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Items: 1 to 20 of 115

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7099193copy number variation1nstd231human GRCh38.p12 chr1: 32,456,017-38,905,781 , GRCh37 chr1: 32,921,618-39,371,453 AK2, COL8A2, 151 more genes
    nsv7054626inversion1nstd229human GRCh38 chr1: 32,864,974-32,873,844 , GRCh37.p13 chr1: 33,330,575-33,339,445 LOC105378631, FNDC5
    nsv7052999inversion1nstd229human GRCh38 chr1: 32,862,696-32,862,766 , GRCh37.p13 chr1: 33,328,297-33,328,367 FNDC5
    nsv7052945inversion1nstd229human GRCh38 chr1: 32,871,997-32,872,126 , GRCh37.p13 chr1: 33,337,598-33,337,727 FNDC5
    nsv7046389inversion1nstd229human GRCh38 chr1: 31,492,639-36,569,102 , GRCh37.p13 chr1: 32,017,064-37,034,703 LOC105378642, TMEM35B, 127 more genes
    nsv7044103inversion1nstd229human GRCh38 chr1: 26,905,652-33,050,814 , GRCh37.p13 chr1: 27,232,143-33,516,415 ADGRB2, SNORA16A, 169 more genes
    nsv6648911copy number variation1nstd229human GRCh38 chr1: 32,866,942-32,880,130 , GRCh37.p13 chr1: 33,332,543-33,345,731 LOC105378631, FNDC5
    nsv6648490copy number variation1nstd229human GRCh38 chr1: 32,872,888-32,872,917 , GRCh37.p13 chr1: 33,338,489-33,338,518 FNDC5
    nsv6333807copy number variation1nstd223human GRCh38 chr1: 32,866,942-32,880,130 , GRCh37.p13 chr1: 33,332,543-33,345,731 LOC105378631, FNDC5
    nsv6313688copy number variation1nstd102humanPathogenic GRCh37 chr1: 33,285,582-47,891,811 , GRCh38.p12 chr1: 32,819,981-47,426,139 LOC107984940, PPIAP36, 407 more genes
    nsv5869931copy number variation1nstd209human GRCh38 chr1: 32,865,248-32,865,381 , GRCh37.p13 chr1: 33,330,849-33,330,982 FNDC5
    nsv5685727mobile element insertion2nstd211human GRCh38 chr1: 32,867,502-32,867,502 , GRCh37.p13 chr1: 33,333,103-33,333,103 FNDC5
    nsv5427522copy number variation1nstd206human GRCh38 chr1: 32,870,813-32,870,930 , GRCh37.p13 chr1: 33,336,414-33,336,531 FNDC5
    nsv5416871copy number variation1nstd206human GRCh38 chr1: 32,871,376-32,871,474 , GRCh37.p13 chr1: 33,336,977-33,337,075 FNDC5
    nsv5412457mobile element insertion1nstd206human GRCh38 chr1: 32,867,502-32,867,553 , GRCh37.p13 chr1: 33,333,103-33,333,154 FNDC5
    nsv4895853copy number variation1nstd200human GRCh38 chr1: 32,865,538-32,865,648 , GRCh37.p13 chr1: 33,331,139-33,331,249 FNDC5
    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
    nsv4674454copy number variation1nstd102humanLikely pathogenic GRCh37 chr1: 30,819,875-34,380,419 , GRCh38.p12 chr1: 30,347,028-33,914,818 AK2, ADGRB2, 97 more genes
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