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Items: 1 to 20 of 583

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5980227insertion1nstd209human GRCh38 chr12: 24,887,081-24,887,081 , GRCh37.p13 chr12: 25,040,015-25,040,015 BCAT1
    nsv5977028insertion1nstd209human GRCh38 chr12: 24,837,146-24,837,146 , GRCh37.p13 chr12: 24,990,080-24,990,080 BCAT1
    nsv5924990copy number variation1nstd209human GRCh38 chr12: 24,910,171-24,910,900 , GRCh37.p13 chr12: 25,063,105-25,063,834 BCAT1
    nsv5923742copy number variation1nstd209human GRCh38 chr12: 21,398,810-28,763,815 , GRCh37.p13 chr12: 21,551,744-28,916,748 , LOC105369710, 101 more genes
    nsv5922790copy number variation1nstd209human GRCh38 chr12: 24,889,970-24,891,298 , GRCh37.p13 chr12: 25,042,904-25,044,232 BCAT1
    nsv5916901copy number variation1nstd209human GRCh38 chr12: 21,398,719-28,763,765 , GRCh37.p13 chr12: 21,551,653-28,916,698 , LOC105369704, 101 more genes
    nsv5916252copy number variation1nstd209human GRCh38 chr12: 24,811,803-24,811,898 , GRCh37.p13 chr12: 24,964,737-24,964,832 BCAT1
    nsv5916198copy number variation1nstd209human GRCh38 chr12: 24,857,320-24,863,832 , GRCh37.p13 chr12: 25,010,254-25,016,766 BCAT1
    nsv5866375copy number variation1nstd209human GRCh38 chr12: 24,895,535-24,897,572 , GRCh37.p13 chr12: 25,048,469-25,050,506 BCAT1
    nsv5860622copy number variation1nstd209human GRCh38 chr12: 24,874,012-24,876,336 , GRCh37.p13 chr12: 25,026,946-25,029,270 BCAT1
    nsv5859423copy number variation1nstd209human GRCh38 chr12: 24,859,558-24,861,557 , GRCh37.p13 chr12: 25,012,492-25,014,491 BCAT1
    nsv5857073copy number variation1nstd209human GRCh38 chr12: 24,914,558-24,916,840 , GRCh37.p13 chr12: 25,067,492-25,069,774 DAD1P1, BCAT1
    nsv5854173copy number variation1nstd209human GRCh38 chr12: 24,850,097-24,852,196 , GRCh37.p13 chr12: 25,003,031-25,005,130 BCAT1
    nsv5853966copy number variation2nstd209human GRCh38 chr12: 24,889,997-24,891,346 , GRCh37.p13 chr12: 25,042,931-25,044,280 BCAT1
    nsv5853044copy number variation1nstd209human GRCh38 chr12: 24,906,433-24,909,132 , GRCh37.p13 chr12: 25,059,367-25,062,066 BCAT1
    nsv5709923mobile element insertion2nstd211human GRCh38 chr12: 24,837,061-24,837,061 , GRCh37.p13 chr12: 24,989,995-24,989,995 BCAT1
    nsv5709707mobile element insertion2nstd211human GRCh38 chr12: 24,877,017-24,877,017 , GRCh37.p13 chr12: 25,029,951-25,029,951 BCAT1
    nsv5702790mobile element insertion2nstd211human GRCh38 chr12: 24,920,012-24,920,012 , GRCh37.p13 chr12: 25,072,946-25,072,946 BCAT1
    nsv5694677mobile element insertion2nstd211human GRCh38 chr12: 24,896,895-24,896,895 , GRCh37.p13 chr12: 25,049,829-25,049,829 BCAT1
    nsv5659343insertion1nstd207human GRCh38 chr12: 24,837,146-24,837,146 , GRCh37.p13 chr12: 24,990,080-24,990,080 BCAT1
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