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Items: 1 to 20 of 151

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5885163copy number variation1nstd209human GRCh38 chr1: 32,319,948-32,320,630 , GRCh37.p13 chr1: 32,785,549-32,786,231 HDAC1
    nsv5830291copy number variation1nstd209human GRCh38 chr1: 32,316,367-32,317,816 , GRCh37.p13 chr1: 32,781,968-32,783,417 HDAC1
    nsv5724953mobile element insertion1nstd211human GRCh38 chr1: 32,301,799-32,301,799 , GRCh37.p13 chr1: 32,767,400-32,767,400 HDAC1
    nsv5077559mobile element insertion1nstd203human GRCh38 chr1: 32,305,363-32,305,372 , GRCh37.p13 chr1: 32,770,964-32,770,973 HDAC1
    nsv5060222mobile element insertion1nstd203human GRCh38 chr1: 32,319,445-32,319,454 , GRCh37.p13 chr1: 32,785,046-32,785,055 HDAC1
    nsv4903325copy number variation1nstd200human GRCh38 chr1: 32,318,362-32,319,900 , GRCh37.p13 chr1: 32,783,963-32,785,501 HDAC1
    nsv4895819copy number variation1nstd200human GRCh38 chr1: 32,324,573-32,326,376 , GRCh37.p13 chr1: 32,790,174-32,791,977 HDAC1
    nsv4895818copy number variation1nstd200human GRCh38 chr1: 32,309,509-32,311,225 , GRCh37.p13 chr1: 32,775,110-32,776,826 HDAC1
    nsv4780758copy number variation1nstd200human GRCh37 chr1: 32,783,963-32,785,501 , GRCh38.p12 chr1: 32,318,362-32,319,900 HDAC1
    nsv4772967copy number variation1nstd200human GRCh37 chr1: 32,775,110-32,776,826 , GRCh38.p12 chr1: 32,309,509-32,311,225 HDAC1
    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
    nsv4454237copy number variation1nstd102humanUncertain significance GRCh37 chr1: 32,139,063-32,940,848 , GRCh38.p12 chr1: 31,673,462-32,475,247 IQCC, TSSK3, 26 more genes
    nsv4436181copy number variation1nstd102humanUncertain significance GRCh37 chr1: 10,333,430-103,467,088 , GRCh38.p12 chr1: 10,273,372-103,001,532 LINC01776, IGSF21-AS1, 1853 more genes
    nsv4048424copy number variation1nstd166human GRCh37.p13 chr1: 32,763,376-32,763,459 , GRCh38.p12 chr1: 32,297,775-32,297,858 HDAC1
    nsv4041175copy number variation1nstd166human GRCh37.p13 chr1: 32,759,226-32,766,817 , GRCh38.p12 chr1: 32,293,625-32,301,216 HDAC1
    nsv4036646copy number variation1nstd166human GRCh37.p13 chr1: 32,790,174-32,791,977 , GRCh38.p12 chr1: 32,324,573-32,326,376 HDAC1
    nsv4034475copy number variation1nstd166human GRCh37.p13 chr1: 32,786,507-32,786,820 , GRCh38.p12 chr1: 32,320,906-32,321,219 HDAC1
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