OSC8763 AND nstd224 - dbVar - NCBI

Warning: The NCBI web site requires JavaScript to function. more...

Search results

Items: 11

loading data ...

Number of Variants: 11

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv6620527	copy number variation	1	nstd224	human		GRCh37 chr10: 68,348,941-68,364,342 , GRCh38.p12 chr10: 66,589,183-66,604,584	CTNNA3
nsv6632664	copy number variation	1	nstd224	human		GRCh37 chr8: 12,745,732-12,802,833 , GRCh38.p12 chr8: 12,888,223-12,945,324 , GRCh38.p12 chr8\|NW_018654717.1: 6,083,579-6,140,745	TRMT9B, LOC105379289
nsv6625085	copy number variation	34	nstd224	human		GRCh37 chr1: 110,220,086-110,241,385 , GRCh38.p12 chr1: 109,677,464-109,698,763	GSTM1, GSTM2
nsv6620171	copy number variation	1	nstd224	human		GRCh37 chr10: 123,609,009-123,779,171 , GRCh38.p12 chr10: 121,849,494-122,019,656	ATE1, ATE1-AS1, 2 more genes
nsv6625915	copy number variation	1	nstd224	human		GRCh37 chr1: 169,256,570-169,377,123 , GRCh38.p12 chr1: 169,287,332-169,407,885	BLZF1, NME7, 1 more genes
nsv6624685	copy number variation	256	nstd224	human		GRCh37 chr19: 20,605,360-20,700,135 , GRCh38.p12 chr19: 20,422,554-20,517,329	BNIP3P23, LOC105372317, 2 more genes
nsv6629953	copy number variation	2	nstd224	human		GRCh37 chr4: 69,401,172-69,513,989 , GRCh38.p12 chr4: 68,535,454-68,648,271	UGT2B15, LOC100422402, 3 more genes
nsv6624231	copy number variation	76	nstd224	human		GRCh37 chr17: 34,438,753-34,476,927 , GRCh38.p12 chr17: 36,111,360-36,149,545 , GRCh38.p12 chr17\|NT_187661.1: 65,457-103,642 , GRCh38.p12 chr17\|NT_187614.1: 346,281-384,455	LOC107985055, LOC101927369, 1 more genes
nsv6627198	copy number variation	6	nstd224	human		GRCh37 chr22: 24,302,601-24,385,622 , GRCh38.p12 chr22: 23,960,414-24,002,279 , GRCh38.p12 chr22\|NT_187633.1: 196,776-279,797	DDT, GSTT4, 10 more genes
nsv6625875	copy number variation	1	nstd224	human		GRCh37 chr1: 169,547,458-170,642,899 , GRCh38.p12 chr1: 169,578,220-170,673,758	SELP, GORAB, 23 more genes
nsv6624783	copy number variation	32	nstd224	human		GRCh37 chr19: 53,522,100-53,542,566 , GRCh38.p12 chr19: 53,018,847-53,039,313	0

Supplemental Content

Filters: Manage Filters

Find related data

Search details

Recent activity

Clear Turn Off Turn On

OSC8763 AND nstd224 (12)
dbVar

Your browsing activity is empty.

Activity recording is turned off.

Turn recording back on

See more...

You are here: NCBI > Variation > Database of Genomic Structural Variation (dbVar)