slc29a4[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
nsv4455330	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr7: 5,295,291-5,348,925 , GRCh38.p12 chr7: 5,255,660-5,309,294	SLC29A4, TNRC18
nsv3896682	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr7: 5,198,327-5,347,753 , GRCh38.p12 chr7: 5,158,696-5,308,122	SLC29A4, WIPI2, 2 more genes
nsv4729471	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr7: 5,268,201-5,397,816 , GRCh38.p12 chr7: 5,228,570-5,358,185	SLC29A4, WIPI2, 1 more genes
nsv6289945	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr7: 5,239,584-5,401,976 , GRCh38.p12 chr7: 5,199,953-5,362,345	SLC29A4, WIPI2, 1 more genes
nsv3919826	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 54,185-159,075,079 , GRCh38 chr7: 54,185-159,282,390 , NCBI36 chr7: 149,268-158,767,840	SLC29A4, RNU6-438P, 2682 more genes
nsv3920006	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 45,130-5,920,006 , GRCh38 chr7: 45,130-5,880,375 , NCBI36 chr7: 140,213-5,886,532	SLC29A4, RNU6-215P, 120 more genes
nsv3912217	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr7: 5,062,000-6,692,258 , GRCh37 chr7: 5,101,631-6,731,889 , NCBI36 chr7: 5,068,157-6,698,414	SLC29A4, RBAK-RBAKDN, 45 more genes
nsv6637083	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 4,655,928-5,990,874 , GRCh38.p12 chr7: 4,616,297-5,951,243	SLC29A4, RN7SL556P, 34 more genes
nsv3924886	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 5,101,631-5,864,814 , GRCh38 chr7: 5,062,000-5,825,183 , NCBI36 chr7: 5,068,157-5,831,340	SLC29A4, LINC02983, 18 more genes
nsv3919366	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 5,157,150-5,920,006 , GRCh38 chr7: 5,117,519-5,880,375 , NCBI36 chr7: 5,123,676-5,886,532	SLC29A4, FBXL18, 17 more genes
nsv6290245	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 5,096,876-5,569,338 , GRCh38.p12 chr7: 5,057,245-5,529,707	SLC29A4, MIR589, 12 more genes
nsv3894780	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 10,704-159,122,532 , GRCh38.p12 chr7: 10,704-159,329,842	SLC29A4, RNU6-565P, 2684 more genes
nsv4455091	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 10,365-159,119,707 , GRCh38.p12 chr7: 10,365-159,327,017	SLC29A4, RPL23AP51, 2684 more genes
nsv3909087	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 44,935-159,126,310 , GRCh38.p12 chr7: 44,935-159,333,620	SLC29A4, MNX1-AS2, 2682 more genes
nsv3908592	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr7: 43,361-159,119,707 , GRCh38.p12 chr7: 43,361-159,327,017	SLC29A4, TRGV3, 2682 more genes
nsv3915802	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 54,185-41,915,483 , GRCh38 chr7: 54,185-41,875,885 , NCBI36 chr7: 149,268-41,882,008	SLC29A4, RPL23AP52, 638 more genes
nsv3918785	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 54,185-37,129,317 , NCBI36 chr7: 149,268-37,095,842 , GRCh38 chr7: 54,185-37,089,712	SLC29A4, MMD2, 554 more genes
nsv3903410	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 704,573-29,257,946 , GRCh38.p12 chr7: 664,936-29,218,330	SLC29A4, LOC100131264, 422 more genes
nsv3922329	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 43,360-27,236,023 , GRCh38 chr7: 43,360-27,196,404 , NCBI36 chr7: 138,443-27,202,548	SLC29A4, LOC401312, 411 more genes
nsv3916683	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 54,185-26,867,253 , NCBI36 chr7: 149,268-26,833,778 , GRCh38 chr7: 54,185-26,827,634	SLC29A4, ZNF12, 389 more genes

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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 50

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Number of Variants: 20

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