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 197

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5919690copy number variation1nstd209human GRCh38 chr8: 110,927,749-110,931,953 , GRCh37.p13 chr8: 111,939,978-111,944,182 MTCO1P47
    nsv5851765copy number variation2nstd209human GRCh38 chr8: 110,927,758-110,932,119 , GRCh37.p13 chr8: 111,939,987-111,944,348 MTCO1P47
    nsv5576798copy number variation1nstd207human GRCh38 chr8: 110,927,749-110,931,953 , GRCh37.p13 chr8: 111,939,978-111,944,182 MTCO1P47
    nsv5484244copy number variation1nstd206human GRCh38 chr8: 110,927,751-110,931,954 , GRCh37.p13 chr8: 111,939,980-111,944,183 MTCO1P47
    nsv5319337copy number variation1nstd204human GRCh38.p13 chr8: 110,927,746-110,931,958 , GRCh37.p13 chr8: 111,939,975-111,944,187 MTCO1P47
    nsv5252779copy number variation1nstd204human GRCh38.p13 chr8: 110,927,701-110,931,900 , GRCh37.p13 chr8: 111,939,930-111,944,129 MTCO1P47
    nsv5242316copy number variation1nstd204human GRCh38.p13 chr8: 110,927,733-110,931,644 , GRCh37.p13 chr8: 111,939,962-111,943,873 MTCO1P47
    nsv5036483inversion1nstd200human GRCh38 chr8: 71,454,844-121,935,245 , GRCh37.p13 chr8: 72,367,079-122,947,484 , LINC01617, 636 more genes
    nsv5035989inversion1nstd200human GRCh38 chr8: 74,949,087-131,777,713 , GRCh37.p13 chr8: 75,861,322-132,789,960 , MIR7705, 715 more genes
    nsv4965719copy number variation1nstd200human GRCh38 chr8: 110,912,963-111,174,643 , GRCh37.p13 chr8: 111,925,192-112,186,872 LINC01609, MTCO1P47, 3 more genes
    nsv4965716copy number variation1nstd200human GRCh38 chr8: 110,370,859-111,338,035 , GRCh37.p13 chr8: 111,383,088-112,350,264 EEF1A1P37, LOC105375705, 8 more genes
    nsv4961905copy number variation1nstd200human GRCh38 chr8: 110,927,751-110,931,954 , GRCh37.p13 chr8: 111,939,980-111,944,183 MTCO1P47
    nsv4961902copy number variation1nstd200human GRCh38 chr8: 110,885,638-111,179,985 , GRCh37.p13 chr8: 111,897,867-112,192,214 LINC01608, LINC01609, 4 more genes
    nsv4829242copy number variation1nstd200human GRCh37 chr8: 111,383,088-112,350,264 , GRCh38.p12 chr8: 110,370,859-111,338,035 LOC105375705, EEF1A1P37, 8 more genes
    nsv4827659copy number variation1nstd200human GRCh37 chr8: 111,939,980-111,944,183 , GRCh38.p12 chr8: 110,927,751-110,931,954 MTCO1P47
    nsv4729071copy number variation1nstd102humanPathogenic GRCh37 chr8: 108,421,573-123,429,638 , GRCh38.p12 chr8: 107,409,345-122,417,399 RN7SL396P, LOC107986970, 124 more genes
    nsv4684251copy number variation1nstd102humanUncertain significance GRCh37 chr8: 111,417,315-112,383,323 , GRCh38.p12 chr8: 110,405,086-111,371,094 LOC107986964, LINC01608, 8 more genes
    nsv4675222copy number variation1nstd102humanPathogenic GRCh37 chr8: 111,514,791-123,192,373 , GRCh38.p12 chr8: 110,502,562-122,180,134 LOC105375723, CSMD3, 93 more genes
    nsv4672416copy number variation1nstd186human GRCh37 chr8: 111,939,993-111,944,199 , GRCh38.p12 chr8: 110,927,764-110,931,970 MTCO1P47
    nsv4670016copy number variation1nstd186human GRCh37 chr8: 111,938,018-111,944,129 , GRCh38.p12 chr8: 110,925,789-110,931,900 MTCO1P47
    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