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 202

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7142143copy number variation1nstd232human GRCh37.p13 chr16: 58,744,620-58,744,705 , GRCh38.p12 chr16: 58,710,716-58,710,801 GOT2
    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
    nsv7069876inversion1nstd229human GRCh38 chr16: 58,076,774-64,694,512 , GRCh37.p13 chr16: 58,110,678-64,728,415 RN7SKP76, LOC105371311, 57 more genes
    nsv7069696inversion1nstd229human GRCh38 chr16: 58,205,688-64,165,972 , GRCh37.p13 chr16: 58,239,592-64,199,876 GOT2, RNU6-103P, 49 more genes
    nsv7060534inversion1nstd229human GRCh38 chr16: 58,713,481-58,714,210 , GRCh37.p13 chr16: 58,747,385-58,748,114 GOT2
    nsv6997976copy number variation1nstd229human GRCh38 chr16: 58,725,655-58,731,278 , GRCh37.p13 chr16: 58,759,559-58,765,182 GOT2, RNY5P9
    nsv6989404copy number variation1nstd229human GRCh38 chr16: 58,658,584-58,800,393 , GRCh37.p13 chr16: 58,692,488-58,834,297 GOT2, SLC38A7, 5 more genes
    nsv6983412copy number variation1nstd229human GRCh38 chr16: 58,674,529-58,707,335 , GRCh37.p13 chr16: 58,708,433-58,741,239 GOT2, SLC38A7
    nsv6979319copy number variation1nstd229human GRCh38 chr16: 58,671,476-58,711,008 , GRCh37.p13 chr16: 58,705,380-58,744,912 SLC38A7, GOT2
    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
    nsv6637562copy number variation1nstd102humanUncertain significance GRCh37 chr16: 58,728,445-59,190,769 , GRCh38.p12 chr16: 58,694,541-59,156,865 GOT2, RN7SL143P, 7 more genes
    nsv6637265copy number variation1nstd102humanUncertain significance GRCh37 chr16: 58,694,271-58,831,729 , GRCh38.p12 chr16: 58,660,367-58,797,825 GOT2, SLC38A7, 5 more genes
    nsv6623723copy number variation1nstd224human GRCh37 chr16: 58,742,191-59,171,239 , GRCh38.p12 chr16: 58,708,287-59,137,335 GOT2, GEMIN8P2, 7 more genes
    nsv6623682copy number variation1nstd224human GRCh37 chr16: 58,742,190-58,986,204 , GRCh38.p12 chr16: 58,708,286-58,952,300 GOT2, GEMIN8P2, 6 more genes
    nsv6584594inversion1nstd223human GRCh38 chr16: 58,713,348-58,713,440 , GRCh37.p13 chr16: 58,747,252-58,747,344 GOT2
    nsv6576512inversion1nstd223human GRCh38 chr16: 58,734,751-58,735,808 , GRCh37.p13 chr16: 58,768,655-58,769,712 GOT2
    nsv6514677copy number variation1nstd223human GRCh38 chr16: 58,658,584-58,800,395 , GRCh37.p13 chr16: 58,692,488-58,834,299 GOT2, SLC38A7, 5 more genes
    nsv6508740copy number variation1nstd223human GRCh38 chr16: 58,703,741-58,706,477 , GRCh37.p13 chr16: 58,737,645-58,740,381 GOT2
    nsv6498361copy number variation1nstd223human GRCh38 chr16: 58,616,401-58,799,700 , GRCh37.p13 chr16: 58,650,305-58,833,604 GOT2, RNY5P9, 6 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