Gp96[All Fields] AND 1[has_clinical] - dbVar - NCBI

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Number of Variants: 12

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv6291583	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr12: 104,230,462-111,984,801 , GRCh38.p12 chr12: 103,836,684-111,546,997	LOC105369964, LOC644746, 147 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
nsv3904719	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr12: 621,220-133,779,118 , GRCh38.p12 chr12: 512,054-133,202,532	OR5BT1P, RECQL, 2441 more genes
nsv3924338	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr12: 89,962,226-108,055,398 , GRCh38 chr12: 91,044,318-109,133,210 , GRCh37 chr12: 91,438,095-109,571,015	NUP37, TTC41P, 295 more genes
nsv3893927	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr12: 103,044,333-111,639,805 , GRCh38.p12 chr12: 102,650,555-111,202,001	ACACB, ASCL1, 150 more genes
nsv4456580	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr12: 102,414,522-105,845,768 , GRCh38.p12 chr12: 102,020,744-105,451,990	HCFC2, MIR3652, 50 more genes
nsv3923579	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr12: 102,418,033-103,644,780 , GRCh38 chr12: 103,500,125-104,726,872 , GRCh37 chr12: 103,893,903-105,120,650	LOC105369949, LINC02401, 23 more genes
nsv3907610	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr12: 100,580,198-105,804,075 , GRCh38.p12 chr12: 100,186,420-105,410,297	ASCL1, C12orf75-AS1, 87 more genes
nsv6637829	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr12: 103,588,380-105,161,579 , GRCh38.p12 chr12: 103,194,602-104,767,801	TDG, MIR3922, 24 more genes

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