wif1[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
nsv3905108	copy number variation	1	nstd102	human	Benign	GRCh37 chr12: 65,437,106-65,481,947 , GRCh38.p12 chr12: 65,043,326-65,088,167	WIF1
nsv3907669	copy number variation	1	nstd102	human	Benign	GRCh37 chr12: 65,507,997-65,641,261 , GRCh38.p12 chr12: 65,114,217-65,247,481	WIF1, APOOP3, 1 more genes
nsv6112755	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr12: 65,251,705-75,263,379 , GRCh38.p12 chr12: 64,857,925-74,869,599	WIF1, LINC02421, 144 more genes
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	WIF1, 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	WIF1, LOC105369809, 93 more genes
nsv7094153	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr12: 64,849,651-65,857,102 , GRCh38.p12 chr12: 64,455,871-65,463,322	WIF1, GNS, 18 more genes
nsv3904242	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr12: 1-133,851,895 , GRCh38.p12 chr12: 45,740-133,265,309	WIF1, 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	WIF1, 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	WIF1, 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	WIF1, 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	WIF1, OR5BT1P, 2441 more genes
nsv4674998	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr12: 65,029,704-65,589,195 , GRCh38.p12 chr12: 64,635,924-65,195,415	WIF1, LOC107984522, 10 more genes

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