SP57593 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
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
nsv880475	copy number variation	143	nstd71	human		NCBI36 chr5: 32,137,157-32,205,304 , GRCh37.p13 chr5: 32,101,400-32,169,547 , GRCh38.p12 chr5: 32,101,294-32,169,441	PDZD2, GOLPH3
nsv908380	copy number variation	142	nstd71	human		NCBI36 chr17: 41,775,690-41,943,845 , GRCh37.p13 chr17: 44,419,932-44,588,529 , GRCh38.p12 chr17: 46,342,566-46,511,163	LRRC37A2, ARL17A, 3 more genes
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
nsv911348	copy number variation	463	nstd71	human		NCBI36 chr19: 20,386,247-20,520,617 , GRCh37.p13 chr19\|NW_003571053.2: 329,860-463,224 , GRCh37.p13 chr19: 20,522,409-20,728,777 , GRCh38.p12 chr19: 20,411,600-20,545,971	BNIP3P23, LOC105372317, 4 more genes
nsv899669	copy number variation	9	nstd71	human		NCBI36 chr12: 130,366,128-130,395,261 , GRCh37.p13 chr12: 131,800,175-131,829,308 , GRCh38.p12 chr12: 131,315,630-131,344,763	0
nsv899006	copy number variation	1	nstd71	human		NCBI36 chr12: 36,821,928-37,137,909 , GRCh37.p13 chr12: 38,535,661-38,851,642 , GRCh38.p12 chr12: 38,141,859-38,457,840	NF1P12, LOC100421618, 5 more genes
nsv908098	copy number variation	9	nstd71	human		NCBI36 chr17: 31,460,645-31,567,477 , GRCh37.p13 chr17: 34,436,532-34,543,364 , GRCh37.p13 chr17\|NW_003315949.1: 1-65,496 , GRCh38.p12 chr17: 36,109,139-36,215,910 , GRCh38.p12 chr17\|NT_187614.1: 344,060-415,644 , GRCh38.p12 chr17\|NT_187661.1: 63,236-134,851	CCL4L2, LOC101927369, 7 more genes
nsv898991	copy number variation	4	nstd71	human		NCBI36 chr12: 36,392,400-36,696,954 , GRCh37.p13 chr12: 38,106,133-38,410,687 , GRCh38.p12 chr12: 37,712,331-38,016,885	0
nsv906406	copy number variation	6	nstd71	human		NCBI36 chr16: 32,469,358-32,489,297 , GRCh37.p13 chr16: 32,561,857-32,581,796 , GRCh38.p12 chr16: 32,550,536-32,570,475	0

Supplemental Content

Filters: Manage Filters

Find related data

Search details

Recent activity

Clear Turn Off Turn On

SP57593 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)