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Items: 1 to 20 of 295

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5979667inversion1nstd209human GRCh38 chr13: 24,646,334-25,024,564 , GRCh37.p13 chr13: 25,220,472-25,598,702 , ATP12A, 14 more genes
    nsv5943160copy number variation1nstd209human GRCh38 chr13: 24,696,424-24,696,759 , GRCh37.p13 chr13: 25,270,562-25,270,897 ATP12A
    nsv5937357copy number variation1nstd209human GRCh38 chr13: 24,558,458-24,762,880 , GRCh37.p13 chr13: 25,132,596-25,337,018 , ANKRD20A10P, 11 more genes
    nsv5930119copy number variation1nstd209human GRCh38 chr13: 19,425,704-24,953,999 , GRCh37.p13 chr13: 19,999,844-25,528,137 , LOC105370102, 128 more genes
    nsv5863458copy number variation1nstd209human GRCh38 chr13: 24,677,353-24,684,690 , GRCh37.p13 chr13: 25,251,491-25,258,828 ATP12A
    nsv5861735copy number variation1nstd209human GRCh38 chr13: 24,623,494-24,690,893 , GRCh37.p13 chr13: 25,197,632-25,265,031 ATP12A
    nsv5604293copy number variation1nstd207human GRCh38 chr13: 24,696,421-24,696,756 , GRCh37.p13 chr13: 25,270,559-25,270,894 ATP12A
    nsv5597337copy number variation1nstd207human GRCh38 chr13: 24,703,832-24,703,988 , GRCh37.p13 chr13: 25,277,970-25,278,126 ATP12A, RPL26P34, 1 more genes
    nsv5564510copy number variation1nstd102humanPathogenic GRCh37 chr13: 19,053,605-115,108,528 , GRCh38.p12 chr13: 18,479,465-114,343,053 RN7SL272P, DIAPH3, 1333 more genes
    nsv5561491sequence alteration1nstd206human GRCh38 chr13: 24,595,804-24,953,333 , GRCh37.p13 chr13: 25,169,942-25,527,471 , ATP12A, 13 more genes
    nsv5510970copy number variation1nstd206human GRCh38 chr13: 24,696,424-24,696,745 , GRCh37.p13 chr13: 25,270,562-25,270,883 ATP12A
    nsv5505995copy number variation1nstd206human GRCh38 chr13: 24,673,864-24,678,939 , GRCh37.p13 chr13: 25,248,002-25,253,077 ATP12A
    nsv5382579mobile element deletion2nstd186human GRCh37 chr13: 25,270,562-25,270,883 , GRCh38.p12 chr13: 24,696,424-24,696,745 ATP12A
    nsv5379813translocation1nstd200human GRCh38 chr13: 24,695,492-24,695,492 , GRCh38 chr13: 24,760,603-24,760,603 , GRCh37.p13 chr13: 25,269,630-25,269,630 , GRCh37.p13 chr13: 25,334,741-25,334,741 ATP12A, RNF17
    nsv5209835mobile element deletion1nstd204human GRCh38.p13 chr13: 24,696,424-24,696,745 , GRCh37.p13 chr13: 25,270,562-25,270,883 ATP12A
    nsv5187813mobile element insertion1nstd203human GRCh38 chr13: 24,711,977-24,711,992 , GRCh37.p13 chr13: 25,286,115-25,286,130 ATP12A
    nsv5004412copy number variation1nstd200human GRCh38 chr13: 24,675,798-25,035,888 , GRCh37.p13 chr13: 25,249,936-25,610,026 , TPTE2P1, 15 more genes
    nsv5004410copy number variation1nstd200human GRCh38 chr13: 24,558,458-24,762,885 , GRCh37.p13 chr13: 25,132,596-25,337,023 , LOC105370118, 11 more genes
    nsv4996617copy number variation1nstd200human GRCh38 chr13: 24,673,833-24,678,963 , GRCh37.p13 chr13: 25,247,971-25,253,101 ATP12A
    nsv4899863mobile element deletion1nstd200human GRCh38 chr13: 24,696,424-24,696,745 , GRCh37.p13 chr13: 25,270,562-25,270,883 ATP12A
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