snx8[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
nsv3923668	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr7: 2,302,956-2,377,332 , GRCh38 chr7: 2,263,321-2,337,697	SNX8, IMMP1LP3
nsv4578656	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr7: 2,294,689-2,317,940 , GRCh38.p12 chr7: 2,255,054-2,278,305	SNX8, MIR6836
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	SNX8, 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	SNX8, RNU6-215P, 120 more genes
nsv4456136	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 36,616-4,298,168 , GRCh38.p12 chr7: 36,616-4,258,536	SNX8, LOC442497, 85 more genes
nsv3894332	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 1,201,674-5,175,651 , GRCh38.p12 chr7: 1,162,038-5,136,020	SNX8, FOXK1, 70 more genes
nsv3898790	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 43,360-3,642,604 , GRCh38.p12 chr7: 43,360-3,602,972	SNX8, RPL21P72, 83 more genes
nsv3911664	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr7: 54,185-3,324,143 , GRCh37 chr7: 54,185-3,363,775 , NCBI36 chr7: 149,268-3,330,301	SNX8, MIR6836, 81 more genes
nsv3912605	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr7: 54,165-3,258,775 , NCBI36 chr7: 149,248-3,264,933 , GRCh37 chr7: 54,165-3,298,407	SNX8, LOC100129603, 80 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	SNX8, 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	SNX8, 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	SNX8, 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	SNX8, 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	SNX8, 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	SNX8, 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	SNX8, 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	SNX8, 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	SNX8, ZNF12, 389 more genes
nsv3916518	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 1,737,760-27,246,914 , NCBI36 chr7: 1,704,286-27,213,439 , GRCh38 chr7: 1,698,124-27,207,295	SNX8, LOC105375156, 365 more genes
nsv3913671	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr7: 140,213-25,227,309 , GRCh38 chr7: 45,130-25,221,165 , GRCh37 chr7: 45,130-25,260,784	SNX8, UNCX, 363 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 54

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Number of Variants: 20

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Supplemental Content

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