rtn2[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
nsv3891669	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr19: 43,013,365-47,241,534 , GRCh38.p12 chr19: 42,509,213-46,738,277	RTN2, MIR320E, 189 more genes
nsv3904885	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr19: 68,029-59,110,290 , GRCh38.p12 chr19: 68,029-58,598,923	RTN2, ZNF321P, 2443 more genes
nsv3903203	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr19: 260,912-59,097,160 , GRCh38.p12 chr19: 260,912-58,585,793	RTN2, BABAM1, 2426 more genes
nsv3903092	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr19: 260,912-58,956,888 , GRCh38.p12 chr19: 260,912-58,445,521	RTN2, LENG8, 2408 more genes
nsv4457372	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr19: 28,271,106-49,213,832 , GRCh38.p12 chr19: 27,780,198-48,710,575	RTN2, ZNF461, 735 more genes
nsv4676357	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr19: 44,738,088-53,621,561 , GRCh38.p12 chr19: 44,233,935-53,118,308	RTN2, MIR4324, 485 more genes
nsv3924836	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr19: 50,166,517-53,452,471 , GRCh37 chr19: 45,474,677-48,760,659 , GRCh38 chr19: 44,971,420-48,257,402	RTN2, IGFL1P1, 145 more genes
nsv3921787	copy number variation	1	nstd102	human	Likely pathogenic	NCBI36 chr19: 50,582,487-52,026,097 , GRCh37 chr19: 45,890,647-47,334,257 , GRCh38 chr19: 45,387,389-46,831,000	RTN2, CALM3, 71 more genes
nsv3924271	copy number variation	1	nstd102	human	Uncertain significance	GRCh38 chr19: 45,481,858-45,710,518 , GRCh37 chr19: 45,985,116-46,213,776 , NCBI36 chr19: 50,676,956-50,905,616	RTN2, RN7SL836P, 15 more genes
nsv4676350	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr19: 45,531,056-48,174,177 , GRCh38.p12 chr19: 45,027,798-47,670,920	RTN2, NKPD1, 112 more genes
nsv6314081	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr19: 45,074,342-46,133,841 , GRCh38.p12 chr19: 44,571,096-45,630,583	RTN2, EXOC3L2, 50 more genes
nsv3921263	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr19: 45,790,514-46,237,336 , NCBI36 chr19: 50,482,354-50,929,176 , GRCh38 chr19: 45,287,256-45,734,078	RTN2, MIR642A, 26 more genes
nsv3899964	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr19: 45,945,375-46,215,558 , GRCh38.p12 chr19: 45,442,117-45,712,300	RTN2, PPM1N, 17 more genes

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