pelo[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
nsv3882037	copy number variation	1	nstd102	human	Benign	GRCh37 chr5: 51,972,277-52,091,647 , GRCh38.p12 chr5: 52,676,443-52,795,813	PELO, ITGA1
nsv3889848	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 17,628,741-176,575,720 , GRCh38.p12 chr5: 17,628,632-177,148,719	PELO, MEGF10, 2080 more genes
nsv3923429	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 49,584,189-62,445,597 , NCBI36 chr5: 49,619,946-62,481,353 , GRCh38 chr5: 50,288,355-63,149,770	PELO, ISCA1P1, 163 more genes
nsv3922909	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr5: 50,462,100-55,862,985 , GRCh37 chr5: 49,757,934-55,158,813 , NCBI36 chr5: 49,793,691-55,194,570	PELO, HMGB1P47, 72 more genes
nsv4728831	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 49,430,268-53,182,665 , GRCh38.p12 chr5: 50,134,434-53,886,835	PELO, LOC107986380, 34 more genes
nsv3886374	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 13,648-180,905,029 , GRCh38.p12 chr5: 13,648-181,478,028	PELO, LOC105374618, 2499 more genes
nsv3871533	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 25,328-180,693,344 , GRCh38.p12 chr5: 25,329-181,266,343	PELO, PCDHGC5, 2492 more genes
nsv3875235	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr5: 113,577-180,719,789 , GRCh38.p12 chr5: 113,462-181,292,788	PELO, SPEF2, 2490 more genes
nsv3911585	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr5: 75,149-73,744,306 , GRCh38 chr5: 22,149-74,412,725 , GRCh37 chr5: 22,149-73,708,550	PELO, LINC02241, 878 more genes
nsv3920391	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr5: 35,201,559-61,903,141 , GRCh37 chr5: 35,201,661-61,198,968 , NCBI36 chr5: 35,237,418-61,234,725	PELO, KRT18P56, 290 more genes
nsv4436202	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr5: 14,685,137-149,511,942 , GRCh38.p12 chr5: 14,685,028-150,132,379	PELO, RNU1-150P, 1757 more genes
nsv3874099	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr5: 50,824,656-53,452,371 , GRCh38.p12 chr5: 51,528,822-54,156,541	PELO, ASS1P9, 25 more genes
nsv3912593	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr5: 332,389-180,837,866 , GRCh37.p13 chr5: 279,389-180,905,260 , GRCh38.p12 chr5: 279,274-181,478,259	PELO, LOC105378993, 2492 more genes
nsv3913817	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr5: 45,566,963-55,802,320 , GRCh38 chr5: 45,566,861-56,506,493 , NCBI36 chr5: 45,602,720-55,838,077	PELO, LINC02118, 90 more genes
nsv4456673	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr5: 52,053,923-52,680,028 , GRCh38.p12 chr5: 52,758,089-53,384,198	PELO, ITGA2, 8 more genes

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