slc29a3[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
nsv7093727	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 73,111,299-73,122,365 , GRCh38.p12 chr10: 71,351,542-71,362,608	SLC29A3
nsv7093645	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 73,121,691-73,122,365 , GRCh38.p12 chr10: 71,361,934-71,362,608	SLC29A3
nsv7093644	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 73,115,818-73,116,020 , GRCh38.p12 chr10: 71,356,061-71,356,263	SLC29A3
nsv3874283	copy number variation	1	nstd102	human	Uncertain significance	GRCh38 chr10: 71,319,290-71,323,074 , GRCh37 chr10: 73,079,047-73,082,831	SLC29A3
nsv6309005	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr10: 73,079,067-73,082,831 , GRCh38.p12 chr10: 71,319,310-71,323,074	SLC29A3
nsv3905825	copy number variation	1	nstd102	human	Benign	GRCh37 chr10: 73,062,048-73,100,480 , GRCh38.p12 chr10: 71,302,291-71,340,723	SLC29A3, UNC5B, 1 more genes
nsv7137209	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 12,829,206-135,427,143 , GRCh38.p12 chr10: 12,787,207-133,613,639	SLC29A3, RNU7-12P, 1876 more genes
nsv3922335	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 60,196,226-76,174,974 , GRCh38 chr10: 58,436,466-74,415,216 , NCBI36 chr10: 59,866,232-75,844,980	SLC29A3, UNC5B-AS1, 250 more genes
nsv3917822	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr10: 63,402,579-75,296,099 , GRCh37 chr10: 65,162,339-77,055,857 , NCBI36 chr10: 64,832,345-76,725,863	SLC29A3, MYL6P3, 220 more genes
nsv6314185	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 68,735,254-78,885,714 , GRCh38.p12 chr10: 66,975,496-77,125,956	SLC29A3, SLC25A16, 204 more genes
nsv3906389	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 73,232-135,524,321 , GRCh38.p12 chr10: 27,296-133,786,996	SLC29A3, LOC100419870, 2105 more genes
nsv3891157	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 98,087-135,477,883 , GRCh38.p12 chr10: 52,147-133,740,558	SLC29A3, AGAP14P, 2097 more genes
nsv3902271	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr10: 100,027-135,427,143 , GRCh38.p12 chr10: 54,087-133,613,639	SLC29A3, ANXA11, 2085 more genes
nsv3891958	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 93,297-135,378,918 , GRCh38.p12 chr10: 47,357-133,565,414	SLC29A3, TUBB8, 2085 more genes
nsv7137211	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 11,138,692-135,427,143 , GRCh38.p12 chr10: 11,096,729-133,613,639	SLC29A3, EXOC6, 1906 more genes
nsv3924859	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr10: 52,159,133-88,896,941 , GRCh38 chr10: 50,729,367-87,147,204 , GRCh37 chr10: 52,489,127-88,906,961	SLC29A3, BMS1P4-AGAP5, 471 more genes
nsv3917047	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr10: 42,500,760-75,145,672 , GRCh37 chr10: 43,180,754-75,475,666 , GRCh38 chr10: 42,685,306-73,715,908	SLC29A3, SLC9A3P3, 476 more genes
nsv3891070	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 69,040,366-93,194,993 , GRCh38.p12 chr10: 67,280,608-91,435,236	SLC29A3, NRG3-AS1, 441 more genes
nsv3917966	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr10: 68,626,331-80,851,819 , GRCh37 chr10: 68,956,325-81,181,813 , GRCh38 chr10: 67,196,567-79,422,057	SLC29A3, LINC02640, 231 more genes
nsv3921517	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr10: 72,641,730-73,043,923 , GRCh37 chr10: 72,971,724-73,373,917 , GRCh38 chr10: 71,211,967-71,614,160	SLC29A3, UNC5B, 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 24

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Number of Variants: 20

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Supplemental Content

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