SP52713 AND nstd71 - 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
nsv884822	copy number variation	2547	nstd71	human		NCBI36 chr6: 32,560,168-32,593,470 , GRCh37.p13 chr6: 32,452,190-32,485,492 , GRCh38.p12 chr6: 32,484,413-32,517,715	HLA-DRB5
nsv911763	copy number variation	10	nstd71	human		NCBI36 chr19: 46,134,005-46,207,542 , GRCh37.p13 chr19: 41,442,165-41,515,702 , GRCh38.p12 chr19: 40,936,260-41,009,797	CYP2B7P, CYP2B6
nsv874634	copy number variation	114	nstd71	human		NCBI36 chr2: 89,721,421-89,911,010 , GRCh37.p13 chr2: 90,084,116-90,273,705 , GRCh38.p12 chr2: 90,045,284-90,234,838	IGKV3D-15, IGKV1D-16, 14 more genes
nsv872399	copy number variation	1	nstd71	human		NCBI36 chr1: 147,710,728-147,825,852 , GRCh37.p13 chr1: 149,444,104-149,559,228 , GRCh38.p12 chr: NaN-NaN	0
nsv895270	copy number variation	14	nstd71	human		NCBI36 chr10: 47,013,541-47,197,303 , GRCh37.p13 chr10: 47,543,535-47,689,665 , GRCh37.p13 chr10\|NW_003871068.1: 443,414-589,544 , GRCh38.p12 chr10: 46,172,299-46,356,071	ANTXRL, AGAP14P, 3 more genes
nsv876979	copy number variation	3	nstd71	human		NCBI36 chr3: 75,520,579-75,654,889 , GRCh37.p13 chr3: 75,437,889-75,572,199 , GRCh38.p12 chr3: 75,388,738-75,523,048	ALG1L6P, ENPP7P2, 4 more genes
nsv905755	copy number variation	2	nstd71	human		NCBI36 chr16: 31,466,721-31,541,722 , GRCh37.p13 chr16: 31,559,220-31,634,221 , GRCh38.p12 chr16: 31,547,899-31,622,900	VN1R64P, LINC02190, 4 more genes
nsv903247	copy number variation	118	nstd71	human		NCBI36 chr15: 19,635,853-20,203,694 , GRCh37.p13 chr15: 21,371,194-22,652,330 , GRCh38.p12 chr15: 21,165,865-22,308,242	OR11J6P, LOC642131, 56 more genes
nsv901294	copy number variation	38	nstd71	human		NCBI36 chr14: 19,261,709-19,493,705 , GRCh37.p13 chr14: 20,191,869-20,423,865 , GRCh38.p12 chr14: 19,723,710-19,955,706	OR4K5, OR4Q3, 12 more genes
nsv890285	copy number variation	9	nstd71	human		NCBI36 chr8: 7,683,445-7,840,086 , GRCh37.p13 chr8: 7,646,035-7,802,676 , GRCh38.p12 chr8: 7,788,513-7,945,154 , GRCh38.p12 chr8\|NW_018654717.1: 5,385,730-5,513,617	DEFB104B, DEFB106B, 18 more genes
nsv915208	copy number variation	1	nstd71	human		NCBI36 chr22: 21,059,244-21,115,308 , GRCh37.p13 chr22: 22,729,244-22,785,308 , GRCh38.p12 chr22\|NT_187629.1: 1,428-66,609 , GRCh38.p12 chr22: 22,374,876-22,430,970	LOC105379604, IGLV1-36, 17 more genes

Supplemental Content

Filters: Manage Filters

Find related data

Search details

Recent activity

Clear Turn Off Turn On

SP52713 AND nstd71 (12)
dbVar
Homologene neighbors for GEO Profiles (Select 113463360) (0)
GEO Profiles

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)