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Items: 1 to 20 of 191

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7066646inversion1nstd229human GRCh38 chr12: 118,044,064-118,048,006 , GRCh37.p13 chr12: 118,481,869-118,485,811 WSB2
    nsv6938018copy number variation1nstd229human GRCh38 chr12: 118,057,301-118,138,700 , GRCh37.p13 chr12: 118,495,106-118,576,505 LOC101928274, VSIG10, 2 more genes
    nsv6931149copy number variation1nstd229human GRCh38 chr12: 118,054,101-118,059,000 , GRCh37.p13 chr12: 118,491,906-118,496,805 WSB2
    nsv6929634copy number variation1nstd229human GRCh38 chr12: 118,056,707-118,060,261 , GRCh37.p13 chr12: 118,494,512-118,498,066 WSB2
    nsv6926232copy number variation1nstd229human GRCh38 chr12: 118,039,601-118,059,000 , GRCh37.p13 chr12: 118,477,406-118,496,805 WSB2
    nsv6926141copy number variation1nstd229human GRCh38 chr12: 117,966,883-118,055,344 , GRCh37.p13 chr12: 118,404,688-118,493,149 WSB2, KSR2, 1 more genes
    nsv6922916copy number variation1nstd229human GRCh38 chr12: 118,043,869-118,044,262 , GRCh37.p13 chr12: 118,481,674-118,482,067 WSB2
    nsv6583876inversion1nstd223human GRCh38 chr12: 118,054,469-123,705,974 , GRCh37.p13 chr12: 118,492,274-124,190,521 RPL11P5, RPL17P37, 159 more genes
    nsv6580031inversion1nstd223human GRCh38 chr12: 118,046,308-118,046,782 , GRCh37.p13 chr12: 118,484,113-118,484,587 WSB2
    nsv6290239copy number variation1nstd102humanLikely pathogenic GRCh37 chr12: 117,461,902-133,841,395 , GRCh38.p12 chr12: 117,024,097-133,264,809 ACADS, BCL7A, 356 more genes
    nsv6289607insertion1nstd214human GRCh38 chr12: 118,041,633-118,041,633 , GRCh37.p13 chr12: 118,479,438-118,479,438 WSB2
    nsv6132216copy number variation1nstd213human GRCh37 chr12: 117,580,000-118,570,001 , GRCh38.p12 chr12: 117,142,195-118,132,196 RFC5, KSR2, 8 more genes
    nsv5973346inversion1nstd209human GRCh38 chr12: 118,054,601-123,705,841 , GRCh37.p13 chr12: 118,492,406-124,190,388 , ACADS, 162 more genes
    nsv5941397copy number variation1nstd209human GRCh38 chr12: 118,041,605-118,041,656 , GRCh37.p13 chr12: 118,479,410-118,479,461 WSB2
    nsv5862818copy number variation1nstd209human GRCh38 chr12: 118,055,668-118,056,667 , GRCh37.p13 chr12: 118,493,473-118,494,472 WSB2
    nsv5724757mobile element insertion1nstd211human GRCh38 chr12: 118,032,093-118,032,093 , GRCh37.p13 chr12: 118,469,898-118,469,898 RFC5, WSB2
    nsv5505997copy number variation1nstd206human GRCh38 chr12: 118,048,438-118,056,705 , GRCh37.p13 chr12: 118,486,243-118,494,510 WSB2
    nsv5500677copy number variation1nstd206human GRCh38 chr12: 118,056,707-118,060,258 , GRCh37.p13 chr12: 118,494,512-118,498,063 WSB2
    nsv5356443translocation1nstd200human GRCh38 chr12: 118,034,629-118,034,629 , GRCh38 chr12: 118,034,564-118,034,564 , GRCh37.p13 chr12: 118,472,434-118,472,434 , GRCh37.p13 chr12: 118,472,369-118,472,369 WSB2
    nsv5133017mobile element insertion1nstd203human GRCh38 chr12: 118,034,922-118,034,937 , GRCh37.p13 chr12: 118,472,727-118,472,742 WSB2
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