IS30653 AND nstd71 - dbVar - NCBI

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

Search results

Items: 12

loading data ...

Number of Variants: 12

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv876387	copy number variation	10	nstd71	human		NCBI36 chr3: 2,183,832-2,256,628 , GRCh37.p13 chr3: 2,208,832-2,281,628 , GRCh38.p12 chr3: 2,167,148-2,239,944	CNTN4
nsv884818	copy number variation	499	nstd71	human		NCBI36 chr6: 32,560,168-32,591,507 , GRCh37.p13 chr6: 32,452,190-32,483,529 , GRCh38.p12 chr6: 32,484,413-32,515,752	HLA-DRB5
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
nsv911944	copy number variation	4	nstd71	human		NCBI36 chr19: 48,066,441-48,160,500 , GRCh37.p13 chr19: 43,374,601-43,468,660 , GRCh38.p12 chr19: 42,870,449-42,964,508	CEACAMP7, PSG1, 2 more genes
nsv907834	copy number variation	20	nstd71	human		NCBI36 chr17: 18,954,494-18,999,864 , GRCh37.p13 chr17: 19,013,769-19,059,139 , GRCh38.p12 chr17: 19,110,456-19,155,826	GRAPL-AS1, SNORD3D, 1 more genes
nsv871196	copy number variation	88	nstd71	human		NCBI36 chr1: 12,777,429-12,810,136 , GRCh37.p13 chr1: 12,854,842-12,887,549 , GRCh38.p12 chr1: 12,794,693-12,827,690	PRAMEF11, PRAMEF1, 1 more genes
nsv876259	copy number variation	2	nstd71	human		NCBI36 chr2: 242,429,063-242,602,539 , GRCh37.p13 chr2: 242,780,390-242,953,866 , GRCh38.p12 chr2: 241,838,238-242,011,715 , GRCh38.p12 chr2\|NT_187527.1: 50,336-174,166	LOC105373978, LOC285097, 6 more genes
nsv914206	copy number variation	75	nstd71	human		NCBI36 chr22: 17,242,612-17,396,663 , GRCh37.p13 chr22: 18,862,612-19,016,663 , GRCh38.p12 chr22: 18,875,099-19,029,150	FAM230F, DGCR6, 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
nsv874633	copy number variation	47	nstd71	human		NCBI36 chr2: 89,721,421-89,885,025 , GRCh37.p13 chr2: 90,084,116-90,247,720 , GRCh38.p12 chr2: 90,045,284-90,208,854	IGKV1D-43, IGKV2D-18, 12 more genes
nsv876893	copy number variation	298	nstd71	human		NCBI36 chr3: 65,159,939-65,190,844 , GRCh37.p13 chr3: 65,184,899-65,215,804 , GRCh38.p12 chr3: 65,199,224-65,230,129	0
nsv915172	copy number variation	84	nstd71	human		NCBI36 chr22: 21,047,055-21,075,525 , GRCh37.p13 chr22: 22,717,055-22,745,525 , GRCh38.p12 chr22\|NT_187629.1: 1-17,710 , GRCh38.p12 chr22: 22,362,695-22,391,157	IGLV7-46, IGLV1-44, 4 more genes

Supplemental Content

Filters: Manage Filters

Find related data

Search details

Recent activity

Clear Turn Off Turn On

IS30653 AND nstd71 (13)
dbVar
IS38304 AND nstd71 (8)
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)