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 105

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7094848copy number variation1nstd102humanUncertain significance GRCh37 chr16: 53,635,988-54,967,785 , GRCh38.p12 chr16: 53,602,076-54,933,873 LOC105371271, LOC105371272, 13 more genes
    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
    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
    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
    nsv6291644copy number variation1nstd102humanUncertain significance GRCh37 chr16: 53,771,653-54,384,400 , GRCh38.p12 chr16: 53,737,741-54,350,488 LOC105371271, FTO-IT1, 3 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
    nsv5656375insertion1nstd207human GRCh38 chr16: 54,282,211-54,282,211 , GRCh37.p13 chr16: 54,316,123-54,316,123 IRX3
    nsv4749427copy number variation1nstd199human GRCh37 chr16: 29,238,132-88,226,311 , GRCh38.p12 chr16: 29,226,811-88,192,705 , ITGAM, 1076 more genes
    nsv4670435copy number variation1nstd186human GRCh37 chr16: 54,316,101-54,325,900 , GRCh38.p12 chr16: 54,282,189-54,291,988 IRX3
    nsv4628037copy number variation1nstd183human GRCh37 chr16: 54,318,165-54,318,764 , GRCh38.p12 chr16: 54,284,253-54,284,852 IRX3
    nsv4627552copy number variation1nstd183human GRCh37 chr16: 54,316,101-54,325,900 , GRCh38.p12 chr16: 54,282,189-54,291,988 IRX3
    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
    nsv4426231copy number variation1nstd174human GRCh37 chr16: 54,315,945-54,326,092 , GRCh38.p12 chr16: 54,282,033-54,292,180 IRX3
    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
    nsv3921269copy number variation1nstd102humanPathogenic NCBI36 chr16: 31,893,599-88,822,254 , GRCh37.p13 chr16: 31,986,098-90,294,753 , GRCh38.p12 chr16: 31,974,777-90,228,345 LOC105371237, IGHV3OR16-11, 985 more genes
    nsv3918594copy number variation1nstd102humanPathogenic GRCh38 chr16: 50,784,329-55,566,715 , NCBI36 chr16: 49,375,741-54,158,128 , GRCh37 chr16: 50,818,240-55,600,627 TOX3, CASC22, 74 more genes
    nsv3918521copy number variation1nstd102humanPathogenic NCBI36 chr16: 48,276,933-66,993,116 , GRCh37 chr16: 49,719,432-68,435,615 , GRCh38 chr16: 49,685,521-68,401,712 CYLD-AS2, MT1F, 342 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