nup160[All Fields] AND 1[has_clinical] - dbVar - NCBI

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

Search results

Items: 19

loading data ...

Number of Variants: 19

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv4675809	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr11: 47,852,329-48,010,053 , GRCh38.p12 chr11: 47,830,777-47,988,501	NUP160, LOC100287189, 2 more genes
nsv5380796	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 11,835,569-118,373,112 , GRCh38.p12 chr11: 11,814,022-118,502,397	NUP160, FAUP4, 2031 more genes
nsv3913842	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 39,200,802-49,157,287 , NCBI36 chr11: 39,157,378-49,113,863 , GRCh38 chr11: 39,179,252-49,135,735	NUP160, MIR3160-1, 162 more genes
nsv3924778	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr11: 41,118,322-48,643,003 , GRCh37 chr11: 41,139,872-48,664,555 , NCBI36 chr11: 41,096,448-48,621,131	NUP160, F2, 140 more genes
nsv3914709	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr11: 46,840,454-48,643,003 , GRCh37 chr11: 46,862,005-48,664,555 , NCBI36 chr11: 46,818,581-48,621,131	NUP160, CELF1, 56 more genes
nsv3893233	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 70,864-134,938,470 , GRCh38.p12 chr11: 70,864-135,068,576	NUP160, LOC105376598, 2842 more genes
nsv3900144	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 198,510-134,934,063 , GRCh38.p12 chr11: 198,510-135,064,169	NUP160, RTN3, 2833 more genes
nsv3908873	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr11: 230,616-134,938,470 , GRCh38.p12 chr11: 230,616-135,068,576	NUP160, IGHMBP2, 2829 more genes
nsv6315537	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 32,799,481-134,938,470 , GRCh38.p12 chr11: 32,777,935-135,068,576	NUP160, PYGM, 2125 more genes
nsv6315474	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 43,607,886-61,466,671 , GRCh38.p12 chr11: 43,586,336-61,699,199	NUP160, TRR-TCT3-2, 494 more genes
nsv5380725	copy number variation	2	nstd102	human	Pathogenic, Uncertain significance	GRCh37 chr11: 45,827,353-47,804,770 , GRCh38.p12 chr11: 45,805,802-47,783,218	NUP160, MIR4688, 58 more genes
nsv3914563	copy number variation	1	nstd102	human	Likely pathogenic	NCBI36 chr11: 42,705,681-49,113,863 , GRCh37 chr11: 42,749,105-49,157,287 , GRCh38 chr11: 42,727,555-49,135,735	NUP160, ACP2, 143 more genes
nsv3898001	copy number variation	1	nstd102	human	Likely benign	GRCh37 chr11: 47,720,039-48,891,877 , GRCh38.p12 chr11: 47,698,487-48,870,325	NUP160, OR4A46P, 27 more genes
nsv3909806	copy number variation	1	nstd102	human	Benign	GRCh37 chr11: 47,825,128-48,601,837 , GRCh38.p12 chr11: 47,803,576-48,580,285	NUP160, OR4A47, 22 more genes
nsv3900305	copy number variation	1	nstd102	human	Benign	GRCh37 chr11: 47,760,768-48,518,893 , GRCh38.p12 chr11: 47,739,216-48,497,341	NUP160, OR4X2, 20 more genes
nsv3906883	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr11: 47,711,244-48,976,284 , GRCh38.p12 chr11: 47,689,692-48,954,732	NUP160, OR4C2P, 30 more genes
nsv3891602	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr11: 47,748,831-48,985,791 , GRCh38.p12 chr11: 47,727,279-48,964,239	NUP160, OR4A41P, 29 more genes
nsv3912772	copy number variation	1	nstd102	human	Uncertain significance	GRCh38 chr11: 47,743,903-48,643,003 , GRCh37 chr11: 47,765,455-48,664,555 , NCBI36 chr11: 47,722,031-48,621,131	NUP160, OR4A48P, 26 more genes
nsv3902059	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr11: 47,773,563-48,403,235 , GRCh38.p12 chr11: 47,752,011-48,381,683	NUP160, LOC100287189, 13 more genes

Supplemental Content

Filters: Manage Filters

Find related data

Search details

Recent activity

Clear Turn Off Turn On

nup160[All Fields] AND 1[has_clinical] (20)
dbVar
HHS in the 21st Century
HHS in the 21st Century

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)