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Items: 1 to 20 of 606

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7066414inversion1nstd229human GRCh38 chr14: 79,890,342-89,436,638 , GRCh37.p13 chr14: 80,356,685-89,902,982 SPATA7, RNU6ATAC28P, 82 more genes
    nsv7060344inversion1nstd229human GRCh38 chr14: 81,104,679-81,358,991 , GRCh37.p13 chr14: 81,571,023-81,825,335 STON2, LOC105370594, 8 more genes
    nsv6976410copy number variation1nstd229human GRCh38 chr14: 80,930,772-80,987,652 , GRCh37.p13 chr14: 81,397,116-81,453,996 GPRASP3P1, CEP128, 1 more genes
    nsv6976399copy number variation1nstd229human GRCh38 chr14: 81,130,709-81,131,015 , GRCh37.p13 chr14: 81,597,053-81,597,359 TSHR, LOC101928462
    nsv6976051copy number variation1nstd229human GRCh38 chr14: 81,114,001-81,144,300 , GRCh37.p13 chr14: 81,580,345-81,610,644 LOC101928462, TSHR
    nsv6974470copy number variation1nstd229human GRCh38 chr14: 81,014,021-81,021,145 , GRCh37.p13 chr14: 81,480,365-81,487,489 TSHR
    nsv6974310copy number variation1nstd229human GRCh38 chr14: 81,085,525-81,091,846 , GRCh37.p13 chr14: 81,551,869-81,558,190 TSHR, LOC101928462
    nsv6974127copy number variation1nstd229human GRCh38 chr14: 81,126,171-81,126,494 , GRCh37.p13 chr14: 81,592,515-81,592,838 TSHR, LOC101928462
    nsv6972207copy number variation1nstd229human GRCh38 chr14: 80,955,950-81,151,999 , GRCh37.p13 chr14: 81,422,294-81,618,343 TSHR, GPRASP3P1, 4 more genes
    nsv6969638copy number variation1nstd229human GRCh38 chr14: 81,019,132-81,028,033 , GRCh37.p13 chr14: 81,485,476-81,494,377 TSHR
    nsv6969170copy number variation1nstd229human GRCh38 chr14: 81,139,507-81,139,560 , GRCh37.p13 chr14: 81,605,851-81,605,904 TSHR, LOC101928462
    nsv6968918copy number variation1nstd229human GRCh38 chr14: 81,067,491-81,070,874 , GRCh37.p13 chr14: 81,533,835-81,537,218 LOC101928462, TSHR
    nsv6967358copy number variation1nstd229human GRCh38 chr14: 80,977,869-80,977,970 , GRCh37.p13 chr14: 81,444,213-81,444,314 TSHR
    nsv6967296copy number variation1nstd229human GRCh38 chr14: 80,954,965-81,042,155 , GRCh37.p13 chr14: 81,421,309-81,508,499 NMNAT1P1, TSHR, 3 more genes
    nsv6965795copy number variation1nstd229human GRCh38 chr14: 81,131,941-81,132,022 , GRCh37.p13 chr14: 81,598,285-81,598,366 TSHR, LOC101928462
    nsv6965306copy number variation1nstd229human GRCh38 chr14: 81,077,998-81,078,053 , GRCh37.p13 chr14: 81,544,342-81,544,397 TSHR, LOC101928462
    nsv6965219copy number variation1nstd229human GRCh38 chr14: 81,128,363-81,135,243 , GRCh37.p13 chr14: 81,594,707-81,601,587 TSHR, LOC101928462
    nsv6965113copy number variation1nstd229human GRCh38 chr14: 81,142,039-81,146,933 , GRCh37.p13 chr14: 81,608,383-81,613,277 LOC101928462, TSHR
    nsv6962968copy number variation1nstd229human GRCh38 chr14: 81,024,285-81,024,559 , GRCh37.p13 chr14: 81,490,629-81,490,903 TSHR
    nsv6962621copy number variation1nstd229human GRCh38 chr14: 80,829,329-81,073,652 , GRCh37.p13 chr14: 81,295,673-81,539,996 NMNAT1P1, LOC101928462, 4 more genes
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