sptan1[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
nsv5381652	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 131,360,669-131,367,766 , GRCh38.p12 chr9: 128,598,390-128,605,487	SPTAN1
nsv4454450	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 131,375,660-131,375,764 , GRCh38 chr9: 128,613,381-128,613,485	SPTAN1
nsv5381653	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr9: 131,362,339-131,362,414 , GRCh38.p12 chr9: 128,600,060-128,600,135	SPTAN1
nsv7097691	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr9: 131,353,736-131,356,672 , GRCh38.p12 chr9: 128,591,457-128,594,393	SPTAN1
nsv6634299	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 131,382,516-131,393,966 , GRCh38.p12 chr9: 128,620,237-128,631,687	SPTAN1, DYNC2I2
nsv3886684	copy number variation	2	nstd102	human	Pathogenic	GRCh38 chr9: 128,632,127-128,640,939 , GRCh37 chr9: 131,394,406-131,403,218	SPTAN1, DYNC2I2
nsv3878327	copy number variation	2	nstd102	human	Uncertain significance, Likely benign	GRCh37 chr9: 131,386,587-131,399,326 , GRCh38 chr9: 128,624,308-128,637,047	SPTAN1, DYNC2I2
nsv5673819	copy number variation	1	nstd102	human	Likely benign	GRCh37 chr9: 131,386,597-131,399,316 , GRCh38.p12 chr9: 128,624,318-128,637,037	SPTAN1, DYNC2I2
nsv7098426	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr9: 131,389,645-131,398,737 , GRCh38.p12 chr9: 128,627,366-128,636,458	SPTAN1, DYNC2I2
nsv7097692	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr9: 131,379,899-131,403,238 , GRCh38.p12 chr9: 128,617,620-128,640,959	SPTAN1, DYNC2I2
nsv7098058	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 131,329,020-131,419,005 , GRCh38.p12 chr9: 128,566,741-128,656,726	SPTAN1, VTI1BP4, 1 more genes
nsv3899776	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 129,370,440-133,866,894 , GRCh38.p12 chr9: 126,608,161-130,991,507	SPTAN1, FNBP1, 136 more genes
nsv3917587	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr9: 127,795,683-131,484,475 , GRCh38 chr9: 125,993,583-129,682,375 , GRCh37 chr9: 128,755,862-132,444,654	SPTAN1, DYNC2I2, 115 more genes
nsv3924370	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr9: 126,857,965-130,440,046 , GRCh38 chr9: 125,055,865-128,637,946 , GRCh37 chr9: 127,818,144-131,400,225	SPTAN1, MVB12B, 97 more genes
nsv3918361	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr9: 129,676,681-132,287,019 , GRCh38 chr9: 127,874,581-130,421,811 , GRCh37 chr9: 130,636,860-133,297,198	SPTAN1, GOLGA2, 89 more genes
nsv3903209	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 130,390,139-132,760,275 , GRCh38.p12 chr9: 127,627,860-129,997,996	SPTAN1, PTRH1, 99 more genes
nsv3909918	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr9: 129,933,505-131,594,414 , GRCh37.p13 chr9: 130,893,684-132,554,593 , GRCh38.p12 chr9: 128,131,405-129,792,314	SPTAN1, C9orf50, 65 more genes
nsv4675731	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 130,957,344-132,310,210 , GRCh38.p12 chr9: 128,195,065-129,547,931	SPTAN1, PTPA, 55 more genes
nsv3914825	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr9: 129,873,497-130,897,002 , GRCh37.p13 chr9: 130,833,676-131,857,181 , GRCh38.p12 chr9: 128,071,397-129,094,902	SPTAN1, RNU7-171P, 49 more genes
nsv4768374	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 130,412,438-131,423,964 , GRCh38.p12 chr9: 127,650,159-128,661,685	SPTAN1, COQ4, 53 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 57

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Number of Variants: 20

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