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 97

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6116137copy number variation1nstd186human GRCh37 chrX: 12,639,607-12,641,607 , GRCh38.p12 chrX: 12,621,488-12,623,488 FRMPD4
    nsv6115769copy number variation1nstd186human GRCh37 chrX: 11,953,199-11,959,435 , GRCh38.p12 chrX: 11,935,080-11,941,316 FRMPD4
    nsv6114130copy number variation1nstd186human GRCh37 chrX: 12,491,012-12,492,308 , GRCh38.p12 chrX: 12,472,893-12,474,189 FRMPD4
    nsv6112690copy number variation1nstd102humanPathogenic GRCh37 chrX: 60,000-155,234,966 , GRCh38.p12 chrX: 10,001-156,005,301 LOC105373176, ZFX-AS1, 2151 more genes
    nsv5964448insertion1nstd209human GRCh38 chrX: 11,865,033-11,865,033 , GRCh37.p13 chrX: 11,883,152-11,883,152 FRMPD4
    nsv5962158insertion1nstd209human GRCh38 chrX: 12,193,771-12,193,771 , GRCh37.p13 chrX: 12,211,890-12,211,890 FRMPD4
    nsv5951928insertion1nstd209human GRCh38 chrX: 12,559,518-12,559,518 , GRCh37.p13 chrX: 12,577,637-12,577,637 FRMPD4
    nsv5886228copy number variation1nstd209human GRCh38 chrX: 12,472,895-12,474,188 , GRCh37.p13 chrX: 12,491,014-12,492,307 FRMPD4
    nsv5880505copy number variation1nstd209human GRCh38 chrX: 12,121,026-12,121,123 , GRCh37.p13 chrX: 12,139,145-12,139,242 FRMPD4
    nsv5878207copy number variation1nstd209human GRCh38 chrX: 12,193,771-12,193,834 , GRCh37.p13 chrX: 12,211,890-12,211,953 FRMPD4
    nsv5874651copy number variation1nstd209human GRCh38 chrX: 11,935,066-11,941,315 , GRCh37.p13 chrX: 11,953,185-11,959,434 FRMPD4
    nsv5870581copy number variation1nstd209human GRCh38 chrX: 12,575,822-12,575,905 , GRCh37.p13 chrX: 12,593,941-12,594,024 FRMPD4
    nsv5867722copy number variation1nstd209human GRCh38 chrX: 12,416,131-12,418,693 , GRCh37.p13 chrX: 12,434,250-12,436,812 FRMPD4
    nsv5730351mobile element insertion1nstd211human GRCh38 chrX: 12,366,591-12,366,591 , GRCh37.p13 chrX: 12,384,710-12,384,710 FRMPD4
    nsv5730115mobile element insertion1nstd211human GRCh38 chrX: 12,547,036-12,547,036 , GRCh37.p13 chrX: 12,565,155-12,565,155 FRMPD4
    nsv5729717mobile element insertion2nstd211human GRCh38 chrX: 12,116,924-12,116,924 , GRCh37.p13 chrX: 12,135,043-12,135,043 FRMPD4
    nsv5729229mobile element insertion1nstd211human GRCh38 chrX: 12,231,836-12,231,836 , GRCh37.p13 chrX: 12,249,955-12,249,955 FRMPD4
    nsv5728667mobile element insertion1nstd211human GRCh38 chrX: 12,286,815-12,286,815 , GRCh37.p13 chrX: 12,304,934-12,304,934 FRMPD4
    nsv5727731mobile element insertion2nstd211human GRCh38 chrX: 12,015,210-12,015,210 , GRCh37.p13 chrX: 12,033,329-12,033,329 FRMPD4
    nsv5726693mobile element insertion2nstd211human GRCh38 chrX: 12,198,354-12,198,354 , GRCh37.p13 chrX: 12,216,473-12,216,473 FRMPD4
    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