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 102

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7138664copy number variation1nstd232human GRCh37.p13 chr16: 55,359,413-55,359,480 , GRCh38.p12 chr16: 55,325,501-55,325,568 IRX6
    nsv7094675copy number variation1nstd102humanPathogenic GRCh37 chr16: 53,635,988-55,539,614 , GRCh38.p12 chr16: 53,602,076-55,505,702 LOC105371276, LINC02183, 22 more genes
    nsv7063904inversion1nstd229human GRCh38 chr16: 54,352,554-57,044,545 , GRCh37.p13 chr16: 54,386,466-57,078,457 LOC102725116, OGFOD1, 65 more genes
    nsv6637586copy number variation1nstd102humanPathogenic GRCh37 chr16: 46,503,573-62,203,182 , GRCh38.p12 chr16: 46,469,661-62,169,278 LINC02140, LOC100130602, 279 more genes
    nsv6315493copy number variation1nstd102humanPathogenic GRCh37 chr16: 55,054,348-56,403,200 , GRCh38.p12 chr16: 55,020,436-56,369,288 LOC102725116, LOC105371281, 21 more genes
    nsv6315060copy number variation1nstd102humanPathogenic GRCh38 chr16: 53,818,483-57,631,312 , GRCh37.p13 chr16: 53,852,395-57,665,224 LOC105371283, MT1A, 91 more genes
    nsv6314755copy number variation1nstd102humanPathogenic GRCh37 chr16: 46,503,968-90,155,062 , GRCh38.p12 chr16: 46,470,056-90,088,654 ATMIN, ATP6V0D1, 826 more genes
    nsv6289807copy number variation1nstd102humanPathogenic GRCh38 chr16: 54,801,236-55,533,834 , GRCh37.p13 chr16: 54,835,148-55,567,746 LOC105371278, LOC105371275, 13 more genes
    nsv6289796copy number variation1nstd102humanPathogenic GRCh38 chr16: 54,893,325-55,501,091 , GRCh37.p13 chr16: 54,927,237-55,535,003 MMP2, CRNDE, 10 more genes
    nsv6133200copy number variation1nstd213human GRCh37 chr16: 46,460,000-84,740,001 , GRCh38.p12 chr16: 46,426,088-84,706,395 , AARS1, 674 more genes
    nsv6112700copy number variation1nstd102humanPathogenic GRCh38 chr16: 46,385,317-61,223,349 , GRCh37.p13 chr16: 46,419,229-61,257,253 CPNE2, USB1, 275 more genes
    nsv6094162insertion1nstd212human GRCh38 chr16: 55,325,530-55,325,530 , GRCh37.p13 chr16: 55,359,442-55,359,442 IRX6
    nsv5970270insertion1nstd209human GRCh38 chr16: 55,325,485-55,325,485 , GRCh37.p13 chr16: 55,359,397-55,359,397 IRX6
    nsv5158944mobile element insertion1nstd203human GRCh38 chr16: 55,325,464-55,325,464 , GRCh37.p13 chr16: 55,359,376-55,359,376 IRX6
    nsv4756658insertion1nstd199human GRCh37 chr16: 55,359,370-55,359,370 , GRCh38.p12 chr16: 55,325,458-55,325,458 IRX6
    nsv4749427copy number variation1nstd199human GRCh37 chr16: 29,238,132-88,226,311 , GRCh38.p12 chr16: 29,226,811-88,192,705 , ITGAM, 1076 more genes
    nsv4508260mobile element insertion1nstd166human GRCh37.p13 chr16: 55,361,869-55,361,869 , GRCh38.p12 chr16: 55,327,957-55,327,957 IRX6
    nsv4456077copy number variation1nstd102humanUncertain significance GRCh37 chr16: 53,455,650-64,006,604 , GRCh38.p12 chr16: 53,421,738-63,972,700 MT1DP, RPL23AP91, 167 more genes
    nsv4365843copy number variation1nstd173human GRCh37 chr16: 46,464,489-55,795,214 , GRCh38.p12 chr16: 46,430,577-55,761,302 , LOC100526838, 158 more genes
    nsv4365186copy number variation1nstd173human GRCh37 chr16: 46,503,205-57,376,253 , GRCh38.p12 chr16: 46,469,293-57,342,341 , TOX3, 210 more genes
    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