tulp3[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
nsv3892613	copy number variation	1	nstd102	human	Benign	GRCh37 chr12: 2,973,615-3,034,490 , GRCh38.p12 chr12: 2,864,449-2,925,324	TULP3, RHNO1, 1 more genes
nsv4457052	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr12: 173,786-6,346,092 , GRCh38.p12 chr12: 64,620-6,236,926	TULP3, TSPAN9, 118 more genes
nsv3906935	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr12: 173,786-6,201,932 , GRCh38.p12 chr12: 64,620-6,092,766	TULP3, LRTM2, 113 more genes
nsv3907924	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr12: 173,786-6,039,841 , GRCh38.p12 chr12: 64,620-5,930,675	TULP3, SLC6A13, 111 more genes
nsv3901202	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr12: 173,786-5,952,112 , GRCh38.p12 chr12: 64,620-5,842,946	TULP3, LOC105369595, 110 more genes
nsv3910984	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr12: 179,323-5,786,793 , GRCh37 chr12: 309,062-5,916,532 , GRCh38 chr12: 199,896-5,807,366	TULP3, LOC107987182, 106 more genes
nsv4729176	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr12: 191,242-4,683,495 , GRCh38.p12 chr12: 82,076-4,574,329	TULP3, RPL18P9, 92 more genes
nsv3912688	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr12: 282,465-4,529,751 , NCBI36 chr12: 59,839-4,400,012 , GRCh38 chr12: 80,412-4,420,585	TULP3, RPL23AP14, 88 more genes
nsv3916748	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr12: 282,465-4,114,078 , NCBI36 chr12: 33,854-3,984,339 , GRCh38 chr12: 54,427-4,004,912	TULP3, LAMP1P1, 79 more genes
nsv3909356	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr12: 173,786-4,105,910 , GRCh38.p12 chr12: 64,620-3,996,744	TULP3, ITFG2-AS1, 79 more genes
nsv3910104	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr12: 121,255-3,968,447 , NCBI36 chr12: 100,682-3,947,874 , GRCh37 chr12: 282,465-4,077,613	TULP3, DCP1B, 78 more genes
nsv3894971	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr12: 222,888-3,931,052 , GRCh38.p12 chr12: 113,722-3,821,886	TULP3, CRACR2A, 75 more genes
nsv3914833	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr12: 282,465-3,748,769 , NCBI36 chr12: 33,854-3,619,030 , GRCh38 chr12: 54,427-3,639,603	TULP3, NRIP2, 73 more genes
nsv3920691	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr12: 282,465-3,112,486 , NCBI36 chr12: 100,682-2,982,747 , GRCh38 chr12: 121,255-3,003,320	TULP3, CACNA1C-AS2, 60 more genes
nsv6313933	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr12: 2,790,077-5,325,700 , GRCh38.p12 chr12: 2,680,911-5,216,534	TULP3, OTUD4P1, 59 more genes
nsv3920162	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr12: 2,472,155-4,809,269 , GRCh37 chr12: 2,601,894-4,939,008 , GRCh38 chr12: 2,492,728-4,829,842	TULP3, RPL23AP14, 55 more genes
nsv3904242	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr12: 1-133,851,895 , GRCh38.p12 chr12: 45,740-133,265,309	TULP3, RNA5SP369, 2454 more genes
nsv3905447	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr12: 173,787-133,777,902 , GRCh38.p12 chr12: 64,621-133,201,316	TULP3, LOH12CR2, 2452 more genes
nsv3897722	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr12: 191,619-133,777,645 , GRCh38.p12 chr12: 82,453-133,201,059	TULP3, RNU4ATAC16P, 2452 more genes
nsv3914194	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr12: 100,698-132,283,466 , GRCh37 chr12: 282,465-133,773,393 , GRCh38 chr12: 121,271-133,196,807	TULP3, BTG1P1, 2451 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 64

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Number of Variants: 20

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