fbrsl1[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
nsv3906021	copy number variation	1	nstd102	human	Benign	GRCh37 chr12: 133,085,227-133,089,054 , GRCh38.p12 chr12: 132,508,641-132,512,468	FBRSL1
nsv3924006	copy number variation	1	nstd102	human	Likely benign	NCBI36 chr12: 131,649,535-131,674,915 , GRCh37 chr12: 133,139,462-133,164,842 , GRCh38 chr12: 132,562,876-132,588,256	FBRSL1, MIR6763
nsv3898043	copy number variation	1	nstd102	human	Benign	GRCh37 chr12: 133,060,725-133,196,596 , GRCh38.p12 chr12: 132,484,139-132,620,010	FBRSL1, MIR6763, 3 more genes
nsv3893538	copy number variation	1	nstd102	human	Benign	GRCh37 chr12: 133,095,629-133,181,425 , GRCh38.p12 chr12: 132,519,043-132,604,839	FBRSL1, MIR6763, 2 more genes
nsv3891122	copy number variation	1	nstd102	human	Benign	GRCh37 chr12: 133,130,292-133,196,619 , GRCh38.p12 chr12: 132,553,706-132,620,033	FBRSL1, LOC105370094, 3 more genes
nsv3907956	copy number variation	1	nstd102	human	Benign	GRCh37 chr12: 133,146,701-133,196,619 , GRCh38.p12 chr12: 132,570,115-132,620,033	FBRSL1, LRCOL1, 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	FBRSL1, GALNT9-AS1, 54 more genes
nsv3913652	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr12: 133,153,200-133,767,986 , GRCh38 chr12: 132,576,614-133,191,400 , NCBI36 chr12: 131,663,273-132,278,059	FBRSL1, PGAM5, 27 more genes
nsv3904242	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr12: 1-133,851,895 , GRCh38.p12 chr12: 45,740-133,265,309	FBRSL1, 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	FBRSL1, 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	FBRSL1, 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	FBRSL1, 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	FBRSL1, 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	FBRSL1, 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	FBRSL1, 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	FBRSL1, 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	FBRSL1, 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	FBRSL1, 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	FBRSL1, 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	FBRSL1, TMEM132C, 192 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 40

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Number of Variants: 20

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Supplemental Content

Find related data

Search details

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