OSC7392 AND nstd224 - dbVar - NCBI

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

Search results

Items: 10

loading data ...

Number of Variants: 10

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv6630814	copy number variation	62	nstd224	human		GRCh37 chr5: 97,051,856-97,096,042 , GRCh38.p12 chr5: 97,716,152-97,760,338	LOC391813
nsv6630339	copy number variation	71	nstd224	human		GRCh37 chr5: 32,120,277-32,160,019 , GRCh38.p12 chr5: 32,120,171-32,159,913	GOLPH3
nsv6623651	copy number variation	160	nstd224	human		GRCh37 chr16: 32,509,483-32,650,542 , GRCh38.p12 chr16: 32,498,162-32,639,221	FAM153DP, LOC107984013
nsv6624685	copy number variation	256	nstd224	human		GRCh37 chr19: 20,605,360-20,700,135 , GRCh38.p12 chr19: 20,422,554-20,517,329	BNIP3P23, LOC105372317, 2 more genes
nsv6627380	copy number variation	480	nstd224	human		GRCh37 chr22: 24,374,253-24,390,432 , GRCh38.p12 chr22\|NT_187633.1: 268,428-284,607	GSTTP2, GSTT1-AS1, 2 more genes
nsv6625708	copy number variation	11	nstd224	human		GRCh37 chr1: 195,832,109-195,868,725 , GRCh38.p12 chr1: 195,862,979-195,899,595	0
nsv6633430	copy number variation	152	nstd224	human		GRCh37 chr9: 24,505,147-24,518,795 , GRCh38.p12 chr9: 24,505,149-24,518,797	0
nsv6624243	copy number variation	9	nstd224	human		GRCh37 chr17: 44,187,257-44,353,222 , GRCh38.p12 chr17: 46,109,891-46,275,856 , GRCh38.p12 chr17\|NT_187663.1: 811,990-954,783	KANSL1, KANSL1-AS1, 5 more genes
nsv6623664	copy number variation	56	nstd224	human		GRCh37 chr16: 34,489,371-34,732,946 , GRCh38.p12 chr16: 35,255,000-35,498,575	LINC01566, AGGF1P9, 21 more genes
nsv6627895	copy number variation	12	nstd224	human		GRCh37 chr2: 57,402,202-57,455,549 , GRCh38.p12 chr2: 57,175,067-57,228,414	0

Supplemental Content

Filters: Manage Filters

Find related data

Search details

Recent activity

Clear Turn Off Turn On

OSC7392 AND nstd224 (11)
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)