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Items: 1 to 20 of 218

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5723004mobile element insertion1nstd211human GRCh38 chr10: 42,816,829-42,816,829 , GRCh37.p13 chr10: 43,312,277-43,312,277 BMS1
    nsv5644335insertion1nstd207human GRCh38 chr10: 42,834,618-42,834,618 , GRCh37.p13 chr10: 43,330,066-43,330,066 BMS1
    nsv5630985insertion1nstd207human GRCh38 chr10: 42,830,350-42,830,350 , GRCh37.p13 chr10: 43,325,798-43,325,798 BMS1
    nsv5490268copy number variation1nstd206human GRCh38 chr10: 42,827,403-42,828,417 , GRCh37.p13 chr10: 43,322,851-43,323,865 BMS1
    nsv5489882copy number variation1nstd206human GRCh38 chr10: 42,783,594-42,783,736 , GRCh37.p13 chr10: 43,279,042-43,279,184 BMS1
    nsv5474690copy number variation1nstd206human GRCh38 chr10: 42,604,677-42,829,183 , GRCh37.p13 chr10: 43,100,125-43,324,631 BMS1, LOC283028, 10 more genes
    nsv5307466copy number variation1nstd204human GRCh38.p13 chr10: 42,827,379-42,828,439 , GRCh37.p13 chr10: 43,322,827-43,323,887 BMS1
    nsv5132935mobile element insertion1nstd203human GRCh38 chr10: 42,798,309-42,798,326 , GRCh37.p13 chr10: 43,293,757-43,293,774 BMS1
    nsv5035636inversion1nstd200human GRCh38 chr10: 32,580,256-50,959,654 , GRCh37.p13 chr10: 32,869,184-52,719,414 , ZNF32-AS2, 320 more genes
    nsv5033632inversion1nstd200human GRCh38 chr10: 36,819,152-58,318,428 , GRCh37.p13 chr10: 37,108,080-60,078,188 , LOC107001062, 306 more genes
    nsv4989029copy number variation1nstd200human GRCh38 chr10: 42,103,130-42,919,644 , GRCh37.p13 chr10: 42,598,578-43,415,092 LOC105378267, BMS1, 23 more genes
    nsv4969740copy number variation1nstd200human GRCh38 chr10: 42,827,403-42,828,417 , GRCh37.p13 chr10: 43,322,851-43,323,865 BMS1
    nsv4870857inversion1nstd200human GRCh37 chr10: 37,108,081-60,078,188 , GRCh38.p12 chr10: 36,819,153-58,318,428 , NCOA4, 306 more genes
    nsv4831918copy number variation1nstd200human GRCh37 chr10: 43,322,851-43,323,865 , GRCh38.p12 chr10: 42,827,403-42,828,417 BMS1
    nsv4712787translocation1nstd195human GRCh37 chr10: 43,330,118-43,330,118 , GRCh37 chr16: 33,485,955-33,485,955 , GRCh38.p12 chr10: 42,834,670-42,834,670 , GRCh38.p12 chr16: 33,683,488-33,683,488 BMS1, BMS1P8
    nsv4711063translocation1nstd195human GRCh37 chr10: 43,330,118-43,330,118 , GRCh37 chr16: 33,485,954-33,485,954 , GRCh38.p12 chr10: 42,834,670-42,834,670 , GRCh38.p12 chr16: 33,683,487-33,683,487 BMS1, BMS1P8
    nsv4671182copy number variation1nstd186human GRCh37 chr10: 43,327,081-43,329,988 , GRCh38.p12 chr10: 42,831,633-42,834,540 BMS1, RNU6-885P
    nsv4618088copy number variation1nstd183human GRCh37 chr10: 43,316,336-43,319,234 , GRCh38.p12 chr10: 42,820,888-42,823,786 BMS1
    nsv4614777copy number variation1nstd183human GRCh37 chr10: 43,311,389-43,365,306 , GRCh38.p12 chr10: 42,815,941-42,869,858 LINC02623, RNU6-885P, 1 more genes
    nsv4610798copy number variation1nstd183human GRCh37 chr10: 43,301,539-43,355,457 , GRCh38.p12 chr10: 42,806,091-42,860,009 RNU6-885P, BMS1
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