NA18502 AND nstd20 - dbVar - NCBI

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

Search results

Items: 15

loading data ...

Number of Variants: 15

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv438136	copy number variation	6	nstd20	human		NCBI34 chrX: 65,105,136-65,531,010 , GRCh37.p13 chrX: 66,238,345-66,664,219 , GRCh38.p12 chrX: 67,018,503-67,444,377	LOC100129144
nsv438048	copy number variation	78	nstd20	human		NCBI34 chr1: 149,771,758-149,800,260 , GRCh37.p13 chr1: 152,555,176-152,583,678 , GRCh38.p12 chr1: 152,582,700-152,611,202	LCE3C
nsv438263	copy number variation	3	nstd20	human		NCBI34 chr14: 74,338,282-74,350,474 , GRCh37.p13 chr14: 76,348,241-76,360,433 , GRCh38.p12 chr14: 75,881,898-75,894,090	TTLL5
nsv438381	copy number variation	2	nstd20	human		NCBI34 chr2: 209,437,916-209,442,285 , GRCh37.p13 chr2: 209,235,373-209,239,742 , GRCh38.p12 chr2: 208,370,648-208,375,017	PTH2R
nsv437970	copy number variation	6	nstd20	human		NCBI34 chr1: 10,084,725-10,087,962 , GRCh37.p13 chr1: 10,375,179-10,378,416 , GRCh38.p12 chr1: 10,315,121-10,318,358	KIF1B
nsv438130	copy number variation	4	nstd20	human		NCBI34 chrX: 46,532,540-46,534,975 , GRCh37.p13 chrX: 47,486,558-47,488,993 , GRCh38.p12 chrX: 47,627,159-47,629,594	CFP
nsv438126	copy number variation	18	nstd20	human		NCBI34 chr1: 194,080,727-194,081,468 , GRCh37.p13 chr1: 196,792,468-196,793,209 , GRCh38.p12 chr1: 196,823,338-196,824,079	CFHR1
nsv438190	copy number variation	18	nstd20	human		NCBI34 chr12: 11,375,250-11,435,555 , GRCh38.p12 chr12: 11,331,049-11,391,354 , GRCh37.p13 chr12: 11,483,983-11,544,288 , GRCh38.p12 chr12\|NT_187658.1: 526,012-572,349	PRB1, PRB2
nsv438338	copy number variation	81	nstd20	human		NCBI34 chr22: 21,026,944-21,558,650 , GRCh37.p13 chr22: 22,702,390-23,234,096 , GRCh38.p12 chr22: 22,348,040-22,891,916	BCRP4, IGL, 72 more genes
nsv437921	copy number variation	122	nstd20	human		GRCh37.p13 chr: NaN-NaN , GRCh38.p12 chr: NaN-NaN , NCBI34 chr4: 69,377,786-69,808,237	0
nsv437976	copy number variation	55	nstd20	human		NCBI34 chr6: 103,768,785-103,807,031 , GRCh37.p13 chr6: 103,723,215-103,761,461 , GRCh38.p12 chr6: 103,275,340-103,313,586	0
nsv437983	copy number variation	2	nstd20	human		NCBI34 chr7: 12,848,771-12,856,660 , GRCh37.p13 chr7: 13,104,434-13,112,323 , GRCh38.p12 chr7: 13,064,809-13,072,698	0
nsv437919	copy number variation	22	nstd20	human		NCBI34 chr4: 63,672,955-63,678,558 , GRCh37.p13 chr4: 63,669,575-63,675,178 , GRCh38.p12 chr4: 62,803,857-62,809,460	0
nsv437964	copy number variation	6	nstd20	human		NCBI34 chr6: 31,382,098-31,387,190 , GRCh37.p13 chr6\|NT_113891.2: 2,790,607-2,795,699 , GRCh37.p13 chr6\|NT_167247.1: 2,657,879-2,662,962 , GRCh37.p13 chr6\|NT_167248.1: 2,570,878-2,575,945 , GRCh37.p13 chr6\|NT_167249.1: 2,611,106-2,616,172 , GRCh37.p13 chr6\|NT_167246.1: 2,624,194-2,629,281 , GRCh37.p13 chr6: 31,277,368-31,282,462 , GRCh38.p12 chr6: 31,309,591-31,314,685 , GRCh38.p12 chr6\|NT_167247.2: 2,652,294-2,657,377 , GRCh38.p12 chr6\|NT_167248.2: 2,565,282-2,570,349 , GRCh38.p12 chr6\|NT_167249.2: 2,611,808-2,616,874 , GRCh38.p12 chr6\|NT_113891.3: 2,790,501-2,795,593 , GRCh38.p12 chr6\|NT_167246.2: 2,618,574-2,623,661	0
nsv437967	copy number variation	12	nstd20	human		NCBI34 chr6: 33,985,151-33,989,083 , GRCh37.p13 chr6: 33,938,296-33,942,228 , GRCh38.p12 chr6: 33,970,519-33,974,451	0

Supplemental Content

Filters: Manage Filters

Find related data

Search details

Recent activity

Clear Turn Off Turn On

NA18502 AND nstd20 (16)
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)