c12orf56[All Fields] AND 1[has_clinical] - dbVar - NCBI

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Items: 9

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Number of Variants: 9

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv7093395	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr12: 64,609,458-70,352,103 , GRCh38.p12 chr12: 64,215,678-69,958,323	C12ORF56, TODL, 116 more genes
nsv3916302	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr12: 59,587,199-65,248,124 , GRCh37 chr12: 61,300,932-66,961,857 , GRCh38 chr12: 60,907,151-66,568,077	C12ORF56, LOC105369809, 93 more genes
nsv3904242	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr12: 1-133,851,895 , GRCh38.p12 chr12: 45,740-133,265,309	C12ORF56, 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	C12ORF56, 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	C12ORF56, 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	C12ORF56, 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	C12ORF56, OR5BT1P, 2441 more genes
nsv3909395	copy number variation	1	nstd102	human	Benign	GRCh37 chr12: 64,745,313-65,184,236 , GRCh38.p12 chr12: 64,351,533-64,790,456	C12ORF56, RASSF3, 11 more genes
nsv4681587	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr12: 64,173,731-64,895,171 , GRCh38.p12 chr12: 63,779,951-64,501,391	C12ORF56, XPOT, 16 more genes

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