dbVar for Gene (Select 202309) - 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
nsv5465476	copy number variation	1	nstd206	human		GRCh38 chr5: 57,931,909-58,692,386 , GRCh37.p13 chr5: 57,227,736-57,988,213	PLK2, RAB3C, 7 more genes
nsv5313375	copy number variation	1	nstd204	human		GRCh37.p13 chr5: 57,227,752-57,988,202 , GRCh38.p13 chr5: 57,931,925-58,692,375	PLK2, RAB3C, 7 more genes
nsv5221686	copy number variation	1	nstd204	human		GRCh38.p13 chr5: 58,390,301-58,563,100 , GRCh37.p13 chr5: 57,686,128-57,858,927	LINC02108, LOC105378984, 3 more genes
nsv5090979	mobile element insertion	1	nstd203	human		GRCh38 chr5: 58,496,486-58,496,492 , GRCh37.p13 chr5: 57,792,313-57,792,319	GAPT
nsv4948789	copy number variation	1	nstd200	human		GRCh38 chr5: 57,931,929-58,692,366 , GRCh37.p13 chr5: 57,227,756-57,988,193	LOC105378984, PLK2, 7 more genes
nsv4523070	copy number variation	1	nstd166	human		GRCh37.p13 chr5: 57,245,997-58,257,000 , GRCh38.p12 chr5: 57,950,170-58,961,173	GAPT, MIR548AE2, 8 more genes
nsv4488849	mobile element insertion	1	nstd166	human		GRCh37.p13 chr5: 57,792,313-57,792,313 , GRCh38.p12 chr5: 58,496,486-58,496,486	GAPT
nsv4456295	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr5: 56,283,070-58,079,028 , GRCh38.p12 chr5: 56,987,243-58,783,201	SALL4P1, LINC02225, 17 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	RNU1-150P, RNU6-727P, 1757 more genes
nsv4119813	copy number variation	1	nstd166	human		GRCh37.p13 chr5: 39,131,458-67,637,618 , GRCh38.p12 chr5: 39,131,356-68,341,790	, ESM1, 305 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	ISCA1P1, LOC643307, 163 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	KRT18P56, LINC01265, 290 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	LOC105378993, LOC107986375, 2492 more genes
nsv3911731	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr5: 56,279,434-61,056,985 , GRCh38 chr5: 56,947,850-61,725,401 , GRCh37 chr5: 56,243,677-61,021,228	MIR548AE2, RNU6-913P, 52 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	LINC02241, ATPSCKMT, 878 more genes
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	MEGF10, LOC100128407, 2080 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	LOC105374618, HARS1, 2499 more genes
nsv3882873	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr5: 56,574,178-58,587,671 , GRCh38.p12 chr5: 57,278,351-59,291,845	RMEL3, LOC105378984, 17 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	SPEF2, NDST1, 2490 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	PCDHGC5, RGS14, 2492 more genes

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Number of Variants: 20

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