NA18540 AND nstd20 - dbVar - NCBI

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

Search results

Items: 14

loading data ...

Number of Variants: 14

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv438141	copy number variation	2	nstd20	human		NCBI34 chrX: 83,958,997-83,971,986 , GRCh37.p13 chrX: 85,187,140-85,200,129 , GRCh38.p12 chrX: 85,932,135-85,945,124	CHM
nsv438006	copy number variation	36	nstd20	human		NCBI34 chr7: 133,202,026-133,212,391 , GRCh37.p13 chr7: 133,785,899-133,796,264 , GRCh38.p12 chr7: 134,101,146-134,111,511
nsv437907	copy number variation	146	nstd20	human		NCBI34 chr3: 194,196,286-194,205,086 , GRCh37.p13 chr3: 192,875,373-192,884,173 , GRCh38.p12 chr3: 193,157,584-193,166,384	VEZF1P1
nsv438117	copy number variation	2	nstd20	human		NCBI34 chr9: 136,191,747-136,197,190 , GRCh37.p13 chr9: 140,973,133-140,978,576 , GRCh38.p12 chr9: 138,078,681-138,084,124	CACNA1B
nsv438155	copy number variation	2	nstd20	human		NCBI34 chrX: 121,803,546-121,804,252 , GRCh37.p13 chrX: 123,105,791-123,106,497 , GRCh38.p12 chrX: 123,971,941-123,972,647	STAG2
nsv438153	copy number variation	2	nstd20	human		NCBI34 chrX: 114,373,214-114,373,881 , GRCh37.p13 chrX\|NW_004070892.1: 618,997-619,664 , GRCh37.p13 chrX: 115,589,112-115,589,779 , GRCh38.p12 chrX: 116,457,946-116,458,613	SLC6A14
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
nsv437894	copy number variation	301	nstd20	human		NCBI34 chr3: 163,826,348-163,943,569 , GRCh37.p13 chr3: 162,505,435-162,622,656 , GRCh38.p12 chr3: 162,787,647-162,904,868	0
nsv437892	copy number variation	5	nstd20	human		NCBI34 chr3: 163,538,907-163,550,497 , GRCh37.p13 chr3: 162,217,994-162,229,584 , GRCh38.p12 chr3: 162,500,206-162,511,796	0
nsv438371	copy number variation	55	nstd20	human		NCBI34 chr2: 147,075,728-147,086,685 , GRCh37.p13 chr2: 146,864,959-146,875,916 , GRCh38.p12 chr2: 146,107,391-146,118,348	0
nsv438142	copy number variation	2	nstd20	human		NCBI34 chrX: 84,097,369-84,104,170 , GRCh37.p13 chrX: 85,325,512-85,332,313 , GRCh38.p12 chrX: 86,070,508-86,077,309	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
nsv438005	copy number variation	72	nstd20	human		NCBI34 chr7: 125,601,054-125,603,762 , GRCh37.p13 chr7: 126,046,565-126,049,273 , GRCh38.p12 chr7: 126,406,511-126,409,219	0
nsv438368	copy number variation	10	nstd20	human		NCBI34 chr2: 123,575,969-123,577,446 , GRCh37.p13 chr2: 123,480,824-123,482,301 , GRCh38.p12 chr2: 122,723,248-122,724,725	0

Supplemental Content

Filters: Manage Filters

Find related data

Search details

Recent activity

Clear Turn Off Turn On

NA18540 AND nstd20 (15)
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)