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Items: 1 to 20 of 1600

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7078077inversion1nstd229human GRCh38 chr8: 50,988,804-51,638,131 , GRCh37.p13 chr8: 51,901,364-52,550,691 LOC105375831, PXDNL, 1 more genes
    nsv7074880inversion1nstd229human GRCh38 chr8: 51,727,317-51,730,197 , GRCh37.p13 chr8: 52,639,877-52,642,757 PXDNL
    nsv7074554inversion1nstd229human GRCh38 chr8: 51,106,732-53,057,419 , GRCh37.p13 chr8: 52,019,292-53,969,979 LOC105375835, RPL34P17, 14 more genes
    nsv7074175inversion1nstd229human GRCh38 chr8: 51,636,484-52,045,051 , GRCh37.p13 chr8: 52,549,044-52,957,611 BTF3P1, PXDNL, 3 more genes
    nsv7074141inversion1nstd229human GRCh38 chr8: 48,828,025-51,794,653 , GRCh37.p13 chr8: 49,740,584-52,707,213 CYCSP22, LOC100422267, 19 more genes
    nsv7074060inversion1nstd229human GRCh38 chr8: 51,672,076-51,831,222 , GRCh37.p13 chr8: 52,584,636-52,743,782 BTF3P1, PXDNL, 2 more genes
    nsv7073122inversion1nstd229human GRCh38 chr8: 51,471,587-51,471,654 , GRCh37.p13 chr8: 52,384,147-52,384,214 PXDNL
    nsv7072399inversion1nstd229human GRCh38 chr8: 51,319,783-51,322,607 , GRCh37.p13 chr8: 52,232,343-52,235,167 PXDNL
    nsv7072090inversion1nstd229human GRCh38 chr8: 51,787,221-51,787,297 , GRCh37.p13 chr8: 52,699,781-52,699,857 PXDNL
    nsv7069832inversion1nstd229human GRCh38 chr8: 51,807,200-51,811,368 , GRCh37.p13 chr8: 52,719,760-52,723,928 PXDNL
    nsv7068957inversion1nstd229human GRCh38 chr8: 51,375,840-51,716,908 , GRCh37.p13 chr8: 52,288,400-52,629,468 BRIX1P1, PXDNL
    nsv7067508inversion1nstd229human GRCh38 chr8: 51,755,366-56,976,322 , GRCh37.p13 chr8: 52,667,926-57,888,881 CHCHD2P10, LOC105375850, 81 more genes
    nsv7067487inversion1nstd229human GRCh38 chr8: 51,760,382-51,766,564 , GRCh37.p13 chr8: 52,672,942-52,679,124 LOC105375833, PXDNL
    nsv7065573inversion1nstd229human GRCh38 chr8: 50,010,746-51,804,722 , GRCh37.p13 chr8: 50,923,306-52,717,282 LOC105375830, LOC100422267, 10 more genes
    nsv7064780inversion1nstd229human GRCh38 chr8: 51,801,390-51,811,475 , GRCh37.p13 chr8: 52,713,950-52,724,035 PXDNL
    nsv7061973inversion1nstd229human GRCh38 chr8: 51,413,883-51,417,573 , GRCh37.p13 chr8: 52,326,443-52,330,133 PXDNL
    nsv6857856copy number variation1nstd229human GRCh38 chr8: 51,773,055-51,773,425 , GRCh37.p13 chr8: 52,685,615-52,685,985 PXDNL, LOC105375833
    nsv6857614copy number variation1nstd229human GRCh38 chr8: 51,502,569-51,509,855 , GRCh37.p13 chr8: 52,415,129-52,422,415 PXDNL
    nsv6857206copy number variation1nstd229human GRCh38 chr8: 51,574,118-51,605,958 , GRCh37.p13 chr8: 52,486,678-52,518,518 PXDNL
    nsv6857174copy number variation1nstd229human GRCh38 chr8: 51,566,489-51,568,880 , GRCh37.p13 chr8: 52,479,049-52,481,440 PXDNL
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