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Items: 1 to 20 of 183

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7058619inversion1nstd229human GRCh38 chr17: 49,389,100-51,159,770 , GRCh37.p13 chr17: 47,466,462-49,237,131 H1-9P, FLJ45513, 59 more genes
    nsv6986384copy number variation1nstd229human GRCh38 chr17: 49,089,556-55,863,152 , GRCh37.p13 chr17: 47,166,918-53,940,513 LOC107985002, FAM117A, 107 more genes
    nsv6985415copy number variation1nstd229human GRCh38 chr17: 50,743,521-50,877,038 , GRCh37.p13 chr17: 48,820,882-48,954,399 TOB1-AS1, RPL5P33, 5 more genes
    nsv6983143copy number variation1nstd229human GRCh38 chr17: 50,751,981-50,835,460 , GRCh37.p13 chr17: 48,829,342-48,912,821 MIR8059, LUC7L3, 2 more genes
    nsv6979726copy number variation1nstd229human GRCh38 chr17: 50,767,900-50,808,786 , GRCh37.p13 chr17: 48,845,261-48,886,147 MIR8059, ANKRD40CL
    nsv6586314inversion1nstd223human GRCh38 chr17: 50,760,052-50,761,312 , GRCh37.p13 chr17: 48,837,413-48,838,673 ANKRD40CL
    nsv6584617inversion1nstd223human GRCh38 chr17: 50,760,067-50,761,192 , GRCh37.p13 chr17: 48,837,428-48,838,553 ANKRD40CL
    nsv6532788copy number variation1nstd223human GRCh38 chr17: 50,757,885-50,759,415 , GRCh37.p13 chr17: 48,835,246-48,836,776 ANKRD40CL
    nsv6521119copy number variation1nstd223human GRCh38 chr17: 50,766,754-50,767,129 , GRCh37.p13 chr17: 48,844,115-48,844,490 MIR8059, ANKRD40CL
    nsv6517841copy number variation1nstd223human GRCh38 chr17: 50,767,900-50,808,786 , GRCh37.p13 chr17: 48,845,261-48,886,147 ANKRD40CL, MIR8059
    nsv5938611copy number variation1nstd209human GRCh38 chr17: 50,766,754-50,767,128 , GRCh37.p13 chr17: 48,844,115-48,844,489 ANKRD40CL, MIR8059
    nsv5594477copy number variation1nstd207human GRCh38 chr17: 50,766,754-50,767,128 , GRCh37.p13 chr17: 48,844,115-48,844,489 ANKRD40CL, MIR8059
    nsv5554090sequence alteration1nstd206human GRCh38 chr17: 32,109,732-67,925,723 , GRCh37.p13 chr17: 30,436,751-65,921,839 , APOH, 1099 more genes
    nsv5526966copy number variation1nstd206human GRCh38 chr17: 50,766,757-50,767,129 , GRCh37.p13 chr17: 48,844,118-48,844,490 ANKRD40CL, MIR8059
    nsv5393318copy number variation3nstd186human GRCh37 chr17: 48,844,118-48,844,490 , GRCh38.p12 chr17: 50,766,757-50,767,129 ANKRD40CL, MIR8059
    nsv5320922copy number variation1nstd204human GRCh37.p13 chr17: 48,844,115-48,844,492 , GRCh38.p13 chr17: 50,766,754-50,767,131 ANKRD40CL, MIR8059
    nsv5026393copy number variation1nstd200human GRCh38 chr17: 50,766,757-50,767,129 , GRCh37.p13 chr17: 48,844,118-48,844,490 MIR8059, ANKRD40CL
    nsv5026392copy number variation1nstd200human GRCh38 chr17: 50,762,791-50,762,874 , GRCh37.p13 chr17: 48,840,152-48,840,235 ANKRD40CL
    nsv5013811copy number variation1nstd200human GRCh38 chr17: 50,763,315-50,764,447 , GRCh37.p13 chr17: 48,840,676-48,841,808 ANKRD40CL
    nsv5013810copy number variation1nstd200human GRCh38 chr17: 50,757,792-50,759,468 , GRCh37.p13 chr17: 48,835,153-48,836,829 ANKRD40CL
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