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 135

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7095031copy number variation2nstd102humanPathogenic GRCh37 chr16: 56,226,148-58,768,132 , GRCh38.p12 chr16: 56,192,236-58,734,228 MT1B, LOC105371293, 92 more genes
    nsv7094589copy number variation1nstd102humanPathogenic GRCh37 chr16: 57,016,057-58,768,132 , GRCh38.p12 chr16: 56,982,145-58,734,228 SLC38A7, SETD6, 58 more genes
    nsv6986991copy number variation1nstd229human GRCh38 chr16: 57,059,649-57,664,041 , GRCh37.p13 chr16: 57,093,561-57,697,953 CPNE2, TRL-CAG2-1, 21 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
    nsv6590125inversion1nstd223human GRCh38 chr16: 57,174,286-57,175,261 , GRCh37.p13 chr16: 57,208,198-57,209,173 PSME3IP1
    nsv6590013inversion1nstd223human GRCh38 chr16: 57,183,041-57,183,576 , GRCh37.p13 chr16: 57,216,953-57,217,488 PSME3IP1
    nsv6579946inversion1nstd223human GRCh38 chr16: 57,161,703-57,163,114 , GRCh37.p13 chr16: 57,195,615-57,197,026 PSME3IP1
    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
    nsv6250317mobile element insertion1nstd215human GRCh38 chr16: 57,157,839-57,157,839 , GRCh37.p13 chr16: 57,191,751-57,191,751 PSME3IP1
    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
    nsv5706453mobile element insertion2nstd211human GRCh38 chr16: 57,169,220-57,169,220 , GRCh37.p13 chr16: 57,203,132-57,203,132 PSME3IP1
    nsv5704563mobile element insertion1nstd211human GRCh38 chr16: 57,157,839-57,157,839 , GRCh37.p13 chr16: 57,191,751-57,191,751 PSME3IP1
    nsv5696324mobile element insertion1nstd211human GRCh38 chr16: 57,182,576-57,182,576 , GRCh37.p13 chr16: 57,216,488-57,216,488 PSME3IP1
    nsv5431824mobile element insertion1nstd206human GRCh38 chr16: 57,157,839-57,157,890 , GRCh37.p13 chr16: 57,191,751-57,191,802 PSME3IP1
    nsv5416328mobile element insertion1nstd206human GRCh38 chr16: 57,169,232-57,169,283 , GRCh37.p13 chr16: 57,203,144-57,203,195 PSME3IP1
    nsv5358218translocation1nstd200human GRCh38 chr16: 57,204,503-57,204,503 , GRCh38 chr16: 57,186,451-57,186,451 , GRCh37.p13 chr16: 57,220,363-57,220,363 , GRCh37.p13 chr16: 57,238,415-57,238,415 PSME3IP1, RSPRY1
    nsv5301175copy number variation1nstd204human GRCh38.p13 chr16: 56,771,413-57,511,371 , GRCh37.p13 chr16: 56,805,325-57,545,283 , PLLP, 24 more genes
    nsv5266636copy number variation1nstd204human GRCh38.p13 chr16: 57,174,792-57,176,916 , GRCh37.p13 chr16: 57,208,704-57,210,828 PSME3IP1
    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