nacc1[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
nsv6310452	copy number variation	1	nstd102	human	Uncertain significance	GRCh38 chr19: 13,135,343-13,135,399 , GRCh37 chr19: 13,246,157-13,246,213	NACC1
nsv3915970	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr19: 13,006,480-13,255,500 , GRCh37 chr19: 13,145,480-13,394,500 , GRCh38 chr19: 13,034,666-13,283,686	NACC1, CACNA1A, 7 more genes
nsv3922964	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr19: 10,319,474-13,777,860 , NCBI36 chr19: 10,291,150-13,749,674 , GRCh37 chr19: 10,430,150-13,888,674	NACC1, SWSAP1, 164 more genes
nsv3924466	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr19: 11,496,978-14,126,833 , GRCh38 chr19: 11,525,163-14,155,021 , GRCh37 chr19: 11,635,978-14,265,833	NACC1, JUNB, 135 more genes
nsv3912480	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr19: 12,580,427-14,742,673 , GRCh37 chr19: 12,691,241-14,853,485 , NCBI36 chr19: 12,552,241-14,714,485	NACC1, GET3, 100 more genes
nsv3907864	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr19: 12,574,343-14,726,197 , GRCh38.p12 chr19: 12,463,529-14,615,385	NACC1, WDR83, 105 more genes
nsv3919036	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr19: 11,628,640-13,336,101 , NCBI36 chr19: 11,489,640-13,197,101 , GRCh38 chr19: 11,517,825-13,225,287	NACC1, ZNF763, 105 more genes
nsv6291633	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr19: 12,697,728-14,111,313 , GRCh38.p12 chr19: 12,586,914-14,000,501	NACC1, RN7SL619P, 67 more genes
nsv3907118	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr19: 12,204,632-13,497,073 , GRCh38.p12 chr19: 12,093,817-13,386,259	NACC1, ZNF625, 73 more genes
nsv4457524	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr19: 12,354,642-13,424,014 , GRCh38.p12 chr19: 12,243,827-13,313,200	NACC1, BEST2, 64 more genes
nsv6310462	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr19: 12,757,434-13,617,038 , GRCh38.p12 chr19: 12,646,620-13,506,224	NACC1, DHPS, 42 more genes
nsv3917896	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr19: 12,946,208-13,380,400 , GRCh38 chr19: 12,974,394-13,408,586 , GRCh37 chr19: 13,085,208-13,519,400	NACC1, CACNA1A, 9 more genes
nsv3880638	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr19: 13,106,632-13,428,155 , GRCh38.p12 chr19: 12,995,818-13,317,341	NACC1, STX10, 8 more genes
nsv3904885	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr19: 68,029-59,110,290 , GRCh38.p12 chr19: 68,029-58,598,923	NACC1, ZNF321P, 2443 more genes
nsv3903203	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr19: 260,912-59,097,160 , GRCh38.p12 chr19: 260,912-58,585,793	NACC1, BABAM1, 2426 more genes
nsv3903092	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr19: 260,912-58,956,888 , GRCh38.p12 chr19: 260,912-58,445,521	NACC1, LENG8, 2408 more genes
nsv3913730	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr19: 11,199,618-49,821,491 , GRCh37 chr19: 11,338,618-45,129,651 , GRCh38 chr19: 11,227,942-44,626,354	NACC1, BCKDHA, 1102 more genes
nsv3898900	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr19: 9,678,768-14,853,426 , GRCh38.p12 chr19: 9,568,092-14,742,614	NACC1, FBXL12, 253 more genes
nsv3923415	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr19: 10,286,934-14,020,806 , GRCh37 chr19: 10,425,934-14,159,806 , GRCh38 chr19: 10,315,258-14,048,994	NACC1, MAN2B1, 182 more genes
nsv3915094	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr19: 12,132,052-14,751,798 , NCBI36 chr19: 12,103,867-14,723,610 , GRCh37 chr19: 12,242,867-14,862,610	NACC1, RN7SL619P, 123 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 30

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Number of Variants: 20

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Supplemental Content

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