nog2[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
nsv3871174	copy number variation	1	nstd102	human	Benign	GRCh37 chr1: 38,031,972-38,105,212 , GRCh38.p12 chr1: 37,566,371-37,639,540	DNALI1, GNL2, 1 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	MARK1, LINC02766, 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	SNAP47, STK40, 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	RNU1-153P, MIR3917, 4887 more genes
nsv3901163	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 24,707,696-41,886,350 , GRCh38 chr1: 24,381,206-41,401,517 , NCBI36 chr1: 24,580,283-41,658,937	TMEM222, ZBTB8OS, 453 more genes
nsv6313688	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 33,285,582-47,891,811 , GRCh38.p12 chr1: 32,819,981-47,426,139	LOC107984940, PPIAP36, 407 more genes
nsv3886123	copy number variation	1	nstd102	human	Likely benign	GRCh37 chr1: 37,766,562-38,727,114 , GRCh38.p12 chr1: 37,300,961-38,261,442	FHL3, DNALI1, 36 more genes
nsv3883497	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr1: 38,001,813-38,068,791 , GRCh38.p12 chr1: 37,536,212-37,603,190	DNALI1, SNIP1, 4 more genes
nsv3871383	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr1: 38,001,813-38,043,237 , GRCh38.p12 chr1: 37,536,212-37,577,636	DNALI1, GNL2, 4 more genes
nsv6313765	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr1: 36,041,366-39,112,237 , GRCh38.p12 chr1: 35,575,765-38,646,565	RNU6-510P, AGO3, 78 more genes
nsv3873946	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr1: 38,005,705-38,077,489 , GRCh38.p12 chr1: 37,540,104-37,611,817	RPS27P9, FTH1P1, 5 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	LINC01776, IGSF21-AS1, 1853 more genes
nsv3878135	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr1: 33,241,563-46,663,513 , GRCh38.p12 chr1: 32,775,962-46,197,841	LINC02786, LOC105378678, 365 more genes
nsv7095992	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr1: 38,003,349-38,273,852 , GRCh38.p12 chr1: 37,537,748-37,808,180	LOC105378650, ACTN4P2, 15 more genes

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nog2[All Fields] AND 1[has_clinical] (15)
dbVar
Conserved Domain Links for Protein (Select 1777972342) (1)
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