pepd[All Fields] AND 1[has_clinical] - dbVar

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Number of Variants: 20

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv4457510	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr19: 33,963,521-33,975,799 , GRCh38.p12 chr19: 33,472,615-33,484,893	PEPD
nsv6310627	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr19: 33,902,558-33,904,569 , GRCh38.p12 chr19: 33,411,652-33,413,663	PEPD
nsv3872945	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr19: 33,387,843-33,388,624 , GRCh37 chr19: 33,878,749-33,879,530	PEPD
nsv6310683	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr19: 33,968,932-33,969,016 , GRCh38.p12 chr19: 33,478,026-33,478,110	PEPD
nsv4457819	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr19: 33,842,279-33,986,911 , GRCh38.p12 chr19: 33,351,373-33,496,005	PEPD, AKR1B1P7, 1 more genes
nsv3919296	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr19: 34,844,605-43,297,203 , GRCh37 chr19: 30,152,765-38,605,363 , GRCh38 chr19: 29,661,858-38,114,723	PEPD, UBA2, 241 more genes
nsv3916007	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr19: 30,162,231-38,393,630 , NCBI36 chr19: 34,854,071-43,085,470 , GRCh38 chr19: 29,671,324-37,902,990	PEPD, MAG, 238 more genes
nsv3918197	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr19: 31,367,353-35,417,098 , NCBI36 chr19: 36,550,099-40,599,840 , GRCh37 chr19: 31,858,259-35,908,000	PEPD, LINC01531, 110 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	PEPD, 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	PEPD, 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	PEPD, LENG8, 2408 more genes
nsv3913730	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr19: 11,199,618-49,821,491 , GRCh37 chr19: 11,338,618-45,129,651 , GRCh38 chr19: 11,227,942-44,626,354	PEPD, BCKDHA, 1102 more genes
nsv6290300	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr19: 19,546,923-41,313,229 , GRCh38.p12 chr19: 19,436,114-40,807,324	PEPD, ZNF420, 574 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	PEPD, ZNF461, 735 more genes
nsv3914228	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr19: 17,148,576-40,106,894 , GRCh38 chr19: 17,176,767-34,924,150 , GRCh37 chr19: 17,287,576-35,415,054	PEPD, LOC105372355, 411 more genes
nsv3900139	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr19: 30,735,448-36,120,396 , GRCh38.p12 chr19: 30,244,541-35,629,494	PEPD, ZNF599, 130 more genes
nsv3892235	copy number variation	1	nstd102	human	Likely benign	GRCh37 chr19: 33,762,256-34,353,184 , GRCh38.p12 chr19: 33,271,350-33,862,279	PEPD, CEBPA, 9 more genes
nsv3919618	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr19: 32,962,986-39,966,686 , GRCh38 chr19: 27,780,238-34,783,942 , GRCh37 chr19: 28,271,146-35,274,846	PEPD, LINC00906, 112 more genes
nsv7095478	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr19: 33,167,170-36,643,309 , GRCh38.p12 chr19: 32,676,264-36,152,407	PEPD, NFKBID, 141 more genes
nsv6314074	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr19: 32,827,535-35,263,640 , GRCh38.p12 chr19: 32,336,629-34,772,735	PEPD, LOC100130632, 59 more genes

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Items: 20

Number of Variants: 20

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