6, LOC105376588, 137 more genes
nsv3898238	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 21,586,131-33,168,232 , GRCh38.p12 chr11: 21,564,585-33,146,686	SLC17A6, RPS25P1, 114 more genes
nsv3917345	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr11: 22,115,602-25,375,696 , GRCh37 chr11: 22,137,148-25,397,242 , NCBI36 chr11: 22,093,724-25,353,818	SLC17A6, LOC105376588, 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	SLC17A6, 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	SLC17A6, 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	SLC17A6, IGHMBP2, 2829 more genes
nsv3898926	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 230,615-37,698,540 , GRCh38.p12 chr11: 230,615-37,676,990	SLC17A6, OR51L1, 771 more genes
nsv4674879	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 235,934-33,826,995 , GRCh38.p12 chr11: 235,934-33,805,449	SLC17A6, BGLT3, 723 more genes
nsv3906221	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 230,615-31,995,219 , GRCh38.p12 chr11: 230,615-31,973,673	SLC17A6, PCNAP4, 688 more genes
nsv6315535	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 230,615-26,881,146 , GRCh38.p12 chr11: 230,615-26,859,599	SLC17A6, OR52Q1P, 630 more genes
nsv3894525	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 230,615-25,584,362 , GRCh38.p12 chr11: 230,615-25,562,816	SLC17A6, SDHCP4, 620 more genes
nsv4674824	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 11,053,978-34,732,891 , GRCh38.p12 chr11: 11,032,431-34,711,344	SLC17A6, SNORA88, 305 more genes
nsv4675502	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 13,970,757-27,565,888 , GRCh38.p12 chr11: 13,949,210-27,544,341	SLC17A6, MRGPRX5P, 171 more genes
nsv3922877	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr11: 22,173,871-22,931,558 , GRCh37 chr11: 22,217,295-22,974,982 , GRCh38 chr11: 22,195,749-22,953,436	SLC17A6, GAS2, 7 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 27

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Number of Variants: 20

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