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Items: 1 to 20 of 182

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5554090sequence alteration1nstd206human GRCh38 chr17: 32,109,732-67,925,723 , GRCh37.p13 chr17: 30,436,751-65,921,839 , APOH, 1099 more genes
    nsv5013724copy number variation1nstd200human GRCh38 chr17: 43,313,216-43,589,560 , GRCh37.p13 chr17: 41,390,570-41,666,928 RNU6-971P, ARL4D, 11 more genes
    nsv4864660copy number variation1nstd200human GRCh37 chr17: 41,390,570-41,666,928 , GRCh38.p12 chr17: 43,313,216-43,589,560 ARL4D, DHX8, 11 more genes
    nsv4729870copy number variation1nstd102humanUncertain significance GRCh37 chr17: 41,221,565-41,775,043 , GRCh38.p12 chr17: 43,069,548-43,697,675 LOC105371785, RNU6-406P, 24 more genes
    nsv4680708copy number variation1nstd189human GRCh37.p13 chr17: 41,357,686-42,167,307 , GRCh38.p12 chr17: 43,205,667-44,089,939 , ARL4D, 41 more genes
    nsv4675549copy number variation1nstd102humanUncertain significance GRCh37 chr17: 41,399,892-41,736,186 , GRCh38.p12 chr17: 43,322,528-43,658,818 DHX8, RNU6-1137P, 12 more genes
    nsv4675311copy number variation1nstd102humanUncertain significance GRCh37 chr17: 41,384,515-41,599,383 , GRCh38.p12 chr17: 43,307,153-43,522,015 ARL4D, RNU6-971P, 10 more genes
    nsv4674980copy number variation1nstd102humanUncertain significance GRCh37 chr17: 41,399,892-42,125,780 , GRCh38.p12 chr17: 43,322,528-44,048,412 RPL29P31, MEOX1, 34 more genes
    nsv4625110copy number variation1nstd183human GRCh37 chr17: 41,415,522-41,613,607 , GRCh38.p12 chr17: 43,338,154-43,536,239 RNU6-406P, LINC00910, 11 more genes
    nsv4457708copy number variation1nstd102humanUncertain significance GRCh37 chr17: 41,440,122-41,745,139 , GRCh38.p12 chr17: 43,362,754-43,667,771 RNU2-4P, RNU6-470P, 13 more genes
    nsv4421838copy number variation1nstd174human GRCh37 chr17: 41,399,657-41,869,317 , GRCh38.p12 chr17: 43,322,294-43,791,949 LINC00910, LINC02594, 18 more genes
    nsv4368311copy number variation1nstd173human GRCh37 chr17: 41,384,516-42,395,351 , GRCh38.p12 chr17: 43,307,154-44,317,983 , LOC105371789, 55 more genes
    nsv4330632inversion1nstd166human GRCh37.p13 chr17: 18,838,526-72,042,289 , GRCh38.p12 chr17: 18,935,213-74,046,150 , ACACA, 1499 more genes
    nsv4267582copy number variation1nstd166human GRCh37.p13 chr17: 41,443,000-41,687,000 , GRCh38.p12 chr17: 43,365,632-43,609,632 LINC00910, RNU6-470P, 11 more genes
    nsv3968801insertion1nstd168human GRCh37.p13 chr17: 41,368,996-41,509,271 , GRCh38 chr17: 43,216,977-43,431,903 ARL4D, RNU2-1, 7 more genes
    nsv3967439copy number variation1nstd168human GRCh38 chr17: 43,211,742-43,419,113 , GRCh37.p13 chr17: 41,363,761-41,496,481 RNU2-4P, LOC105371785, 8 more genes
    nsv3967091inversion1nstd168human GRCh37.p13 chr17: 41,478,949-41,496,481 , GRCh38 chr17: 43,401,581-43,419,113 ARL4D, RNU6-470P
    nsv3923117copy number variation1nstd102humanUncertain significance GRCh38 chr17: 43,080,123-43,897,875 , NCBI36 chr17: 38,485,666-39,330,769 , GRCh37 chr17: 41,232,140-41,975,243 RNU6-470P, CCDC200, 33 more genes
    nsv3922353copy number variation1nstd102humanUncertain significance GRCh38 chr17: 43,088,882-43,865,172 , GRCh37 chr17: 41,240,899-41,942,540 , NCBI36 chr17: 38,494,425-39,298,066 NBR1, LOC107985077, 31 more genes
    nsv3921716copy number variation1nstd102humanUncertain significance NCBI36 chr17: 38,456,488-39,330,777 , GRCh38 chr17: 43,050,945-43,897,883 , GRCh37 chr17: 41,202,962-41,975,251 LINC02594, MEOX1, 33 more genes
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