tspan3[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
nsv3893790	copy number variation	1	nstd102	human	Benign	GRCh37 chr15: 77,330,786-77,337,649 , GRCh38.p12 chr15: 77,038,445-77,045,307	TSPAN3
nsv3907537	copy number variation	1	nstd102	human	Benign	GRCh37 chr15: 77,328,269-77,340,328 , GRCh38.p12 chr15: 77,035,928-77,047,986	TSPAN3, PSTPIP1
nsv3898760	copy number variation	1	nstd102	human	Benign	GRCh37 chr15: 77,328,269-77,332,606 , GRCh38.p12 chr15: 77,035,928-77,040,265	TSPAN3, PSTPIP1
nsv3916249	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr15: 21,173,967-100,338,915 , GRCh37.p13 chr15: 23,622,526-102,521,392 , GRCh38.p12 chr15: 23,377,379-101,981,189	TSPAN3, H3P40, 1616 more genes
nsv3919468	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr15: 26,996,912-100,338,915 , GRCh37.p13 chr15: 29,209,620-102,521,392 , GRCh38.p12 chr15: 28,917,417-101,981,189	TSPAN3, RNU6-18P, 1442 more genes
nsv3913942	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr15: 70,025,300-78,705,993 , NCBI36 chr15: 68,104,693-76,785,390 , GRCh37 chr15: 70,317,639-78,998,335	TSPAN3, SNX33, 209 more genes
nsv3913830	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr15: 76,006,154-79,982,417 , NCBI36 chr15: 74,085,550-78,061,814 , GRCh37 chr15: 76,298,495-80,274,759	TSPAN3, LOC105370919, 86 more genes
nsv6637477	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 74,353,736-77,884,397 , GRCh38.p12 chr15: 74,061,395-77,592,055	TSPAN3, PTPN9, 96 more genes
nsv3900281	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 20,016,811-102,493,540 , GRCh38.p12 chr15: 19,811,558-101,953,337	TSPAN3, MYZAP, 1750 more genes
nsv3913581	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr15: 18,323,354-100,338,915 , GRCh37.p13 chr15: 20,063,340-102,521,392 , GRCh38.p12 chr15: 19,858,087-101,981,189	TSPAN3, MIR4513, 1754 more genes
nsv3904086	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 20,071,673-102,461,162 , GRCh38.p12 chr15: 19,866,420-101,920,959	TSPAN3, TMEM202, 1747 more genes
nsv3905138	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 20,733,395-102,511,616 , GRCh38.p12 chr15: 20,528,156-101,971,413	TSPAN3, FES, 1738 more genes
nsv3892955	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr15: 22,770,422-102,429,112 , GRCh38.p12 chr15: 23,319,714-101,888,909	TSPAN3, FAM81A, 1614 more genes
nsv3876912	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 31,115,047-102,354,857 , GRCh38.p12 chr15: 30,822,844-101,814,654	TSPAN3, RNU6-953P, 1385 more genes
nsv3899559	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 41,745,084-102,354,798 , GRCh38.p12 chr15: 41,452,886-101,814,595	TSPAN3, CILP, 1176 more genes
nsv3917589	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 60,120,659-102,461,201 , GRCh38 chr15: 59,828,460-101,920,998 , NCBI36 chr15: 57,907,951-100,278,724	TSPAN3, GAPDHP61, 840 more genes
nsv3895615	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 64,637,227-102,509,910 , GRCh38.p12 chr15: 64,345,028-101,969,707	TSPAN3, KRT18P47, 781 more genes
nsv3899560	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 71,329,220-102,270,758 , GRCh38.p12 chr15: 71,036,881-101,730,555	TSPAN3, KRT8P23, 626 more genes
nsv3915187	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr15: 70,234,344-100,278,724 , GRCh37 chr15: 72,447,290-102,461,201 , GRCh38 chr15: 72,154,949-101,920,998	TSPAN3, LOC102724117, 618 more genes
nsv7148092	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 75,165,490-102,520,892 , GRCh38.p12 chr15: 74,873,149-101,980,689	TSPAN3, RPL9P8, 547 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 32

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Number of Variants: 20

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Supplemental Content

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Search details

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