ngf[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
nsv3897769	copy number variation	1	nstd102	human	Benign	GRCh37 chr12: 5,577,867-5,626,158 , GRCh38.p12 chr12: 5,468,701-5,516,992	NTF3
nsv3911463	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr12: 5,577,474-5,625,372 , GRCh38 chr12: 5,468,308-5,516,206 , NCBI36 chr12: 5,447,735-5,495,633	NTF3
nsv3905451	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr12: 5,578,947-5,603,350 , GRCh38.p12 chr12: 5,469,781-5,494,184	NTF3
nsv3901609	copy number variation	1	nstd102	human	Benign	GRCh37 chr12: 5,550,738-5,690,885 , GRCh38.p12 chr12: 5,441,572-5,581,719	ANO2, NTF3
nsv3894961	copy number variation	1	nstd102	human	Benign	GRCh37 chr12: 5,550,738-5,690,626 , GRCh38.p12 chr12: 5,441,572-5,581,460	NTF3, ANO2
nsv5381204	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr1: 115,828,681-115,829,426 , GRCh38.p12 chr1: 115,286,060-115,286,805	NGF, NGF-AS1
nsv7095317	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr1: 115,828,691-115,829,416 , GRCh38.p12 chr1: 115,286,070-115,286,795	NGF, NGF-AS1
nsv5381058	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 102,021,465-119,737,478 , GRCh38.p12 chr1: 101,555,909-119,194,855	NGF, AMYP1, 320 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	TSPAN9, RNU6-174P, 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	LRTM2, FOXM1, 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	SLC6A13, RPL18P9, 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	LOC105369595, KDM5A, 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	LOC107987182, LOC100533654, 106 more genes
nsv3877365	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 47,851-249,228,449 , GRCh38.p12 chr1: 47,851-248,934,250	NGF, MARK1, 4930 more genes
nsv3885206	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 82,154-249,218,992 , GRCh38.p12 chr1: 82,154-248,924,793	NGF, SNAP47, 4927 more genes
nsv3884414	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr1: 849,467-249,224,684 , GRCh38.p12 chr1: 914,087-248,930,485	NGF, RNU1-153P, 4887 more genes
nsv3904242	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr12: 1-133,851,895 , GRCh38.p12 chr12: 45,740-133,265,309	RNA5SP369, ST13P22, 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	LOH12CR2, OR8S21P, 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	RNU4ATAC16P, PIGAP1, 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	BTG1P1, LOC105370073, 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 72

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Number of Variants: 20

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