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Items: 1 to 20 of 416

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7074643inversion1nstd229human GRCh38 chr12: 123,471,880-125,706,144 , GRCh37.p13 chr12: 123,956,427-126,190,690 DHX37, RNU6-927P, 44 more genes
    nsv7074199inversion1nstd229human GRCh38 chr12: 123,186,434-132,825,682 , GRCh37.p13 chr12: 123,670,981-133,402,268 PIWIL1, FZD10-AS1, 187 more genes
    nsv7069773inversion1nstd229human GRCh38 chr12: 125,029,542-125,029,595 , GRCh37.p13 chr12: 125,514,088-125,514,141 BRI3BP
    nsv6934352copy number variation1nstd229human GRCh38 chr12: 125,051,922-125,051,952 , GRCh37.p13 chr12: 125,536,468-125,536,498 BRI3BP
    nsv6933471copy number variation1nstd229human GRCh38 chr12: 125,045,505-125,047,606 , GRCh37.p13 chr12: 125,530,051-125,532,152 BRI3BP
    nsv6932515copy number variation1nstd229human GRCh38 chr12: 125,000,502-125,009,421 , GRCh37.p13 chr12: 125,485,048-125,493,967 BRI3BP
    nsv6929494copy number variation1nstd229human GRCh38 chr12: 125,041,001-125,046,500 , GRCh37.p13 chr12: 125,525,547-125,531,046 BRI3BP
    nsv6925594copy number variation1nstd229human GRCh38 chr12: 125,040,238-125,046,497 , GRCh37.p13 chr12: 125,524,784-125,531,043 BRI3BP
    nsv6921519copy number variation1nstd229human GRCh38 chr12: 125,005,530-125,010,541 , GRCh37.p13 chr12: 125,490,076-125,495,087 BRI3BP
    nsv6919854copy number variation1nstd229human GRCh38 chr12: 125,033,995-125,034,839 , GRCh37.p13 chr12: 125,518,541-125,519,385 BRI3BP
    nsv6638030copy number variation1nstd102humanUncertain significance GRCh37 chr12: 125,346,689-126,135,525 , GRCh38.p12 chr12: 124,862,143-125,650,979 MIR5188, TRD-GTC2-10, 19 more genes
    nsv6581741inversion1nstd223human GRCh38 chr12: 123,471,879-125,706,143 , GRCh37.p13 chr12: 123,956,426-126,190,689 LOC105370042, TMEM132B, 44 more genes
    nsv6580433inversion1nstd223human GRCh38 chr12: 124,997,410-124,997,845 , GRCh37.p13 chr12: 125,481,956-125,482,391 BRI3BP
    nsv6491582copy number variation1nstd223human GRCh38 chr12: 124,983,354-124,996,171 , GRCh37.p13 chr12: 125,467,900-125,480,717 DHX37, BRI3BP
    nsv6491359copy number variation1nstd223human GRCh38 chr12: 125,008,386-125,009,334 , GRCh37.p13 chr12: 125,492,932-125,493,880 BRI3BP
    nsv6488304copy number variation1nstd223human GRCh38 chr12: 124,999,801-125,002,700 , GRCh37.p13 chr12: 125,484,347-125,487,246 BRI3BP
    nsv6488089copy number variation1nstd223human GRCh38 chr12: 125,006,049-125,007,359 , GRCh37.p13 chr12: 125,490,595-125,491,905 BRI3BP
    nsv6487948copy number variation1nstd223human GRCh38 chr12: 124,993,401-124,994,800 , GRCh37.p13 chr12: 125,477,947-125,479,346 BRI3BP
    nsv6487315copy number variation1nstd223human GRCh38 chr12: 125,010,461-125,011,881 , GRCh37.p13 chr12: 125,495,007-125,496,427 BRI3BP
    nsv6482244copy number variation1nstd223human GRCh38 chr12: 124,997,301-124,999,900 , GRCh37.p13 chr12: 125,481,847-125,484,446 BRI3BP
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