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

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Items: 15

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Number of Variants: 15

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv4346788	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 32,859,415-36,454,915 , GRCh38.p12 chr1: 32,393,814-35,989,314	CLSPN, LOC100419802, 75 more genes
nsv6636592	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 35,104,233-37,357,913 , GRCh38.p12 chr1: 34,638,632-36,892,312	CLSPN, EFCAB14P1, 56 more genes
nsv3883608	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 34,830,287-36,945,093 , GRCh38.p12 chr1: 34,364,686-36,479,492	CLSPN, LSM10, 52 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	CLSPN, 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	CLSPN, 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	CLSPN, RNU1-153P, 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	CLSPN, TMEM222, 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	CLSPN, LOC107984940, 407 more genes
nsv3874782	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 31,562,164-37,421,958 , GRCh38.p12 chr1: 31,089,317-36,956,357	CLSPN, LOC101929444, 143 more genes
nsv3890386	copy number variation	1	nstd102	human	Likely pathogenic	NCBI36 chr1: 34,992,126-36,293,498 , GRCh37 chr1: 35,219,539-36,520,911 , GRCh38 chr1: 34,753,938-36,055,310	CLSPN, GJA4, 31 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	CLSPN, RNU6-510P, 78 more genes
nsv3882463	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr1: 35,950,860-36,465,764 , GRCh38.p12 chr1: 35,485,259-36,000,163	CLSPN, PSMB2, 10 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	CLSPN, LINC01776, 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	CLSPN, LINC02786, 365 more genes
nsv6313478	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr1: 35,950,860-36,635,695 , GRCh38.p12 chr1: 35,485,259-36,170,094	CLSPN, LOC100128093, 17 more genes

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