OSC4082 AND nstd224 - dbVar - NCBI

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

Search results

Items: 9

loading data ...

Number of Variants: 9

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv6623401	copy number variation	1	nstd224	human		GRCh37 chr16: 12,625,171-12,686,917 , GRCh38.p12 chr16: 12,531,314-12,593,060	SNX29, LOC105371085
nsv6624085	copy number variation	3	nstd224	human		GRCh37 chr17: 44,249,096-44,293,020 , GRCh38.p12 chr17: 46,171,730-46,215,654 , GRCh38.p12 chr17\|NT_187663.1: 873,835-917,827	KANSL1-AS1, KANSL1
nsv6624265	copy number variation	1	nstd224	human		GRCh37 chr17: 30,348,167-30,380,381 , GRCh38.p12 chr17: 32,021,148-32,053,362	SH3GL1P1, LRRC37B
nsv6628116	copy number variation	277	nstd224	human		GRCh37 chr2: 38,956,836-38,972,328 , GRCh38.p12 chr2: 38,729,694-38,745,186	SRSF7, GALM
nsv6624990	copy number variation	2	nstd224	human		GRCh37 chr19: 43,372,386-43,528,980 , GRCh38.p12 chr19: 42,868,234-43,024,828	PSG6, CEACAMP7, 3 more genes
nsv6620485	copy number variation	471	nstd224	human		GRCh37 chr10: 47,543,322-47,703,946 , GRCh38.p12 chr10: 46,172,086-46,332,710	AHCYP1, ANTXRL, 2 more genes
nsv6624930	copy number variation	25	nstd224	human		GRCh37 chr19: 43,262,353-43,344,686 , GRCh38.p12 chr19: 42,758,201-42,840,534	CEACAMP6, PSG8-AS1, 2 more genes
nsv6627660	copy number variation	269	nstd224	human		GRCh37 chr2: 242,917,734-243,034,519 , GRCh38.p12 chr2: 241,975,583-242,092,368 , GRCh38.p12 chr2\|NT_187523.1: 14,278-136,438 , GRCh38.p12 chr2\|NT_187647.1: 14,278-136,078	LOC285097, LINC01881, 4 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

OSC4082 AND nstd224 (10)
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)