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Items: 1 to 20 of 390

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7098859copy number variation1nstd102humanUncertain significance GRCh37 chr4: 169,669,584-172,013,457 , GRCh38.p12 chr4: 168,748,433-171,092,306 RNY4P17, LOC105377529, 27 more genes
    nsv7056217inversion1nstd229human GRCh38 chr4: 166,607,935-172,500,612 , GRCh37.p13 chr4: 167,529,086-173,421,763 DDX60, LOC105377529, 50 more genes
    nsv7054944inversion1nstd229human GRCh38 chr4: 169,647,111-171,933,053 , GRCh37.p13 chr4: 170,568,262-172,854,204 PTGES3P3, LOC402192, 23 more genes
    nsv7042989inversion1nstd229human GRCh38 chr4: 169,933,182-169,934,145 , GRCh37.p13 chr4: 170,854,333-170,855,296 LOC105377530, LINC02275
    nsv7041914inversion1nstd229human GRCh38 chr4: 169,919,598-169,919,713 , GRCh37.p13 chr4: 170,840,749-170,840,864 LINC02275, LOC105377530
    nsv6756593copy number variation1nstd229human GRCh38 chr4: 169,921,201-169,925,000 , GRCh37.p13 chr4: 170,842,352-170,846,151 LINC02275, LOC105377530
    nsv6754173copy number variation1nstd229human GRCh38 chr4: 169,732,023-170,107,311 , GRCh37.p13 chr4: 170,653,174-171,028,462 PTGES3P3, LOC402192, 8 more genes
    nsv6752703copy number variation1nstd229human GRCh38 chr4: 169,946,666-169,950,675 , GRCh37.p13 chr4: 170,867,817-170,871,826 LINC02275
    nsv6752182copy number variation1nstd229human GRCh38 chr4: 169,907,275-169,917,223 , GRCh37.p13 chr4: 170,828,426-170,838,374 LOC105377530, LINC02275
    nsv6752018copy number variation1nstd229human GRCh38 chr4: 169,951,026-169,958,051 , GRCh37.p13 chr4: 170,872,177-170,879,202 LINC02275
    nsv6751581copy number variation1nstd229human GRCh38 chr4: 169,929,962-169,940,484 , GRCh37.p13 chr4: 170,851,113-170,861,635 LINC02275, LOC105377530
    nsv6750977copy number variation1nstd229human GRCh38 chr4: 169,951,923-169,958,817 , GRCh37.p13 chr4: 170,873,074-170,879,968 LINC02275
    nsv6748875copy number variation1nstd229human GRCh38 chr4: 169,944,924-169,953,416 , GRCh37.p13 chr4: 170,866,075-170,874,567 LINC02275
    nsv6747869copy number variation1nstd229human GRCh38 chr4: 169,923,980-170,085,263 , GRCh37.p13 chr4: 170,845,131-171,006,414 AADAT, LOC105377530, 3 more genes
    nsv6745993copy number variation1nstd229human GRCh38 chr4: 169,968,904-169,974,714 , GRCh37.p13 chr4: 170,890,055-170,895,865 LINC02275
    nsv6743893copy number variation1nstd229human GRCh38 chr4: 169,924,532-169,929,038 , GRCh37.p13 chr4: 170,845,683-170,850,189 LINC02275, LOC105377530
    nsv6743834copy number variation1nstd229human GRCh38 chr4: 169,949,228-169,952,451 , GRCh37.p13 chr4: 170,870,379-170,873,602 LINC02275
    nsv6741913copy number variation1nstd229human GRCh38 chr4: 169,919,150-169,921,203 , GRCh37.p13 chr4: 170,840,301-170,842,354 LINC02275, LOC105377530
    nsv6741785copy number variation1nstd229human GRCh38 chr4: 169,936,966-169,948,848 , GRCh37.p13 chr4: 170,858,117-170,869,999 LINC02275, LOC105377530
    nsv6740415copy number variation1nstd229human GRCh38 chr4: 169,956,527-169,969,209 , GRCh37.p13 chr4: 170,877,678-170,890,360 LINC02275
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