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Items: 1 to 20 of 199

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5971250insertion1nstd209human GRCh38 chr14: 77,372,907-77,372,907 , GRCh37.p13 chr14: 77,839,250-77,839,250 TMED8
    nsv5931678copy number variation1nstd209human GRCh38 chr14: 75,925,125-77,416,814 , GRCh37.p13 chr14: 76,391,468-77,883,157 TMED8, LOC105370573, 37 more genes
    nsv5499735copy number variation1nstd206human GRCh38 chr14: 77,349,110-77,355,197 , GRCh37.p13 chr14: 77,815,453-77,821,540 TMED8
    nsv5495105copy number variation1nstd206human GRCh38 chr14: 77,349,406-77,351,497 , GRCh37.p13 chr14: 77,815,749-77,817,840 TMED8
    nsv5342548translocation1nstd200human GRCh37 chr14: 77,835,275-77,835,275 , GRCh37 chr14: 77,832,316-77,832,316 , GRCh38.p12 chr14: 77,365,973-77,365,973 , GRCh38.p12 chr14: 77,368,932-77,368,932 TMED8
    nsv5342504translocation1nstd200human GRCh37 chr14: 77,833,925-77,833,925 , GRCh37 chr14: 77,832,403-77,832,403 , GRCh38.p12 chr14: 77,366,060-77,366,060 , GRCh38.p12 chr14: 77,367,582-77,367,582 TMED8
    nsv5329373translocation1nstd204human GRCh38.p13 chr14: 77,366,060-77,366,060 , GRCh38.p13 chr14: 77,367,582-77,367,582 , GRCh37.p13 chr14: 77,833,925-77,833,925 , GRCh37.p13 chr14: 77,832,403-77,832,403 TMED8
    nsv5323943translocation1nstd204human GRCh38.p13 chr14: 77,368,932-77,368,932 , GRCh38.p13 chr14: 77,365,973-77,365,973 , GRCh37.p13 chr14: 77,832,316-77,832,316 , GRCh37.p13 chr14: 77,835,275-77,835,275 TMED8
    nsv5309598copy number variation1nstd204human GRCh38.p13 chr14: 77,367,571-77,368,940 , GRCh37.p13 chr14: 77,833,914-77,835,283 TMED8
    nsv5198290mobile element insertion1nstd203human GRCh38 chr14: 77,338,906-77,338,919 , GRCh37.p13 chr14: 77,805,249-77,805,262 TMED8
    nsv5154749mobile element insertion1nstd203human GRCh38 chr14: 77,362,555-77,362,566 , GRCh37.p13 chr14: 77,828,898-77,828,909 TMED8
    nsv5140768mobile element insertion1nstd203human GRCh38 chr14: 77,362,549-77,362,566 , GRCh37.p13 chr14: 77,828,892-77,828,909 TMED8
    nsv5032025inversion1nstd200human GRCh38 chr14: 53,190,097-88,878,877 , GRCh37.p13 chr14: 53,656,815-89,345,221 , IFT43, 578 more genes
    nsv5000175copy number variation1nstd200human GRCh38 chr14: 77,367,575-77,368,940 , GRCh37.p13 chr14: 77,833,918-77,835,283 TMED8
    nsv5000174copy number variation1nstd200human GRCh38 chr14: 77,351,191-77,351,757 , GRCh37.p13 chr14: 77,817,534-77,818,100 TMED8
    nsv4842841copy number variation1nstd200human GRCh37 chr14: 77,817,635-77,818,803 , GRCh38.p12 chr14: 77,351,292-77,352,460 TMED8
    nsv4830656copy number variation1nstd200human GRCh37 chr14: 77,833,924-77,835,274 , GRCh38.p12 chr14: 77,367,581-77,368,931 TMED8
    nsv4671361copy number variation1nstd186human GRCh37 chr14: 77,815,467-77,817,616 , GRCh38.p12 chr14: 77,349,124-77,351,273 TMED8
    nsv4623583copy number variation1nstd183human GRCh37 chr14: 77,815,466-77,821,550 , GRCh38.p12 chr14: 77,349,123-77,355,207 TMED8
    nsv4619561copy number variation1nstd183human GRCh37 chr14: 77,815,467-77,817,616 , GRCh38.p12 chr14: 77,349,124-77,351,273 TMED8
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