MS15218 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
nsv890816	copy number variation	21	nstd71	human		NCBI36 chr8: 39,421,344-39,497,557 , GRCh37.p13 chr8: 39,302,187-39,378,400 , GRCh38.p12 chr8: 39,444,668-39,520,881	ADAM3A
nsv880566	copy number variation	1	nstd71	human		NCBI36 chr4: 166,958,578-167,067,451 , GRCh37.p13 chr4: 166,739,128-166,848,001 , GRCh38.p12 chr4: 165,817,976-165,926,849	LOC105377521, TLL1
nsv911765	copy number variation	1	nstd71	human		NCBI36 chr19: 46,141,443-46,195,917 , GRCh37.p13 chr19: 41,449,603-41,504,077 , GRCh38.p12 chr19: 40,943,698-40,998,172	CYP2B7P, CYP2B6
nsv887075	copy number variation	152	nstd71	human		NCBI36 chr7: 136,005-176,320 , GRCh37.p13 chr7: 40,922-81,237 , GRCh38.p12 chr7: 43,902-81,237 , GRCh38.p12 chr7\|NT_187558.1: 1-37,336 , GRCh38.p12 chr7\|NT_187653.1: 36,223-73,558	LOC101929756, LOC105375113
nsv879323	copy number variation	137	nstd71	human		NCBI36 chr4: 69,087,412-69,179,871 , GRCh37.p13 chr4: 69,404,817-69,497,276 , GRCh38.p12 chr4: 68,539,099-68,631,558	LOC100422402, LOC100132651, 2 more genes
nsv889842	copy number variation	2	nstd71	human		NCBI36 chr8: 2,275,525-2,334,306 , GRCh37.p13 chr8\|NW_003571042.1: 322,729-456,870 , GRCh37.p13 chr8: 2,292,235-2,337,777 , GRCh38.p12 chr8: 2,244,437-2,375,564 , GRCh38.p12 chr8\|NT_187576.1: 523,328-657,469	, LOC105377783, 1 more genes
nsv896955	copy number variation	127	nstd71	human		NCBI36 chr11: 5,828,407-5,911,385 , GRCh37.p13 chr11: 5,871,831-5,954,809 , GRCh38.p12 chr11: 5,850,601-5,933,579	OR52E7P, OR52E4, 4 more genes
nsv883617	copy number variation	1	nstd71	human		NCBI36 chr6: 29,963,685-29,986,717 , GRCh37.p13 chr6\|NT_167246.1: 1,157,859-1,172,914 , GRCh37.p13 chr6: 29,855,706-29,878,738 , GRCh38.p12 chr6\|NT_167246.2: 1,152,239-1,167,294 , GRCh38.p12 chr6: 29,887,929-29,910,961	HLA-A, HLA-T, 4 more genes
nsv890119	copy number variation	1	nstd71	human		NCBI36 chr8: 7,184,351-7,947,780 , GRCh37.p13 chr8: 7,196,941-7,910,370 , GRCh38.p12 chr8: 7,339,419-8,052,848	LOC105377801, USP17L3, 55 more genes
nsv889709	copy number variation	1	nstd71	human		NCBI36 chr8: 1,569,246-2,200,350 , GRCh37.p13 chr8: 1,581,839-1,965,389 , GRCh38.p12 chr8: 1,633,673-2,017,223	LOC105377779, DLGAP2, 11 more genes
nsv901296	copy number variation	150	nstd71	human		NCBI36 chr14: 19,261,709-19,494,891 , GRCh37.p13 chr14: 20,191,869-20,425,051 , GRCh38.p12 chr14: 19,723,710-19,956,892	OR4K16P, OR4K2, 12 more genes

Supplemental Content

Filters: Manage Filters

Find related data

Search details

Recent activity

Clear Turn Off Turn On

MS15218 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)