OSC3770 AND nstd224 - dbVar - NCBI

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

Search results

Items: 13

loading data ...

Number of Variants: 13

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv6630626	copy number variation	240	nstd224	human		GRCh37 chr5: 97,061,761-97,096,042 , GRCh38.p12 chr5: 97,726,057-97,760,338	LOC391813
nsv6622704	copy number variation	29	nstd224	human		GRCh37 chr14: 24,453,366-24,464,590 , GRCh38.p12 chr14: 23,984,157-23,995,381 , GRCh38.p12 chr14\|NW_018654722.1: 290,491-301,715	DHRS4L2
nsv6625369	copy number variation	22	nstd224	human		GRCh37 chr1: 12,907,689-12,921,278 , GRCh38.p12 chr1: 12,847,836-12,861,423 , GRCh38.p12 chr1\|NW_012132914.1: 29,349-42,936	PRAMEF2, HNRNPCL1
nsv6626508	copy number variation	1	nstd224	human		GRCh37 chr20: 14,863,658-14,928,020 , GRCh38.p12 chr20: 14,883,012-14,947,374	MACROD2-AS1, MACROD2
nsv6620379	copy number variation	16	nstd224	human		GRCh37 chr10: 46,965,017-47,115,057 , GRCh38.p12 chr10: 46,434,696-46,584,600	GPRIN2, NPY4R, 3 more genes
nsv6628340	copy number variation	1	nstd224	human		GRCh37 chr2: 75,425,755-75,608,486 , GRCh38.p12 chr2: 75,198,629-75,381,360	TACR1, LOC105374810, 2 more genes
nsv6630373	copy number variation	42	nstd224	human		GRCh37 chr5: 744,005-825,329 , GRCh38.p12 chr5: 743,890-825,214	ZDHHC11B, ZDHHC11, 1 more genes
nsv6633920	copy number variation	98	nstd224	human		GRCh37 chr9: 5,306,824-5,335,570 , GRCh38.p12 chr9: 5,306,824-5,335,570	RLN1, RLN2, 1 more genes
nsv6624267	copy number variation	1	nstd224	human		GRCh37 chr17: 3,301,421-3,533,547 , GRCh38.p12 chr17: 3,398,127-3,630,253	ASPA, TRPV1, 7 more genes
nsv6631445	copy number variation	586	nstd224	human		GRCh37 chr6: 67,017,543-67,044,431 , GRCh38.p12 chr6: 66,307,650-66,334,538	0
nsv6630107	copy number variation	584	nstd224	human		GRCh37 chr5: 140,223,185-140,238,124 , GRCh38.p12 chr5: 140,843,600-140,858,539	PCDHA4, PCDHA1, 9 more genes
nsv6626303	copy number variation	1	nstd224	human		GRCh37 chr20: 12,790,887-13,251,388 , GRCh38.p12 chr20: 12,810,239-13,270,741	SPTLC3, TASP1, 7 more genes
nsv6623615	copy number variation	320	nstd224	human		GRCh37 chr16: 34,516,075-34,686,820 , GRCh38.p12 chr16: 35,281,704-35,452,449	AGGF1P4, FRG2IP, 14 more genes

Supplemental Content

Filters: Manage Filters

Find related data

Search details

Recent activity

Clear Turn Off Turn On

OSC3770 AND nstd224 (14)
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)