anapc5[All Fields] AND 1[has_clinical] - dbVar

loading data ...

Number of Variants: 20

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv3923612	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr12: 120,718,786-127,500,215 , GRCh37 chr12: 121,156,589-127,984,760 , NCBI36 chr12: 119,640,972-126,550,713	ANAPC5, NCOR2, 161 more genes
nsv3921651	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr12: 119,426,254-121,510,218 , GRCh37 chr12: 120,941,871-122,944,265 , GRCh38 chr12: 120,504,068-122,459,718	ANAPC5, ACADS, 58 more genes
nsv3922210	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr12: 120,248,060-121,556,029 , GRCh37 chr12: 121,956,483-122,990,076 , GRCh38 chr12: 121,325,874-122,505,529	ANAPC5, KDM2B-DT, 31 more genes
nsv3904242	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr12: 1-133,851,895 , GRCh38.p12 chr12: 45,740-133,265,309	ANAPC5, 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	ANAPC5, 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	ANAPC5, 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	ANAPC5, BTG1P1, 2451 more genes
nsv3904719	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr12: 621,220-133,779,118 , GRCh38.p12 chr12: 512,054-133,202,532	ANAPC5, OR5BT1P, 2441 more genes
nsv3913894	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr12: 113,190,591-132,287,975 , GRCh38 chr12: 114,268,403-133,201,316 , GRCh37 chr12: 114,706,208-133,777,902	ANAPC5, TAOK3, 386 more genes
nsv3924220	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr12: 115,131,583-133,166,920 , NCBI36 chr12: 114,053,771-132,253,579 , GRCh37 chr12: 115,569,388-133,743,506	ANAPC5, LOC105370080, 376 more genes
nsv3920557	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr12: 118,603,264-133,758,908 , GRCh38 chr12: 118,165,459-133,182,322 , NCBI36 chr12: 117,087,647-132,268,981	ANAPC5, TMED2, 339 more genes
nsv3896575	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr12: 120,367,241-133,777,645 , GRCh38.p12 chr12: 119,929,437-133,201,059	ANAPC5, LOC107984448, 306 more genes
nsv3923347	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr12: 119,619,858-132,289,149 , GRCh37 chr12: 121,135,475-133,779,076 , GRCh38 chr12: 120,697,672-133,202,490	ANAPC5, LOC105370044, 273 more genes
nsv6290239	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr12: 117,461,902-133,841,395 , GRCh38.p12 chr12: 117,024,097-133,264,809	ANAPC5, ACADS, 356 more genes
nsv3914229	copy number variation	1	nstd102	human	Likely benign	NCBI36 chr12: 120,033,179-120,248,060 , GRCh37 chr12: 121,548,796-121,763,677 , GRCh38 chr12: 121,110,993-121,325,874	ANAPC5, P2RX4, 4 more genes
nsv6637167	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr12: 121,551,496-121,771,295 , GRCh38.p12 chr12: 121,113,693-121,333,492	ANAPC5, CAMKK2, 4 more genes
nsv3922077	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr12: 118,209,081-121,689,052 , GRCh38 chr12: 119,286,893-122,638,552 , GRCh37 chr12: 119,724,698-123,123,099	ANAPC5, RPS20P31, 94 more genes
nsv7148095	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr12: 121,341,598-124,103,434 , GRCh38.p12 chr12: 120,903,795-123,618,887	ANAPC5, MLXIP, 82 more genes
nsv3890662	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr12: 121,441,298-122,107,345 , GRCh38.p12 chr12: 121,003,495-121,669,439	ANAPC5, MORN3, 17 more genes
nsv3910686	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr12: 119,868,295-120,506,227 , GRCh37.p13 chr12: 121,383,912-122,021,844 , GRCh38.p12 chr12: 120,946,109-121,583,939	ANAPC5, LOC105370030, 15 more genes

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

Send to:

Search results

Items: 20

Number of Variants: 20

Send to:

Supplemental Content

Find related data

Search details

Recent activity