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Items: 1 to 20 of 1015

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5925821copy number variation1nstd209human GRCh38 chr8: 144,561,837-144,562,784 , GRCh37.p13 chr8: 145,787,221-145,788,168 ARHGAP39
    nsv5925474copy number variation1nstd209human GRCh38 chr8: 144,687,939-144,688,010 , GRCh37.p13 chr8: 145,913,324-145,913,395 ARHGAP39
    nsv5923519copy number variation1nstd209human GRCh38 chr8: 144,617,369-144,617,428 , GRCh37.p13 chr8: 145,842,754-145,842,813 ARHGAP39
    nsv5922650copy number variation1nstd209human GRCh38 chr8: 144,556,772-144,557,390 , GRCh37.p13 chr8: 145,782,156-145,782,774 ARHGAP39
    nsv5922460copy number variation1nstd209human GRCh38 chr8: 144,531,241-144,532,014 , GRCh37.p13 chr8: 145,756,625-145,757,398 ARHGAP39
    nsv5920534copy number variation1nstd209human GRCh38 chr8: 144,556,684-144,557,568 , GRCh37.p13 chr8: 145,782,068-145,782,952 ARHGAP39
    nsv5918695copy number variation1nstd209human GRCh38 chr8: 144,687,832-144,688,009 , GRCh37.p13 chr8: 145,913,217-145,913,394 ARHGAP39
    nsv5918297copy number variation1nstd209human GRCh38 chr8: 144,531,191-144,532,075 , GRCh37.p13 chr8: 145,756,575-145,757,459 ARHGAP39
    nsv5917184copy number variation1nstd209human GRCh38 chr8: 144,648,815-144,654,399 , GRCh37.p13 chr8: 145,874,200-145,879,784 ARHGAP39
    nsv5912265copy number variation1nstd209human GRCh38 chr8: 144,581,994-144,582,047 , GRCh37.p13 chr8: 145,807,378-145,807,431 ARHGAP39
    nsv5912047copy number variation1nstd209human GRCh38 chr8: 144,619,940-144,620,572 , GRCh37.p13 chr8: 145,845,325-145,845,957 ARHGAP39
    nsv5911613copy number variation1nstd209human GRCh38 chr8: 144,678,951-144,681,197 , GRCh37.p13 chr8: 145,904,336-145,906,582 ARHGAP39
    nsv5909671copy number variation1nstd209human GRCh38 chr8: 144,561,770-144,562,109 , GRCh37.p13 chr8: 145,787,154-145,787,493 ARHGAP39
    nsv5907822copy number variation1nstd209human GRCh38 chr8: 144,639,628-144,643,828 , GRCh37.p13 chr8: 145,865,013-145,869,213 ARHGAP39
    nsv5857638copy number variation1nstd209human GRCh38 chr8: 144,693,502-144,694,901 , GRCh37.p13 chr8: 145,918,887-145,920,286 ARHGAP39
    nsv5856992copy number variation1nstd209human GRCh38 chr8: 144,648,757-144,653,956 , GRCh37.p13 chr8: 145,874,142-145,879,341 ARHGAP39
    nsv5847633copy number variation1nstd209human GRCh38 chr8: 144,639,757-144,643,856 , GRCh37.p13 chr8: 145,865,142-145,869,241 ARHGAP39
    nsv5847591copy number variation2nstd209human GRCh38 chr8: 144,651,857-144,652,856 , GRCh37.p13 chr8: 145,877,242-145,878,241 ARHGAP39
    nsv5729039mobile element insertion1nstd211human GRCh38 chr8: 144,633,166-144,633,166 , GRCh37.p13 chr8: 145,858,551-145,858,551 ARHGAP39
    nsv5694653mobile element insertion1nstd211human GRCh38 chr8: 144,609,344-144,609,344 , GRCh37.p13 chr8: 145,834,729-145,834,729 ARHGAP39
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