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Items: 1 to 20 of 144

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7042877inversion1nstd229human GRCh38 chr6: 149,723,719-152,206,487 , GRCh37.p13 chr6: 150,044,855-152,527,622 MTHFD1L, RAET1F, 48 more genes
    nsv6816460copy number variation1nstd229human GRCh38 chr6: 149,732,825-149,736,258 , GRCh37.p13 chr6: 150,053,961-150,057,394 NUP43
    nsv6609768copy number variation1nstd223human GRCh38 chr6: 149,732,301-149,736,300 , GRCh37.p13 chr6: 150,053,437-150,057,436 NUP43
    nsv6575285inversion1nstd223human GRCh38 chr6: 149,721,980-149,723,256 , GRCh37.p13 chr6: 150,043,116-150,044,392 NUP43
    nsv6571422inversion1nstd223human GRCh38 chr6: 146,996,555-151,115,323 , GRCh37.p13 chr6: 147,317,691-151,436,459 RPSAP40, STXBP5, 62 more genes
    nsv6568519inversion1nstd223human GRCh38 chr6: 149,742,073-149,742,942 , GRCh37.p13 chr6: 150,063,209-150,064,078 NUP43
    nsv6565625inversion1nstd223human GRCh38 chr6: 149,740,579-149,741,284 , GRCh37.p13 chr6: 150,061,715-150,062,420 NUP43
    nsv6558955inversion1nstd223human GRCh38 chr6: 149,732,022-149,733,517 , GRCh37.p13 chr6: 150,053,158-150,054,653 NUP43
    nsv6141175copy number variation1nstd206human GRCh38 chr6: 149,732,825-149,736,325 , GRCh37.p13 chr6: 150,053,961-150,057,461 NUP43
    nsv5897462copy number variation1nstd209human GRCh38 chr6: 149,732,806-149,736,237 , GRCh37.p13 chr6: 150,053,942-150,057,373 NUP43
    nsv5844746copy number variation1nstd209human GRCh38 chr6: 149,732,789-149,735,315 , GRCh37.p13 chr6: 150,053,925-150,056,451 NUP43
    nsv5844122copy number variation1nstd209human GRCh38 chr6: 149,732,389-149,734,715 , GRCh37.p13 chr6: 150,053,525-150,055,851 NUP43
    nsv5472467copy number variation1nstd206human GRCh38 chr6: 149,741,241-149,741,928 , GRCh37.p13 chr6: 150,062,377-150,063,064 NUP43
    nsv5466489copy number variation1nstd206human GRCh38 chr6: 149,725,575-149,730,434 , GRCh37.p13 chr6: 150,046,711-150,051,570 NUP43
    nsv5369906translocation1nstd200human GRCh38 chr6: 149,732,825-149,732,825 , GRCh38 chr6: 149,736,238-149,736,238 , GRCh37.p13 chr6: 150,057,374-150,057,374 , GRCh37.p13 chr6: 150,053,961-150,053,961 NUP43
    nsv5238088copy number variation1nstd204human GRCh38.p13 chr6: 149,592,201-149,809,100 , GRCh37.p13 chr6: 149,913,337-150,130,236 , GINM1, 8 more genes
    nsv5186543mobile element insertion1nstd203human GRCh38 chr6: 149,735,975-149,735,989 , GRCh37.p13 chr6: 150,057,111-150,057,125 NUP43
    nsv4945830copy number variation1nstd200human GRCh38 chr6: 149,737,018-149,744,607 , GRCh37.p13 chr6: 150,058,154-150,065,743 NUP43
    nsv4943348copy number variation1nstd200human GRCh38 chr6: 149,735,858-149,736,009 , GRCh37.p13 chr6: 150,056,994-150,057,145 NUP43
    nsv4810868copy number variation1nstd200human GRCh37 chr6: 150,053,961-150,057,374 , GRCh38.p12 chr6: 149,732,825-149,736,238 NUP43
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