MS14416 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
nsv875419	copy number variation	1	nstd71	human		NCBI36 chr2: 173,962,676-174,005,905 , GRCh37.p13 chr2: 174,254,430-174,297,659 , GRCh38.p12 chr2: 173,389,702-173,432,931	JPT1P1
nsv889263	copy number variation	249	nstd71	human		NCBI36 chr7: 141,410,335-141,441,259 , GRCh37.p13 chr7\|NW_003571040.1: 206,017-236,941 , GRCh37.p13 chr7: 141,763,866-141,794,790 , GRCh38.p12 chr7: 142,064,066-142,094,990 , GRCh38.p12 chr7\|NT_187562.1: 25,946-56,870	MGAM
nsv892542	copy number variation	7	nstd71	human		NCBI36 chr9: 12,083,072-12,110,085 , GRCh37.p13 chr9: 12,093,072-12,120,085 , GRCh38.p12 chr9: 12,093,072-12,120,085	LOC105375976
nsv885023	copy number variation	16	nstd71	human		NCBI36 chr6: 32,604,890-32,615,216 , GRCh37.p13 chr6: 32,496,912-32,507,238 , GRCh38.p12 chr6: 32,529,135-32,539,461 , GRCh38.p12 chr6\|NT_167249.2: 3,833,381-3,839,512 , GRCh38.p12 chr6\|NT_167247.2: 3,858,983-3,865,114	HLA-DRB5
nsv894824	copy number variation	4	nstd71	human		NCBI36 chr10: 6,253,986-6,268,232 , GRCh37.p13 chr10: 6,213,980-6,228,226 , GRCh38.p12 chr10: 6,172,017-6,186,263	PFKFB3
nsv879310	copy number variation	1929	nstd71	human		NCBI36 chr4: 69,076,346-69,179,871 , GRCh37.p13 chr4: 69,393,751-69,497,276 , GRCh38.p12 chr4: 68,528,033-68,631,558	LOC100422402, LOC100132651, 2 more genes
nsv873055	copy number variation	31	nstd71	human		NCBI36 chr1: 195,087,039-195,199,868 , GRCh37.p13 chr1: 196,820,416-196,933,245 , GRCh38.p12 chr1: 196,851,286-196,964,115	LOC105371675, LOC100996886, 2 more genes
nsv911833	copy number variation	12	nstd71	human		NCBI36 chr19: 47,982,103-48,235,556 , GRCh37.p13 chr19: 43,290,263-43,543,716 , GRCh38.p12 chr19: 42,786,111-43,039,564	PSG8-AS1, CEACAMP8, 7 more genes
nsv884258	copy number variation	146	nstd71	human		NCBI36 chr6: 31,388,306-31,398,785 , GRCh37.p13 chr6\|NT_167249.1: 2,614,037-2,624,528 , GRCh37.p13 chr6: 31,280,327-31,290,806 , GRCh38.p12 chr6: 31,312,550-31,323,029 , GRCh38.p12 chr6\|NT_167249.2: 2,614,739-2,625,230	0
nsv874498	copy number variation	5	nstd71	human		NCBI36 chr2: 87,196,423-87,364,379 , GRCh37.p13 chr2: 87,342,912-87,510,868 , GRCh38.p12 chr2: 87,115,789-87,283,745	LOC102724642, , 6 more genes
nsv903224	copy number variation	61	nstd71	human		NCBI36 chr15: 19,635,853-19,981,763 , GRCh37.p13 chr15: 21,371,194-22,480,399 , GRCh38.p12 chr15: 21,165,865-22,192,448	, POTEB3, 51 more genes

Supplemental Content

Filters: Manage Filters

Find related data

Search details

Recent activity

Clear Turn Off Turn On

MS14416 AND nstd71 (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)