MS20632 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
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
nsv909839	copy number variation	966	nstd71	human		NCBI36 chr18: 64,895,268-64,909,808 , GRCh37.p13 chr18: 66,744,288-66,758,828 , GRCh38.p12 chr18: 69,077,051-69,091,591	CCDC102B
nsv874272	copy number variation	22	nstd71	human		NCBI36 chr2: 73,700,532-73,767,527 , GRCh37.p13 chr2: 73,847,024-73,914,019 , GRCh38.p12 chr2: 73,619,897-73,686,892	ALMS1P1, NAT8
nsv876465	copy number variation	1	nstd71	human		NCBI36 chr3: 4,420,708-4,461,303 , GRCh37.p13 chr3: 4,445,708-4,486,303 , GRCh38.p12 chr3: 4,404,024-4,444,619	SUMF1, MRPS10P2
nsv911382	copy number variation	222	nstd71	human		NCBI36 chr19: 20,413,668-20,520,617 , GRCh37.p13 chr19: 20,621,828-20,728,777 , GRCh37.p13 chr19\|NW_003571053.2: 356,275-463,224 , GRCh38.p12 chr19: 20,439,022-20,545,971	BNIP3P23, LOC105372317, 2 more genes
nsv879318	copy number variation	371	nstd71	human		NCBI36 chr4: 69,085,989-69,179,871 , GRCh37.p13 chr4: 69,403,394-69,497,276 , GRCh38.p12 chr4: 68,537,676-68,631,558	LOC728807, UGT2B17, 2 more genes
nsv896967	copy number variation	31	nstd71	human		NCBI36 chr11: 5,858,528-5,911,385 , GRCh37.p13 chr11: 5,901,952-5,954,809 , GRCh38.p12 chr11: 5,880,722-5,933,579	LOC112268071, OR52E4, 2 more genes
nsv885540	copy number variation	1	nstd71	human		NCBI36 chr6: 32,708,781-32,743,824 , GRCh37.p13 chr6: 32,600,803-32,635,846 , GRCh37.p13 chr6\|NT_167247.1: 3,939,666-3,970,153 , GRCh37.p13 chr6\|NT_167249.1: 4,034,248-4,064,436 , GRCh37.p13 chr6\|NT_167245.1: 3,882,525-3,914,321 , GRCh38.p12 chr6\|NT_167245.2: 3,876,940-3,908,736 , GRCh38.p12 chr6\|NT_167249.2: 4,034,950-4,065,138 , GRCh38.p12 chr6\|NT_167247.2: 3,934,081-3,964,568 , GRCh38.p12 chr6: 32,633,026-32,668,069	HLA-DQA1, , 4 more genes
nsv889043	copy number variation	56	nstd71	human		NCBI36 chr7: 110,993,130-111,126,464 , GRCh37.p13 chr7: 111,205,894-111,339,228 , GRCh38.p12 chr7: 111,565,838-111,699,172	0
nsv886057	copy number variation	200	nstd71	human		NCBI36 chr6: 67,065,007-67,111,682 , GRCh37.p13 chr6: 67,008,286-67,054,961 , GRCh38.p12 chr6: 66,298,393-66,345,068	0

Supplemental Content

Filters: Manage Filters

Find related data

Search details

Recent activity

Clear Turn Off Turn On

MS20632 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)