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

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Items: 13

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Number of Variants: 13

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv3902804	copy number variation	1	nstd102	human	Likely benign	GRCh38 chr1: 51,814,691-51,941,708 , GRCh37 chr1: 52,280,363-52,407,380 , NCBI36 chr1: 52,052,951-52,179,968	NRDC, TSEN15P2, 2 more genes
nsv3874555	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr1: 52,192,823-52,364,203 , GRCh38.p12 chr1: 51,727,151-51,898,531	NRDC, OSBPL9, 2 more genes
nsv4674547	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 47,272,184-52,505,405 , GRCh38.p12 chr1: 46,806,512-52,039,733	NRDC, RAB3B, 90 more genes
nsv5381135	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 51,941,877-56,688,514 , GRCh38.p12 chr1: 51,476,205-56,222,842	NRDC, LRP8-DT, 122 more genes
nsv3871136	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 51,729,573-55,164,001 , GRCh38.p12 chr1: 51,263,901-54,698,328	NRDC, MROH7, 100 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	NRDC, 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	NRDC, 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	NRDC, RNU1-153P, 4887 more genes
nsv6638064	copy number variation	1	nstd102	human	association	GRCh38 chr1: 48,666,286-52,808,894 , GRCh37.p13 chr1: 49,131,958-53,274,566	NRDC, LOC105378710, 80 more genes
nsv6290622	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr1: 51,850,394-52,256,345 , GRCh38.p12 chr1: 51,384,722-51,790,673	NRDC, GAPDHP51, 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	NRDC, LINC01776, 1853 more genes
nsv6313756	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr1: 51,755,130-52,521,150 , GRCh38.p12 chr1: 51,289,458-52,055,478	NRDC, EPS15, 21 more genes
nsv6636580	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr1: 51,797,643-52,256,345 , GRCh38.p12 chr1: 51,331,971-51,790,673	NRDC, RNU6-877P, 10 more genes

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