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 1763

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137077copy number variation1nstd102humanPathogenic GRCh37 chrX: 6,968,337-8,434,424 , GRCh38.p12 chrX: 7,050,296-8,466,383 PUDP, PNPLA4, 8 more genes
    nsv7137063copy number variation1nstd102humanPathogenic GRCh37 chrX: 200,855-155,240,074 , GRCh38.p12 chrX: 284,188-156,010,409 RN7SL581P, HMGB1P32, 2151 more genes
    nsv7098913copy number variation1nstd102humanUncertain significance GRCh38 chrX: 7,873,079-8,504,515 , GRCh37.p13 chrX: 7,841,120-8,472,556 MIR651, VCX3B, 5 more genes
    nsv7098871copy number variation1nstd102humanPathogenic GRCh37 chrX: 6,451,786-7,894,160 , GRCh38.p12 chrX: 6,533,745-7,926,119 STS, PUDP, 7 more genes
    nsv7077760copy number variation1nstd229human GRCh38 chrX: 8,218,837-8,219,484 , GRCh37.p13 chrX: 8,186,878-8,187,525 LOC107985675
    nsv7077512copy number variation1nstd229human GRCh38 chrX: 7,371,659-7,960,351 , GRCh37.p13 chrX: 7,289,700-7,928,392 PNPLA4, LOC107985675, 1 more genes
    nsv7077097copy number variation1nstd229human GRCh38 chrX: 7,962,439-8,605,914 , GRCh37.p13 chrX: 7,930,480-8,573,955 VCX2, LOC107985676, 5 more genes
    nsv7076962copy number variation1nstd229human GRCh38 chrX: 8,445,099-8,830,475 , GRCh37.p13 chrX: 8,413,140-8,798,516 FAM9A, LOC107985675, 4 more genes
    nsv7076816copy number variation1nstd229human GRCh38 chrX: 8,093,045-8,125,435 , GRCh37.p13 chrX: 8,061,086-8,093,476 LOC107985675, MIR651
    nsv7076586copy number variation1nstd229human GRCh38 chrX: 8,348,168-8,355,980 , GRCh37.p13 chrX: 8,316,209-8,324,021 LOC107985675
    nsv7076532copy number variation1nstd229human GRCh38 chrX: 8,232,801-8,242,900 , GRCh37.p13 chrX: 8,200,842-8,210,941 LOC107985675
    nsv7076371copy number variation1nstd229human GRCh38 chrX: 8,208,101-8,210,900 , GRCh37.p13 chrX: 8,176,142-8,178,941 LOC107985675
    nsv7075968copy number variation1nstd229human GRCh38 chrX: 8,398,693-8,412,002 , GRCh37.p13 chrX: 8,366,734-8,380,043 LOC107985675
    nsv7075765copy number variation1nstd229human GRCh38 chrX: 8,209,927-8,210,732 , GRCh37.p13 chrX: 8,177,968-8,178,773 LOC107985675
    nsv7075764copy number variation1nstd229human GRCh38 chrX: 7,881,915-8,050,791 , GRCh37.p13 chrX: 7,849,956-8,018,832 LOC107985675, PNPLA4
    nsv7075663copy number variation1nstd229human GRCh38 chrX: 8,012,793-8,016,711 , GRCh37.p13 chrX: 7,980,834-7,984,752 LOC107985675
    nsv7075451copy number variation1nstd229human GRCh38 chrX: 8,156,773-8,167,008 , GRCh37.p13 chrX: 8,124,814-8,135,049 LOC107985675
    nsv7075180copy number variation1nstd229human GRCh38 chrX: 8,191,801-8,220,000 , GRCh37.p13 chrX: 8,159,842-8,188,041 LOC107985675
    nsv7075113copy number variation1nstd229human GRCh38 chrX: 8,061,990-8,062,033 , GRCh37.p13 chrX: 8,030,031-8,030,074 LOC107985675
    nsv7075028copy number variation1nstd229human GRCh38 chrX: 7,472,108-8,003,905 , GRCh37.p13 chrX: 7,390,149-7,971,946 LOC107985675, VCX, 1 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