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Items: 1 to 20 of 176

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148241copy number variation1nstd102humanPathogenic GRCh38 chr4: 79,123,548-99,457,773 , GRCh37.p13 chr4: 80,044,702-100,378,930 LOC105377327, LOC105377324, 214 more genes
    nsv7054149inversion1nstd229human GRCh38 chr4: 79,216,923-83,461,355 , GRCh37.p13 chr4: 80,138,077-84,382,508 RNU6-615P, ANTXR2, 63 more genes
    nsv7051977inversion1nstd229human GRCh38 chr4: 80,266,608-80,271,233 , GRCh37.p13 chr4: 81,187,762-81,192,387 FGF5
    nsv7049185inversion1nstd229human GRCh38 chr4: 77,808,799-83,184,403 , GRCh37.p13 chr4: 78,729,953-84,105,556 VAMP9P, HNRNPA3P13, 75 more genes
    nsv7043213inversion1nstd229human GRCh38 chr4: 80,266,274-80,275,556 , GRCh37.p13 chr4: 81,187,428-81,196,710 FGF5
    nsv7040415inversion1nstd229human GRCh38 chr4: 72,183,424-80,893,316 , GRCh37.p13 chr4: 73,049,141-81,814,470 , KPNA2P1, 148 more genes
    nsv6757068copy number variation1nstd229human GRCh38 chr4: 80,289,001-80,300,200 , GRCh37.p13 chr4: 81,210,155-81,221,354 FGF5
    nsv6753259copy number variation1nstd229human GRCh38 chr4: 80,285,434-80,341,851 , GRCh37.p13 chr4: 81,206,588-81,263,005 FGF5, CFAP299, 1 more genes
    nsv6750482copy number variation1nstd229human GRCh38 chr4: 80,172,334-80,414,520 , GRCh37.p13 chr4: 81,093,488-81,335,674 PRDM8, LOC100419739, 4 more genes
    nsv6567663inversion1nstd223human GRCh38 chr4: 80,266,608-80,271,233 , GRCh37.p13 chr4: 81,187,762-81,192,387 FGF5
    nsv6565136inversion1nstd223human GRCh38 chr4: 74,413,523-83,001,891 , GRCh37.p13 chr4: 75,279,240-83,923,044 RNU6-615P, SHROOM3, 144 more genes
    nsv6392733copy number variation1nstd223human GRCh38 chr4: 80,290,501-80,359,200 , GRCh37.p13 chr4: 81,211,655-81,280,354 MRPS25P1, FGF5, 1 more genes
    nsv6392570copy number variation1nstd223human GRCh38 chr4: 80,288,807-80,289,709 , GRCh37.p13 chr4: 81,209,961-81,210,863 FGF5
    nsv6387750copy number variation1nstd223human GRCh38 chr4: 80,272,301-80,273,600 , GRCh37.p13 chr4: 81,193,455-81,194,754 FGF5
    nsv6381470copy number variation1nstd223human GRCh38 chr4: 80,285,092-80,285,814 , GRCh37.p13 chr4: 81,206,246-81,206,968 FGF5
    nsv6379950copy number variation1nstd223human GRCh38 chr4: 80,272,716-80,273,176 , GRCh37.p13 chr4: 81,193,870-81,194,330 FGF5
    nsv6314916copy number variation1nstd102humanPathogenic GRCh38 chr4: 67,833,055-82,716,065 , GRCh37.p13 chr4: 68,698,773-83,637,218 MICOS10P4, SULT1B1, 274 more genes
    nsv6313848copy number variation1nstd102humanPathogenic GRCh37 chr4: 81,054,789-90,667,421 , GRCh38.p12 chr4: 80,133,635-89,746,270 RPL6P13, SNORD144, 136 more genes
    nsv6313633copy number variation1nstd102humanUncertain significance GRCh37 chr4: 80,865,788-82,927,188 , GRCh38.p12 chr4: 79,944,634-82,006,035 RASGEF1B, BMP3, 16 more genes
    nsv6313510copy number variation1nstd102humanPathogenic GRCh37 chr4: 75,737,340-91,131,156 , GRCh38.p12 chr4: 74,812,130-90,210,005 HIGD1AP13, CXCL11, 240 more genes
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