noc4l[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
nsv3897738	copy number variation	1	nstd102	human	Benign	GRCh37 chr12: 132,621,624-132,632,512 , GRCh38.p12 chr12: 132,137,079-132,147,967	NOC4L, DDX51
nsv3906083	copy number variation	1	nstd102	human	Benign	GRCh37 chr12: 132,623,473-132,632,910 , GRCh38.p12 chr12: 132,138,928-132,148,365	NOC4L, DDX51
nsv3893663	copy number variation	1	nstd102	human	Benign	GRCh37 chr12: 132,623,473-132,632,485 , GRCh38.p12 chr12: 132,138,928-132,147,940	NOC4L, DDX51
nsv3896053	copy number variation	1	nstd102	human	Benign	GRCh37 chr12: 132,624,220-132,632,485 , GRCh38.p12 chr12: 132,139,675-132,147,940	NOC4L, DDX51
nsv3893285	copy number variation	1	nstd102	human	Benign	GRCh37 chr12: 132,624,263-132,632,485 , GRCh38.p12 chr12: 132,139,718-132,147,940	NOC4L, DDX51
nsv4456657	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr12: 132,518,782-132,656,253 , GRCh38.p12 chr12: 132,034,237-132,171,708	NOC4L, LOC107987169, 3 more genes
nsv4456242	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr12: 132,523,489-132,656,253 , GRCh38.p12 chr12: 132,038,944-132,171,708	NOC4L, LOC107987169, 3 more genes
nsv3911519	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr12: 130,701,040-132,278,059 , GRCh38 chr12: 131,650,542-133,191,400 , GRCh37 chr12: 132,135,087-133,767,986	NOC4L, GALNT9-AS1, 54 more genes
nsv3904242	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr12: 1-133,851,895 , GRCh38.p12 chr12: 45,740-133,265,309	NOC4L, 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	NOC4L, 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	NOC4L, 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	NOC4L, 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	NOC4L, 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	NOC4L, 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	NOC4L, 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	NOC4L, 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	NOC4L, 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	NOC4L, LOC105370044, 273 more genes
nsv3921145	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr12: 123,929,305-133,767,986 , GRCh38 chr12: 123,444,758-133,191,400 , NCBI36 chr12: 122,495,258-132,278,059	NOC4L, ZNF268, 193 more genes
nsv3911281	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr12: 123,509,825-133,191,400 , GRCh37 chr12: 123,994,372-133,767,986 , NCBI36 chr12: 122,560,325-132,278,059	NOC4L, TMEM132C, 192 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: 1 to 20 of 40

Number of Variants: 20

Send to:

Supplemental Content

Find related data

Search details

Recent activity

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 40

Page of 2

Number of Variants: 20

Page of 2

Supplemental Content

Find related data

Search details

Recent activity