CONTROL_90 AND nstd53 - dbVar - NCBI

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

Search results

Items: 17

loading data ...

Number of Variants: 17

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv870077	copy number variation	2	nstd53	human		GRCh38.p12 chr6: 124,014,151-124,035,667 , NCBI36 chr6: 124,376,995-124,398,511 , GRCh37.p13 chr6: 124,335,296-124,356,812	NKAIN2
nsv870214	copy number variation	3	nstd53	human		NCBI36 chr7: 142,526,312-142,605,735 , GRCh37.p13 chr7: 142,816,190-142,895,613 , GRCh38.p12 chr7: 143,119,097-143,198,520	PIP, TAS2R39
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
nsv870358	copy number variation	4	nstd53	human		NCBI36 chr12: 11,395,921-11,435,643 , GRCh38.p12 chr12: 11,351,720-11,391,442 , GRCh37.p13 chr12: 11,504,654-11,544,376 , GRCh38.p12 chr12\|NT_187658.1: 546,683-572,349	PRB1, PRB2
nsv870293	copy number variation	20	nstd53	human		NCBI36 chr1: 246,794,611-246,864,725 , GRCh38.p12 chr1: 248,564,687-248,634,801 , GRCh37.p13 chr1: 248,727,988-248,798,102	OR2T34, OR2T10, 1 more genes
nsv869972	copy number variation	12	nstd53	human		NCBI36 chr12: 10,457,222-10,493,984 , GRCh38.p12 chr12: 10,413,356-10,450,118 , GRCh37.p13 chr12: 10,565,955-10,602,717	KLRC1, KLRC2, 1 more genes
nsv869920	copy number variation	3	nstd53	human		GRCh37.p13 chr3: 100,336,028-100,437,968 , GRCh38.p12 chr3: 100,617,184-100,719,124 , NCBI36 chr3: 101,818,718-101,920,658	TFG, ADGRG7, 1 more genes
nsv869948	copy number variation	4	nstd53	human		GRCh38.p12 chr2: 232,376,334-232,415,460 , NCBI36 chr2: 232,949,288-232,988,414 , GRCh37.p13 chr2: 233,241,044-233,280,170	ALPP, ALPG, 3 more genes
nsv870265	copy number variation	100	nstd53	human		NCBI36 chr22: 22,696,215-22,725,305 , GRCh37.p13 chr22: 24,366,215-24,395,305 , GRCh38.p12 chr22\|NT_187633.1: 260,390-289,480	GSTT1, LOC391322, 3 more genes
nsv869695	copy number variation	4	nstd53	human		NCBI36 chr7: 142,156,215-142,176,074 , GRCh38.p12 chr7\|NT_187562.1: 771,386-791,246 , GRCh37.p13 chr7\|NW_003571040.1: 951,457-971,317	TRB, PRSS3P2, 1 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
nsv869669	copy number variation	15	nstd53	human		GRCh38.p12 chr6: 32,487,556-32,669,281 , NCBI36 chr6: 32,563,311-32,745,036 , GRCh37.p13 chr6: 32,455,333-32,637,058 , GRCh37.p13 chr6\|NT_167245.1: 3,821,149-3,914,321 , GRCh38.p12 chr6\|NT_167246.2: 3,824,251-4,063,916 , GRCh37.p13 chr6\|NT_167246.1: 3,827,971-4,069,536 , GRCh38.p12 chr6\|NT_167247.2: 3,858,983-3,965,783 , GRCh37.p13 chr6\|NT_167247.1: 3,864,568-3,971,368 , GRCh37.p13 chr6\|NT_167249.1: 3,832,679-4,064,436 , GRCh38.p12 chr6\|NT_167249.2: 3,833,381-4,065,138	HLA-DQA1, HLA-DQB1, 17 more genes
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
nsv869703	copy number variation	13	nstd53	human		NCBI36 chr16: 34,329,577-34,619,028 , GRCh38.p12 chr16: 35,237,705-35,527,156 , GRCh37.p13 chr16: 34,472,076-34,761,527	FRG2DP, LINC01566, 25 more genes
nsv869782	copy number variation	92	nstd53	human		NCBI36 chr14: 19,273,348-19,478,367 , GRCh38.p12 chr14: 19,735,349-19,940,368 , GRCh37.p13 chr14: 20,203,508-20,408,527	OR4K6P, OR4K5, 10 more genes
nsv869762	copy number variation	17	nstd53	human		GRCh37.p13 chr3: 162,540,867-162,630,179 , GRCh38.p12 chr3: 162,823,079-162,912,391 , NCBI36 chr3: 164,023,561-164,112,873	0

Supplemental Content

Filters: Manage Filters

Find related data

Search details

Recent activity

Clear Turn Off Turn On

CONTROL_90 AND nstd53 (18)
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)