CONTROL_14 AND nstd53 - 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
nsv869990	copy number variation	71	nstd53	human		GRCh38.p12 chr6: 32,512,052-32,529,545 , NCBI36 chr6: 32,587,807-32,605,300 , GRCh37.p13 chr6: 32,479,829-32,497,322 , GRCh37.p13 chr6\|NT_167245.1: 3,821,149-3,834,945 , GRCh37.p13 chr6\|NT_167246.1: 3,995,584-4,009,378	HLA-DRB5
nsv869730	copy number variation	122	nstd53	human		GRCh38.p12 chr8: 39,377,532-39,528,580 , NCBI36 chr8: 39,354,208-39,505,256 , GRCh37.p13 chr8: 39,235,051-39,386,099	ADAM3A, ADAM5
nsv870126	copy number variation	3	nstd53	human		GRCh38.p12 chr10: 44,723,391-44,871,473 , NCBI36 chr10: 44,538,845-44,686,927 , GRCh37.p13 chr10: 45,218,839-45,366,921	TMEM72-AS1, EIF2AP4
nsv869967	copy number variation	8	nstd53	human		NCBI36 chrX: 103,148,283-103,183,992 , GRCh37.p13 chrX: 103,261,627-103,297,336 , GRCh38.p12 chrX: 104,007,055-104,042,769 , GRCh37.p13 chrX\|NW_004070885.1: 143,471-179,185	H2BW1, H2BW2
nsv869807	copy number variation	87	nstd53	human		NCBI36 chr11: 55,118,273-55,200,744 , GRCh37.p13 chr11: 55,361,697-55,444,168 , GRCh38.p12 chr11: 55,594,221-55,676,692	OR4V1P, OR4P4, 3 more genes
nsv870166	copy number variation	20	nstd53	human		NCBI36 chr14: 73,061,897-73,101,327 , GRCh38.p12 chr14: 73,525,440-73,564,870 , GRCh37.p13 chr14: 73,992,144-74,031,574	NT5CP2, HEATR4, 1 more genes
nsv870111	copy number variation	3	nstd53	human		NCBI36 chr20: 43,783,621-43,813,650 , GRCh37.p13 chr20: 44,350,207-44,380,243 , GRCh38.p12 chr20: 45,721,568-45,751,604	WFDC3, SPINT5P, 2 more genes
nsv869870	copy number variation	1	nstd53	human		NCBI36 chr11: 133,854,151-134,225,495 , GRCh37.p13 chr11: 134,348,941-134,720,285 , GRCh38.p12 chr11: 134,479,047-134,850,391	B3GAT1-DT, LINC02714, 2 more genes
nsv869672	copy number variation	3	nstd53	human		NCBI36 chr14: 105,026,176-105,071,694 , GRCh38.p12 chr14: 105,488,794-105,533,002 , GRCh37.p13 chr14: 105,955,131-106,000,649 , GRCh37.p13 chr14\|NW_004166863.1: 151,961-197,479	CRIP1, TMEM121, 2 more genes
nsv870009	copy number variation	36	nstd53	human		GRCh37.p13 chr3: 195,354,183-195,457,709 , GRCh38.p12 chr3: 195,627,312-195,730,838 , NCBI36 chr3: 196,835,472-196,943,380 , GRCh38.p12 chr3\|NT_187649.1: 63,861-139,787 , GRCh38.p12 chr3\|NT_187688.1: 63,861-140,349 , GRCh38.p12 chr3\|NT_187690.1: 63,868-141,061 , GRCh38.p12 chr3\|NT_187691.1: 64,038-142,498 , GRCh38.p12 chr3\|NT_187678.1: 65,206-143,431 , GRCh38.p12 chr3\|NT_187689.1: 23,110-101,335 , GRCh38.p12 chr3\|NT_187532.1: 23,110-101,335	MUC20, MIR570HG, 7 more genes
nsv869711	copy number variation	90	nstd53	human		NCBI36 chr4: 69,099,876-69,643,272 , GRCh37.p13 chr: NaN-NaN , GRCh38.p12 chr: NaN-NaN	0
nsv870016	copy number variation	3	nstd53	human		GRCh37.p13 chr3: 162,526,686-162,630,179 , GRCh38.p12 chr3: 162,808,898-162,912,391 , NCBI36 chr3: 164,009,380-164,112,873	0
nsv869637	copy number variation	57	nstd53	human		NCBI36 chr14: 105,606,483-105,623,070 , GRCh37.p13 chr14: 106,535,438-106,552,025 , GRCh38.p12 chr: NaN-NaN	0
nsv870162	copy number variation	5	nstd53	human		NCBI36 chr5: 738,300-873,365 , GRCh37.p13 chr5: 685,300-820,365 , GRCh38.p12 chr5: 685,185-820,250	TPPP, ZDHHC11, 4 more genes

Supplemental Content

Filters: Manage Filters

Find related data

Search details

Recent activity

Clear Turn Off Turn On

CONTROL_14 AND nstd53 (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)