ppwd1[All Fields] AND 1[has_clinical] - dbVar - NCBI

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Number of Variants: 17

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
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	PPWD1, MEGF10, 2080 more genes
nsv6313676	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 64,049,692-70,306,646 , GRCh38.p12 chr5: 64,753,865-71,010,819	PPWD1, BCL9P1, 105 more genes
nsv3921568	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 64,228,590-68,791,331 , NCBI36 chr5: 64,264,346-68,827,087 , GRCh38 chr5: 64,932,763-69,495,504	PPWD1, LOC100419549, 67 more genes
nsv6312114	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 63,256,278-65,374,358 , GRCh38.p12 chr5: 63,960,451-66,078,530	PPWD1, RNF180, 23 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	PPWD1, 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	PPWD1, 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	PPWD1, 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	PPWD1, LINC02241, 878 more genes
nsv4578696	copy number variation	1	nstd102	human	Likely pathogenic	GRCh38 chr5: 58,780,641-73,523,380 , GRCh37.p13 chr5: 58,076,468-72,819,205	PPWD1, TRIM23, 215 more genes
nsv3916577	copy number variation	1	nstd102	human	Likely pathogenic	NCBI36 chr5: 64,745,346-65,762,306 , GRCh37 chr5: 64,709,590-65,726,550 , GRCh38 chr5: 65,413,763-66,430,722	PPWD1, TRIM23, 15 more genes
nsv3883692	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr5: 58,966,132-68,847,066 , GRCh38.p12 chr5: 59,670,306-69,551,239	PPWD1, TRIM23, 125 more genes
nsv3920421	copy number variation	1	nstd102	human	Likely pathogenic	NCBI36 chr5: 62,538,695-70,622,774 , GRCh37 chr5: 62,502,939-70,587,018 , GRCh38 chr5: 63,207,112-71,291,191	PPWD1, TRIM23, 124 more genes
nsv3910901	copy number variation	1	nstd102	human	Likely benign	GRCh38 chr5: 65,162,063-65,680,676 , NCBI36 chr5: 64,493,646-65,012,259 , GRCh37 chr5: 64,457,890-64,976,503	PPWD1, RPS2P23, 9 more genes
nsv4675585	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr5: 64,775,928-64,994,289 , GRCh38.p12 chr5: 65,480,101-65,698,462	PPWD1, ADAMTS6, 6 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	PPWD1, RNU1-150P, 1757 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	PPWD1, LOC105378993, 2492 more genes
nsv3916989	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr5: 64,543,311-66,078,345 , GRCh37 chr5: 64,507,555-66,042,589 , GRCh38 chr5: 65,211,728-66,746,761	PPWD1, LINC02229, 20 more genes

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