cnn1[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
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	CNN1, SWSAP1, 164 more genes
nsv3922999	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr19: 10,240,071-12,946,266 , GRCh37.p13 chr19: 10,379,071-13,085,266 , GRCh38.p12 chr19: 10,268,395-12,974,452	CNN1, ZNF433, 155 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	CNN1, JUNB, 135 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	CNN1, ZNF763, 105 more genes
nsv4729806	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr19: 10,957,601-11,672,041 , GRCh38.p12 chr19: 10,846,925-11,561,226	CNN1, DOCK6-AS1, 32 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	CNN1, 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	CNN1, 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	CNN1, 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	CNN1, 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	CNN1, 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	CNN1, MAN2B1, 182 more genes
nsv3920616	copy number variation	1	nstd102	human	Likely pathogenic	NCBI36 chr19: 8,802,823-13,303,041 , GRCh37 chr19: 8,941,823-13,442,041 , GRCh38 chr19: 8,831,147-13,331,227	CNN1, ACP5, 236 more genes
nsv4685775	copy number variation	1	nstd102	human	not provided	GRCh37 chr19: 10,642,984-12,810,067 , GRCh38.p12 chr19: 10,532,308-12,699,253	CNN1, SLC44A2, 114 more genes
nsv4451686	copy number variation	1	nstd102	human	not provided	GRCh37 chr19: 10,642,984-12,810,067 , GRCh38.p12 chr19: 10,532,308-12,699,253	CNN1, ODAD3, 114 more genes
nsv3899944	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr19: 11,608,072-14,543,046 , GRCh38.p12 chr19: 11,497,257-14,432,234	CNN1, RNA5SP465, 145 more genes
nsv7095458	copy number variation	4	nstd102	human	Uncertain significance	GRCh37 chr19: 10,828,919-13,482,613 , GRCh38.p12 chr19: 10,718,243-13,371,799	CNN1, WDR83OS, 140 more genes
nsv7095400	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr19: 11,277,234-13,249,220 , GRCh38.p12 chr19: 11,166,558-13,138,406	CNN1, ZNF627, 120 more genes
nsv6291543	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr19: 9,941,033-11,739,567 , GRCh38.p12 chr19: 9,830,357-11,628,752	CNN1, KRI1, 88 more genes
nsv4676222	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr19: 11,445,773-12,160,664 , GRCh38.p12 chr19: 11,335,097-12,049,849	CNN1, ECSIT, 41 more genes
nsv3915706	copy number variation	1	nstd102	human	Uncertain significance	GRCh38 chr19: 11,138,895-11,549,951 , NCBI36 chr19: 11,110,571-11,521,766 , GRCh37 chr19: 11,249,571-11,660,766	CNN1, ELAVL3, 22 more genes

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Items: 20

Number of Variants: 20

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