SP50522 AND nstd71 - dbVar - NCBI

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

Search results

Items: 13

loading data ...

Number of Variants: 13

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv878754	copy number variation	1	nstd71	human		NCBI36 chr4: 22,628,668-22,755,985 , GRCh37.p13 chr4: 23,019,570-23,146,887 , GRCh38.p12 chr4: 23,017,947-23,145,264	LOC105374524
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
nsv890754	copy number variation	920	nstd71	human		NCBI36 chr8: 39,350,791-39,509,376 , GRCh37.p13 chr8: 39,231,634-39,390,219 , GRCh38.p12 chr8: 39,374,115-39,532,700	ADAM5, ADAM3A
nsv885195	copy number variation	2	nstd71	human		NCBI36 chr6: 32,615,216-32,633,666 , GRCh37.p13 chr6: 32,507,238-32,525,688 , GRCh38.p12 chr6: 32,539,461-32,557,911	HLA-DRB6, RNU1-61P
nsv905952	copy number variation	17	nstd71	human		NCBI36 chr16: 32,406,646-32,579,320 , GRCh37.p13 chr16: 32,499,145-32,671,819 , GRCh38.p12 chr16: 32,487,824-32,660,498	LOC107984013, FAM153DP
nsv895573	copy number variation	1	nstd71	human		NCBI36 chr10: 65,276,235-65,368,946 , GRCh37.p13 chr10: 65,606,229-65,698,940 , GRCh38.p12 chr10: 63,846,469-63,939,180	LOC101928859, RPL7AP50
nsv907853	copy number variation	28	nstd71	human		NCBI36 chr17: 18,971,335-19,040,640 , GRCh37.p13 chr17: 19,030,610-19,100,047 , GRCh38.p12 chr17: 19,127,297-19,196,734	SNORD3C, GRAPL-AS1, 3 more genes
nsv914684	copy number variation	27	nstd71	human		NCBI36 chr22: 23,991,725-24,113,704 , GRCh37.p13 chr22: 25,661,725-25,783,704 , GRCh38.p12 chr22: 25,265,758-25,387,737	LRP5L, IGLL3P, 2 more genes
nsv873875	copy number variation	3	nstd71	human		NCBI36 chr2: 36,234,999-36,285,895 , GRCh37.p13 chr2: 36,381,495-36,432,391 , GRCh38.p12 chr2: 36,154,352-36,205,248	0
nsv884256	copy number variation	61	nstd71	human		NCBI36 chr6: 31,388,306-31,396,472 , GRCh37.p13 chr6: 31,280,327-31,288,493 , GRCh37.p13 chr6\|NT_167246.1: 2,627,146-2,631,393 , GRCh37.p13 chr6\|NT_167249.1: 2,614,037-2,622,207 , GRCh38.p12 chr6\|NT_167246.2: 2,621,526-2,625,775 , GRCh38.p12 chr6: 31,312,550-31,320,716 , GRCh38.p12 chr6\|NT_167249.2: 2,614,739-2,622,909	0
nsv880191	copy number variation	6	nstd71	human		NCBI36 chr4: 145,012,409-145,259,965 , GRCh37.p13 chr4: 144,792,959-145,040,515 , GRCh38.p12 chr4: 143,871,806-144,119,362	GYPA, GYPE, 6 more genes
nsv874523	copy number variation	4	nstd71	human		NCBI36 chr2: 87,226,520-87,375,788 , GRCh37.p13 chr2: 87,373,009-87,522,277 , GRCh38.p12 chr2: 87,145,886-87,295,154	CENPNP1, LOC102724642, 4 more genes
nsv914929	copy number variation	13	nstd71	human		NCBI36 chr22: 24,215,704-24,244,593 , GRCh37.p13 chr22: 25,885,704-25,914,593 , GRCh38.p12 chr22: 25,489,737-25,518,626	0

Supplemental Content

Filters: Manage Filters

Find related data

Search details

Recent activity

Clear Turn Off Turn On

SP50522 AND nstd71 (14)
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)