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Items: 1 to 20 of 230

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7077952inversion1nstd229human GRCh38 chr17: 66,832,726-66,834,968 , GRCh37.p13 chr17: 64,828,844-64,831,086 CACNG5
    nsv7077537inversion1nstd229human GRCh38 chr17: 64,968,697-68,255,761 , GRCh37.p13 chr17: 62,964,815-65,936,105 SNORA38B, PRKCA-AS1, 52 more genes
    nsv7070779inversion1nstd229human GRCh38 chr17: 64,711,213-68,088,947 , GRCh37.p13 chr17: 62,707,331-65,936,105 MICOS10P2, LOC100420638, 61 more genes
    nsv7070446inversion1nstd229human GRCh38 chr17: 65,003,854-68,220,374 , GRCh37.p13 chr17: 62,999,972-65,936,105 SH3GL1P3, AXIN2, 51 more genes
    nsv7059173inversion1nstd229human GRCh38 chr17: 65,003,895-68,220,334 , GRCh37.p13 chr17: 63,000,013-65,936,105 RPSAP67, HELZ-AS1, 51 more genes
    nsv6997151copy number variation1nstd229human GRCh38 chr17: 66,746,420-66,851,037 , GRCh37.p13 chr17: 64,742,538-64,847,155 PRKCA, CACNG5, 1 more genes
    nsv6997065copy number variation1nstd229human GRCh38 chr17: 66,841,178-66,844,719 , GRCh37.p13 chr17: 64,837,296-64,840,837 CACNG5
    nsv6992203copy number variation1nstd229human GRCh38 chr17: 66,828,322-66,837,018 , GRCh37.p13 chr17: 64,824,440-64,833,136 CACNG5
    nsv6990619copy number variation1nstd229human GRCh38 chr17: 66,892,601-66,905,500 , GRCh37.p13 chr17: 64,888,718-64,901,617 CACNG5, RNA5SP446
    nsv6990323copy number variation1nstd229human GRCh38 chr17: 66,860,351-66,862,734 , GRCh37.p13 chr17: 64,856,469-64,858,852 CACNG5
    nsv6990275copy number variation1nstd229human GRCh38 chr17: 66,887,601-66,895,700 , GRCh37.p13 chr17: 64,883,718-64,891,817 CACNG5, RNA5SP446
    nsv6990264copy number variation1nstd229human GRCh38 chr17: 66,895,228-66,896,031 , GRCh37.p13 chr17: 64,891,345-64,892,148 CACNG5, RNA5SP446
    nsv6987397copy number variation1nstd229human GRCh38 chr17: 66,090,324-66,928,705 , GRCh37.p13 chr17: 64,086,442-64,924,822 PSMD7P1, PRKCA-AS1, 10 more genes
    nsv6986325copy number variation1nstd229human GRCh38 chr17: 66,887,501-66,895,800 , GRCh37.p13 chr17: 64,883,618-64,891,917 RNA5SP446, CACNG5
    nsv6984887copy number variation1nstd229human GRCh38 chr17: 66,867,110-66,871,343 , GRCh37.p13 chr17: 64,863,228-64,867,461 CACNG5
    nsv6979532copy number variation1nstd229human GRCh38 chr17: 66,893,280-66,905,489 , GRCh37.p13 chr17: 64,889,397-64,901,606 RNA5SP446, CACNG5
    nsv6534681copy number variation1nstd223human GRCh38 chr17: 66,886,677-66,887,217 , GRCh37.p13 chr17: 64,882,794-64,883,334 CACNG5
    nsv6519451copy number variation1nstd223human GRCh38 chr17: 66,887,559-66,895,773 , GRCh37.p13 chr17: 64,883,676-64,891,890 RNA5SP446, CACNG5
    nsv6250956mobile element insertion1nstd215human GRCh38 chr17: 66,865,268-66,865,268 , GRCh37.p13 chr17: 64,861,386-64,861,386 CACNG5
    nsv6133070copy number variation1nstd213human GRCh37 chr17: 62,460,000-73,800,001 , GRCh38.p12 chr17: 64,464,645-75,803,920 APOH, CACNG1, 225 more genes
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