M2506 AND nstd157 - 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
nsv3317766	copy number variation	1	nstd157	human		GRCh37 chr20: 31,313,065-31,335,246 , GRCh38.p12 chr20: 32,725,258-32,747,440	COMMD7
nsv3317926	copy number variation	1	nstd157	human		GRCh37 chr16: 60,078,252-60,098,544 , GRCh38.p12 chr16: 60,044,348-60,064,640	LINC02141
nsv3318674	copy number variation	4	nstd157	human		GRCh37 chr14: 63,956,512-63,962,909 , GRCh38.p12 chr14: 63,489,794-63,496,191	PPP2R5E
nsv3318953	copy number variation	35	nstd157	human		GRCh37 chr3: 53,032,639-53,038,786 , GRCh38.p12 chr3: 52,998,623-53,004,770	SFMBT1
nsv3317976	copy number variation	2	nstd157	human		GRCh37 chr4: 25,557,047-25,577,824 , GRCh38.p12 chr4: 25,555,425-25,576,202	LOC101929161
nsv3318924	copy number variation	14	nstd157	human		GRCh38.p12 chr15: 97,271,952-97,288,602 , GRCh37 chr15: 97,815,182-97,831,832	LOC105371006, LINC02253
nsv3317440	copy number variation	2	nstd157	human		GRCh38.p12 chr16: 2,923,248-2,935,683 , GRCh37 chr16: 2,973,249-2,985,684	FLYWCH1, RPL23AP86
nsv3318971	copy number variation	1	nstd157	human		GRCh37 chr17: 16,576,609-16,587,108 , GRCh38.p12 chr17: 16,673,295-16,683,794	CCDC144A, RNASEH1P2
nsv3318588	copy number variation	20	nstd157	human		GRCh38.p12 chr2: 38,729,805-38,744,481 , GRCh37 chr2: 38,956,947-38,971,623	SRSF7, GALM
nsv3317674	copy number variation	4	nstd157	human		GRCh37 chr3: 100,340,145-100,441,716 , GRCh38.p12 chr3: 100,621,301-100,722,872	TFG, ADGRG7, 1 more genes
nsv3317336	copy number variation	2	nstd157	human		GRCh37 chr7: 65,414,031-65,464,524 , GRCh38.p12 chr7: 65,949,044-65,999,537	GUSB, VKORC1L1, 1 more genes
nsv3317581	copy number variation	1	nstd157	human		GRCh37 chr8: 111,756,273-112,432,365 , GRCh38.p12 chr8: 110,744,044-111,420,136	NDUFB9P3, EEF1A1P37, 9 more genes
nsv3318502	copy number variation	31	nstd157	human		GRCh37 chr9: 78,004,378-78,011,616 , GRCh38.p12 chr9: 75,389,462-75,396,700	0
nsv3317472	copy number variation	5	nstd157	human		GRCh38.p12 chr21: 10,653,806-10,746,000 , GRCh37 chr21: 10,766,457-10,858,651	0
nsv3317767	copy number variation	8	nstd157	human		GRCh38.p12 chr2: 57,172,695-57,219,277 , GRCh37 chr2: 57,399,830-57,446,412	0

Supplemental Content

Filters: Manage Filters

Find related data

Search details

Recent activity

Clear Turn Off Turn On

M2506 AND nstd157 (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)