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Items: 1 to 20 of 203

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5691113mobile element insertion1nstd211human GRCh38 chr1: 24,369,107-24,369,107 , GRCh37.p13 chr1: 24,695,597-24,695,597 STPG1
    nsv5686170mobile element insertion1nstd211human GRCh38 chr1: 24,389,187-24,389,187 , GRCh37.p13 chr1: 24,715,677-24,715,677 STPG1
    nsv5427686copy number variation1nstd206human GRCh38 chr1: 22,064,395-28,290,354 , GRCh37.p13 chr1: 22,390,888-28,616,865 , NCMAP-DT, 201 more genes
    nsv5427128copy number variation1nstd206human GRCh38 chr1: 24,378,052-24,378,116 , GRCh37.p13 chr1: 24,704,542-24,704,606 STPG1
    nsv5405302mobile element insertion1nstd206human GRCh38 chr1: 24,389,187-24,389,238 , GRCh37.p13 chr1: 24,715,677-24,715,728 STPG1
    nsv5403569mobile element insertion1nstd206human GRCh38 chr1: 24,369,107-24,369,158 , GRCh37.p13 chr1: 24,695,597-24,695,648 STPG1
    nsv5350125translocation1nstd200human GRCh38 chr1: 24,366,115-24,366,115 , GRCh38 chr1: 24,366,461-24,366,461 , GRCh37.p13 chr1: 24,692,951-24,692,951 , GRCh37.p13 chr1: 24,692,605-24,692,605 STPG1
    nsv5076807mobile element insertion1nstd203human GRCh38 chr1: 24,374,556-24,374,575 , GRCh37.p13 chr1: 24,701,046-24,701,065 STPG1
    nsv5065906mobile element insertion1nstd203human GRCh38 chr1: 24,395,042-24,395,058 , GRCh37.p13 chr1: 24,721,532-24,721,548 STPG1
    nsv5063831mobile element insertion1nstd203human GRCh38 chr1: 24,412,398-24,412,413 , GRCh37.p13 chr1: 24,738,888-24,738,903 STPG1, NIPAL3
    nsv5062477mobile element insertion1nstd203human GRCh38 chr1: 24,369,094-24,369,107 , GRCh37.p13 chr1: 24,695,584-24,695,597 STPG1
    nsv5060891mobile element insertion1nstd203human GRCh38 chr1: 24,383,483-24,383,497 , GRCh37.p13 chr1: 24,709,973-24,709,987 STPG1
    nsv4895388copy number variation1nstd200human GRCh38 chr1: 24,384,133-24,385,147 , GRCh37.p13 chr1: 24,710,623-24,711,637 STPG1
    nsv4895387copy number variation1nstd200human GRCh38 chr1: 24,356,044-24,376,115 , GRCh37.p13 chr1: 24,682,534-24,702,605 GRHL3, STPG1
    nsv4783130copy number variation1nstd200human GRCh37 chr1: 24,710,623-24,711,637 , GRCh38.p12 chr1: 24,384,133-24,385,147 STPG1
    nsv4767860inversion1nstd199human GRCh37 chr1: 17,051,740-234,912,187 , GRCh38.p12 chr1: 16,725,245-234,776,440 , ABCA4, 4269 more genes
    nsv4761183inversion1nstd199human GRCh37 chr1: 16,884,570-145,374,569 , GRCh38.p12 chr1: 16,558,075-149,528,945 , ABCA4, 2341 more genes
    nsv4751400inversion1nstd199human GRCh37 chr1: 17,125,657-234,919,132 , GRCh38.p12 chr1: 16,799,162-234,783,385 , ABCA4, 4264 more genes
    nsv4684226copy number variation1nstd102humanUncertain significance GRCh37 chr1: 24,394,811-25,148,686 , GRCh38.p12 chr1: 24,068,321-24,822,195 GRHL3, CLIC4, 16 more genes
    nsv4665313copy number variation1nstd186human GRCh37 chr1: 24,676,708-24,681,505 , GRCh38.p12 chr1: 24,350,218-24,355,015 GRHL3, STPG1
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