OSC5900 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
nsv6632096	copy number variation	1	nstd224	human		GRCh37 chr7: 4,588,632-4,667,201 , GRCh38.p12 chr7: 4,549,001-4,627,570	LOC105375133
nsv6630264	copy number variation	1	nstd224	human		GRCh37 chr5: 108,792,289-108,868,352 , GRCh38.p12 chr5: 109,456,588-109,532,651	LOC105379117
nsv6623881	copy number variation	1	nstd224	human		GRCh37 chr16: 6,807,461-6,864,390 , GRCh38.p12 chr16: 6,757,460-6,814,389	RBFOX1
nsv6629898	copy number variation	832	nstd224	human		GRCh37 chr4: 69,401,172-69,435,811 , GRCh38.p12 chr4: 68,535,454-68,570,093	UGT2B17
nsv6627532	copy number variation	26	nstd224	human		GRCh37 chr2: 194,579,732-194,604,192 , GRCh38.p12 chr2: 193,715,008-193,739,468	SEC61GP1
nsv6621850	copy number variation	39	nstd224	human		GRCh37 chr12: 8,005,624-8,109,412 , GRCh38.p12 chr12: 7,853,028-7,956,816	LOC100130582, RPS20P29, 3 more genes
nsv6630883	copy number variation	34	nstd224	human		GRCh37 chr5: 777,133-816,095 , GRCh38.p12 chr5: 777,018-815,980	ZDHHC11B, ZDHHC11, 1 more genes
nsv6627123	copy number variation	4	nstd224	human		GRCh37 chr22: 42,525,780-42,536,064 , GRCh38.p12 chr22\|NT_187682.1: 52,119-62,403	LOC102723722, CYP2D7, 1 more genes
nsv6627763	copy number variation	1	nstd224	human		GRCh37 chr2: 140,348,800-140,385,381 , GRCh38.p12 chr2: 139,591,231-139,627,812	0
nsv6622363	copy number variation	1	nstd224	human		GRCh37 chr14: 20,202,116-20,416,499 , GRCh38.p12 chr14: 19,733,957-19,948,340	OR4K5, OR4K2, 11 more genes
nsv6629569	copy number variation	48	nstd224	human		GRCh37 chr4: 161,863,893-161,923,192 , GRCh38.p12 chr4: 160,942,741-161,002,040	0

Supplemental Content

Filters: Manage Filters

Find related data

Search details

Recent activity

Clear Turn Off Turn On

OSC5900 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)