rwdd3[All Fields] AND 1[has_clinical] - dbVar - NCBI

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Items: 14

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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
nsv4674374	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr1: 95,638,426-95,750,723 , GRCh38.p12 chr1: 95,172,870-95,285,167	RWDD3, TLCD4, 2 more genes
nsv3906758	copy number variation	1	nstd102	human	Uncertain significance	GRCh38 chr1: 95,230,768-95,286,879 , GRCh37 chr1: 95,696,324-95,752,435 , NCBI36 chr1: 95,468,912-95,525,023	RWDD3, TLCD4-RWDD3, 1 more genes
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	RWDD3, LINC01307, 320 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	RWDD3, 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	RWDD3, 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	RWDD3, 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	RWDD3, 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	RWDD3, 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	RWDD3, SLC25A24, 265 more genes
nsv3876197	copy number variation	1	nstd102	human	Benign	GRCh37 chr1: 95,656,619-95,782,533 , GRCh38.p12 chr1: 95,191,063-95,316,977	RWDD3, TLCD4-RWDD3, 5 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	RWDD3, CNN3, 48 more genes
nsv3917410	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr1: 95,368,888-95,608,620 , GRCh37.p13 chr1: 95,596,300-95,836,032 , GRCh38.p12 chr1: 95,130,744-95,370,476	RWDD3, LOC107985420, 7 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	RWDD3, LINC01776, 1853 more genes
nsv3882833	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr1: 95,554,116-96,359,492 , GRCh38.p12 chr1: 95,088,560-95,893,936	RWDD3, LINC02607, 10 more genes

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rwdd3[All Fields] AND 1[has_clinical] (15)
dbVar
chst14 [Perca flavescens]
chst14 [Perca flavescens]
Gene ID:114562009

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