cnn3[All Fields] AND 1[has_clinical] - dbVar - NCBI

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Items: 11

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Number of Variants: 11

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv6313675	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 95,046,805-114,714,931 , GRCh38.p12 chr1: 94,581,249-114,172,309	CNN3, LINC01307, 320 more genes
nsv5673257	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 94,458,793-95,538,454 , GRCh38.p12 chr1: 93,993,237-95,072,898	CNN3, ABCD3, 19 more genes
nsv3877365	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 47,851-249,228,449 , GRCh38.p12 chr1: 47,851-248,934,250	CNN3, MARK1, 4930 more genes
nsv3885206	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 82,154-249,218,992 , GRCh38.p12 chr1: 82,154-248,924,793	CNN3, SNAP47, 4927 more genes
nsv3884414	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr1: 849,467-249,224,684 , GRCh38.p12 chr1: 914,087-248,930,485	CNN3, RNU1-153P, 4887 more genes
nsv3882464	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 93,837,992-121,343,783 , GRCh38.p12 chr1: 93,372,435-121,601,985	CNN3, LINC02607, 513 more genes
nsv3898327	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr1: 83,457,325-104,273,917 , GRCh37 chr1: 83,923,008-104,816,539 , NCBI36 chr1: 83,695,596-104,618,062	CNN3, LINC01773, 322 more genes
nsv3884558	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 94,054,724-111,671,707 , GRCh38.p12 chr1: 93,589,167-111,129,085	CNN3, SLC25A24, 265 more genes
nsv3870933	copy number variation	1	nstd102	human	Benign	GRCh37 chr1: 95,207,442-95,446,903 , GRCh38.p12 chr1: 94,741,886-94,981,347	CNN3, SLC44A3, 4 more genes
nsv4674663	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr1: 93,863,518-96,108,930 , GRCh38.p12 chr1: 93,397,961-95,643,374	CNN3, SLC44A3-AS1, 48 more genes
nsv4436181	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr1: 10,333,430-103,467,088 , GRCh38.p12 chr1: 10,273,372-103,001,532	CNN3, LINC01776, 1853 more genes

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