vsig10[All Fields] AND 1[has_clinical] - dbVar - NCBI

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Number of Variants: 14

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv3898298	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr12: 116,028,864-118,791,808 , GRCh38.p12 chr12: 115,591,059-118,354,003	VSIG10, LOC101928274, 38 more genes
nsv3904242	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr12: 1-133,851,895 , GRCh38.p12 chr12: 45,740-133,265,309	VSIG10, 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	VSIG10, 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	VSIG10, 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	VSIG10, 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	VSIG10, 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	VSIG10, 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	VSIG10, LOC105370080, 376 more genes
nsv6290239	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr12: 117,461,902-133,841,395 , GRCh38.p12 chr12: 117,024,097-133,264,809	VSIG10, ACADS, 356 more genes
nsv3906446	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr12: 118,486,842-120,995,382 , GRCh38.p12 chr12: 118,049,037-120,557,579	VSIG10, COX6A1, 63 more genes
nsv3894629	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr12: 118,014,801-118,716,129 , GRCh38.p12 chr12: 117,576,996-118,278,324	VSIG10, LOC101928274, 7 more genes
nsv4455668	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr12: 116,718,607-119,728,623 , GRCh38.p12 chr12: 116,280,802-119,290,818	VSIG10, LINC00934, 53 more genes
nsv4675388	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr12: 117,858,408-118,668,114 , GRCh38.p12 chr12: 117,420,603-118,230,309	VSIG10, LOC101928274, 7 more genes
nsv3898723	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr12: 118,258,061-118,726,805 , GRCh38.p12 chr12: 117,820,256-118,289,000	VSIG10, LOC101928274, 7 more genes

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vsig10[All Fields] AND 1[has_clinical] (15)
dbVar
Pseudomonas syringae pv. actinidiae strain C24 BV329_233, whole genome shotgun s...
Pseudomonas syringae pv. actinidiae strain C24 BV329_233, whole genome shotgun sequence
gi|1187894179|gb|MTHS01000233.1||gn :MTHS01|BV329_233

Nucleotide

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