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Items: 1 to 20 of 886

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7050019inversion1nstd229human GRCh38 chr3: 195,136,005-195,209,352 , GRCh37.p13 chr3: 194,856,734-194,930,081 RN7SL36P, XXYLT1-AS2, 2 more genes
    nsv7043719inversion1nstd229human GRCh38 chr3: 194,788,231-195,129,703 , GRCh37.p13 chr3: 194,508,960-194,850,432 XXYLT1-AS1, LOC107986173, 4 more genes
    nsv7040982inversion1nstd229human GRCh38 chr3: 193,802,086-196,241,826 , GRCh37.p13 chr3: 193,519,875-195,968,697 CPN2, RNU6ATAC24P, 73 more genes
    nsv6737514copy number variation1nstd229human GRCh38 chr3: 195,210,045-195,257,056 , GRCh37.p13 chr3: 194,930,774-194,977,785 RNU6-25P, XXYLT1
    nsv6736381copy number variation1nstd229human GRCh38 chr3: 195,143,847-195,144,287 , GRCh37.p13 chr3: 194,864,576-194,865,016 XXYLT1
    nsv6735703copy number variation1nstd229human GRCh38 chr3: 194,749,386-195,131,549 , GRCh37.p13 chr3: 194,470,115-194,852,278 FAM151AP1, XXYLT1-AS1, 7 more genes
    nsv6735504copy number variation1nstd229human GRCh38 chr3: 195,209,961-195,210,021 , GRCh37.p13 chr3: 194,930,690-194,930,750 XXYLT1
    nsv6734934copy number variation1nstd229human GRCh38 chr3: 195,259,716-195,259,740 , GRCh37.p13 chr3: 194,980,445-194,980,469 XXYLT1
    nsv6734834copy number variation1nstd229human GRCh38 chr3: 195,074,611-195,086,623 , GRCh37.p13 chr3: 194,795,340-194,807,352 XXYLT1
    nsv6731714copy number variation1nstd229human GRCh38 chr3: 192,378,501-195,488,100 , GRCh37.p13 chr3: 192,096,290-195,214,903 LSG1, MB21D2, 61 more genes
    nsv6731462copy number variation1nstd229human GRCh38 chr3: 195,176,576-195,187,880 , GRCh37.p13 chr3: 194,897,305-194,908,609 XXYLT1
    nsv6731145copy number variation1nstd229human GRCh38 chr3: 195,100,469-195,100,540 , GRCh37.p13 chr3: 194,821,198-194,821,269 XXYLT1
    nsv6729289copy number variation1nstd229human GRCh38 chr3: 195,201,399-195,330,006 , GRCh37.p13 chr3: 194,922,128-195,050,735 RNU6-25P, XXYLT1, 1 more genes
    nsv6729043copy number variation1nstd229human GRCh38 chr3: 195,099,278-195,115,234 , GRCh37.p13 chr3: 194,820,007-194,835,963 XXYLT1
    nsv6728604copy number variation1nstd229human GRCh38 chr3: 195,182,800-195,330,490 , GRCh37.p13 chr3: 194,903,529-195,051,219 ACAP2, XXYLT1, 1 more genes
    nsv6728170copy number variation1nstd229human GRCh38 chr3: 195,206,251-195,210,038 , GRCh37.p13 chr3: 194,926,980-194,930,767 XXYLT1
    nsv6727504copy number variation1nstd229human GRCh38 chr3: 195,263,421-195,263,801 , GRCh37.p13 chr3: 194,984,150-194,984,530 XXYLT1
    nsv6726845copy number variation1nstd229human GRCh38 chr3: 195,166,700-195,177,845 , GRCh37.p13 chr3: 194,887,429-194,898,574 XXYLT1
    nsv6726657copy number variation1nstd229human GRCh38 chr3: 195,065,654-195,066,739 , GRCh37.p13 chr3: 194,786,383-194,787,468 XXYLT1
    nsv6726441copy number variation1nstd229human GRCh38 chr3: 195,198,805-195,201,436 , GRCh37.p13 chr3: 194,919,534-194,922,165 XXYLT1
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