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Items: 1 to 20 of 238

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5977770insertion1nstd209human GRCh38 chr14: 96,340,148-96,340,148 , GRCh37.p13 chr14: 96,806,485-96,806,485 ATG2B
    nsv5968573insertion1nstd209human GRCh38 chr14: 96,304,995-96,304,995 , GRCh37.p13 chr14: 96,771,332-96,771,332 ATG2B
    nsv5713134mobile element insertion2nstd211human GRCh38 chr14: 96,306,599-96,306,599 , GRCh37.p13 chr14: 96,772,936-96,772,936 ATG2B
    nsv5707553mobile element insertion2nstd211human GRCh38 chr14: 96,305,006-96,305,006 , GRCh37.p13 chr14: 96,771,343-96,771,343 ATG2B
    nsv5661745insertion1nstd207human GRCh38 chr14: 96,340,148-96,340,148 , GRCh37.p13 chr14: 96,806,485-96,806,485 ATG2B
    nsv5658006insertion1nstd207human GRCh38 chr14: 96,340,103-96,340,103 , GRCh37.p13 chr14: 96,806,440-96,806,440 ATG2B
    nsv5604177copy number variation1nstd207human GRCh38 chr14: 96,308,197-96,308,254 , GRCh37.p13 chr14: 96,774,534-96,774,591 ATG2B
    nsv5504547copy number variation1nstd206human GRCh38 chr14: 96,308,024-96,308,117 , GRCh37.p13 chr14: 96,774,361-96,774,454 ATG2B
    nsv5498590copy number variation1nstd206human GRCh38 chr14: 80,522,636-106,763,637 , GRCh37.p13 chr14: 80,988,980-106,929,356 , RPS18P2, 713 more genes
    nsv5428423mobile element insertion1nstd206human GRCh38 chr14: 96,306,599-96,306,650 , GRCh37.p13 chr14: 96,772,936-96,772,987 ATG2B
    nsv5427002mobile element insertion1nstd206human GRCh38 chr14: 96,305,006-96,305,057 , GRCh37.p13 chr14: 96,771,343-96,771,394 ATG2B
    nsv5154475mobile element insertion1nstd203human GRCh38 chr14: 96,306,588-96,306,599 , GRCh37.p13 chr14: 96,772,925-96,772,936 ATG2B
    nsv5152141mobile element insertion1nstd203human GRCh38 chr14: 96,354,259-96,354,270 , GRCh37.p13 chr14: 96,820,596-96,820,607 ATG2B
    nsv5141965mobile element insertion1nstd203human GRCh38 chr14: 96,313,421-96,313,434 , GRCh37.p13 chr14: 96,779,758-96,779,771 ATG2B
    nsv5141936mobile element insertion1nstd203human GRCh38 chr14: 96,304,995-96,305,006 , GRCh37.p13 chr14: 96,771,332-96,771,343 ATG2B
    nsv5140341mobile element insertion1nstd203human GRCh38 chr14: 96,341,464-96,341,476 , GRCh37.p13 chr14: 96,807,801-96,807,813 ATG2B
    nsv5007442copy number variation1nstd200human GRCh38 chr14: 96,312,561-96,312,719 , GRCh37.p13 chr14: 96,778,898-96,779,056 ATG2B
    nsv4754932insertion1nstd199human GRCh37 chr14: 96,806,435-96,806,435 , GRCh38.p12 chr14: 96,340,098-96,340,098 ATG2B
    nsv4751432insertion1nstd199human GRCh37 chr14: 96,771,335-96,771,335 , GRCh38.p12 chr14: 96,304,998-96,304,998 ATG2B
    nsv4734792copy number variation1nstd199human GRCh37 chr14: 96,774,497-96,774,558 , GRCh38.p12 chr14: 96,308,160-96,308,221 ATG2B
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