U.S. flag

An official website of the United States government

Format
Items per page

Send to:

Choose Destination

Links from Gene

Items: 1 to 20 of 238

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7099187copy number variation1nstd231human GRCh38.p12 chr1: 24,354,009-27,158,528 , GRCh37 chr1: 24,680,499-27,485,019 RUNX3, CD52, 88 more genes
    nsv7044760inversion1nstd229human GRCh38 chr1: 22,155,852-26,348,296 , GRCh37.p13 chr1: 22,482,345-26,674,787 MIR4684, PDIK1L, 120 more genes
    nsv6647819copy number variation1nstd229human GRCh38 chr1: 24,438,321-24,466,726 , GRCh37.p13 chr1: 24,764,811-24,793,216 NIPAL3
    nsv6647816copy number variation1nstd229human GRCh38 chr1: 24,407,201-24,760,500 , GRCh37.p13 chr1: 24,733,691-25,086,991 NCMAP, RCAN3AS, 7 more genes
    nsv6647689copy number variation1nstd229human GRCh38 chr1: 24,431,959-24,432,091 , GRCh37.p13 chr1: 24,758,449-24,758,581 NIPAL3
    nsv6647688copy number variation1nstd229human GRCh38 chr1: 24,426,077-24,445,138 , GRCh37.p13 chr1: 24,752,567-24,771,628 NIPAL3
    nsv6647687copy number variation1nstd229human GRCh38 chr1: 24,420,201-24,459,400 , GRCh37.p13 chr1: 24,746,691-24,785,890 NIPAL3
    nsv6647294copy number variation1nstd229human GRCh38 chr1: 24,447,201-24,454,700 , GRCh37.p13 chr1: 24,773,691-24,781,190 NIPAL3
    nsv6647254copy number variation1nstd229human GRCh38 chr1: 21,562,611-27,513,090 , GRCh37.p13 chr1: 21,889,104-27,839,601 RPL18AP5, LINC00339, 184 more genes
    nsv6647227copy number variation1nstd229human GRCh38 chr1: 20,848,934-27,947,465 , GRCh37.p13 chr1: 21,175,427-28,273,976 RPL17P9, ALPL, 218 more genes
    nsv6636637copy number variation1nstd102humanUncertain significance GRCh37 chr1: 24,363,507-24,875,537 , GRCh38.p12 chr1: 24,037,017-24,549,046 LOC105376864, GRHL3, 13 more genes
    nsv6549480inversion1nstd223human GRCh38 chr1: 24,436,769-24,437,247 , GRCh37.p13 chr1: 24,763,259-24,763,737 NIPAL3
    nsv6335352copy number variation1nstd223human GRCh38 chr1: 24,448,776-24,449,815 , GRCh37.p13 chr1: 24,775,266-24,776,305 NIPAL3
    nsv6333177copy number variation1nstd223human GRCh38 chr1: 24,436,861-24,437,196 , GRCh37.p13 chr1: 24,763,351-24,763,686 NIPAL3
    nsv6332341copy number variation1nstd223human GRCh38 chr1: 24,456,603-24,461,672 , GRCh37.p13 chr1: 24,783,093-24,788,162 NIPAL3
    nsv6331727copy number variation1nstd223human GRCh38 chr1: 24,461,245-24,461,732 , GRCh37.p13 chr1: 24,787,735-24,788,222 NIPAL3
    nsv6319791copy number variation1nstd223human GRCh38 chr1: 24,461,828-24,463,083 , GRCh37.p13 chr1: 24,788,318-24,789,573 NIPAL3
    nsv6315431copy number variation1nstd102humanPathogenic GRCh37 chr1: 24,531,639-24,749,706 , GRCh38.p12 chr1: 24,205,149-24,423,216 STPG1, LINC02800, 3 more genes
    nsv6138874copy number variation1nstd206human GRCh38 chr1: 24,461,307-24,461,632 , GRCh37.p13 chr1: 24,787,797-24,788,122 NIPAL3
    nsv6133992copy number variation1nstd213human GRCh37 chr1: 24,730,000-24,800,001 , GRCh38.p12 chr1: 24,403,510-24,473,511 NIPAL3, STPG1
    Format
    Items per page

    Send to:

    Choose Destination

    Supplemental Content

    Filters: Manage Filters

    Find related data

    Recent activity

    Clear Turn Off Turn On

    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)
    Support Center