slc17a5[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
nsv6312593	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 74,304,790-74,310,174 , GRCh38.p12 chr6: 73,595,067-73,600,451	SLC17A5
nsv4451806	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr6: 73,641,681-73,644,613 , GRCh37 chr6: 74,351,404-74,354,336	SLC17A5
nsv5673779	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 74,345,095-74,346,440 , GRCh38.p12 chr6: 73,635,372-73,636,717	SLC17A5
nsv4683199	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 74,354,120-74,354,336 , GRCh38.p12 chr6: 73,644,397-73,644,613	SLC17A5
nsv6312595	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 74,331,507-74,331,705 , GRCh38.p12 chr6: 73,621,784-73,621,982	SLC17A5
nsv7097589	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 74,320,103-74,320,290 , GRCh38.p12 chr6: 73,610,380-73,610,567	SLC17A5
nsv6312503	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 74,325,018-74,325,190 , GRCh38.p12 chr6: 73,615,295-73,615,467	SLC17A5
nsv5674020	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 74,345,095-74,345,233 , GRCh38.p12 chr6: 73,635,372-73,635,510	SLC17A5
nsv7097087	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 74,363,496-74,363,609 , GRCh38.p12 chr6: 73,653,773-73,653,886	SLC17A5
nsv6314576	insertion	1	nstd102	human	Pathogenic	GRCh37 chr6: 74,348,168-74,348,168 , GRCh38 chr6: 73,638,445-73,638,445	SLC17A5
nsv7097452	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr6: 74,303,101-74,320,122 , GRCh38.p12 chr6: 73,593,378-73,610,399	SLC17A5
nsv4683926	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr6: 74,320,113-74,325,180 , GRCh38.p12 chr6: 73,610,390-73,615,457	SLC17A5
nsv6312594	copy number variation	2	nstd102	human	Pathogenic, Likely pathogenic	GRCh37 chr6: 74,310,064-74,310,174 , GRCh38.p12 chr6: 73,600,341-73,600,451	SLC17A5
nsv3887478	copy number variation	1	nstd102	human	Benign	GRCh37 chr6: 74,340,491-74,348,142 , GRCh38.p12 chr6: 73,630,768-73,638,419	SLC17A5
nsv3886080	copy number variation	1	nstd102	human	Likely benign	GRCh37 chr6: 74,341,681-74,351,732 , GRCh38.p12 chr6: 73,631,958-73,642,009	SLC17A5
nsv7097588	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr6: 74,304,800-74,310,184 , GRCh38.p12 chr6: 73,595,077-73,600,461	SLC17A5
nsv6312408	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 74,304,790-74,354,336 , GRCh38.p12 chr6: 73,595,067-73,644,613	SLC17A5, RPS27P15
nsv3886592	copy number variation	1	nstd102	human	Uncertain significance	GRCh38 chr6: 73,595,057-73,653,906 , GRCh37 chr6: 74,304,780-74,363,629	SLC17A5, RPS27P15
nsv3882998	copy number variation	1	nstd102	human	Benign	GRCh37 chr6: 74,304,415-74,421,677 , GRCh38.p12 chr6: 73,594,692-73,711,954	SLC17A5, RPS27P15, 2 more genes
nsv3873576	copy number variation	1	nstd102	human	Benign	GRCh37 chr6: 74,315,347-74,421,677 , GRCh38.p12 chr6: 73,605,624-73,711,954	SLC17A5, CD109, 2 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 37

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Number of Variants: 20

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