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Items: 1 to 20 of 279

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5939434copy number variation1nstd209human GRCh38 chr16: 29,076,807-29,076,871 , GRCh37.p13 chr16: 29,088,128-29,088,192 RRN3P2
    nsv5930834copy number variation1nstd209human GRCh38 chr16: 29,086,937-29,087,070 , GRCh37.p13 chr16: 29,098,258-29,098,391 RRN3P2
    nsv5930508copy number variation1nstd209human GRCh38 chr16: 29,089,848-29,089,924 , GRCh37.p13 chr16: 29,101,169-29,101,245 RRN3P2
    nsv5663683insertion1nstd207human GRCh38 chr16: 29,089,861-29,089,861 , GRCh37.p13 chr16: 29,101,182-29,101,182 RRN3P2
    nsv5662114insertion1nstd207human GRCh38 chr16: 29,094,687-29,094,687 , GRCh37.p13 chr16: 29,106,008-29,106,008 RRN3P2
    nsv5660074insertion1nstd207human GRCh38 chr16: 29,107,930-29,107,930 , GRCh37.p13 chr16: 29,119,251-29,119,251 LOC101928215, RRN3P2
    nsv5647047insertion1nstd207human GRCh38 chr16: 29,074,913-29,074,913 , GRCh37.p13 chr16: 29,086,234-29,086,234 RRN3P2
    nsv5602793copy number variation1nstd207human GRCh38 chr16: 29,082,217-29,082,581 , GRCh37.p13 chr16: 29,093,538-29,093,902 RRN3P2
    nsv5595547copy number variation1nstd207human GRCh38 chr16: 29,076,807-29,076,871 , GRCh37.p13 chr16: 29,088,128-29,088,192 RRN3P2
    nsv5595273copy number variation1nstd207human GRCh38 chr16: 29,080,938-29,082,581 , GRCh37.p13 chr16: 29,092,259-29,093,902 RRN3P2
    nsv5588910copy number variation1nstd207human GRCh38 chr16: 29,080,938-29,081,216 , GRCh37.p13 chr16: 29,092,259-29,092,537 RRN3P2
    nsv5537806insertion1nstd206human GRCh38 chr16: 29,109,437-29,109,477 , GRCh37.p13 chr16: 29,120,758-29,120,798 RRN3P2, LOC101928215
    nsv5524578copy number variation1nstd206human GRCh38 chr16: 29,076,807-29,076,872 , GRCh37.p13 chr16: 29,088,128-29,088,193 RRN3P2
    nsv5514486copy number variation1nstd206human GRCh38 chr16: 29,086,953-29,087,055 , GRCh37.p13 chr16: 29,098,274-29,098,376 RRN3P2
    nsv5277176copy number variation1nstd204human GRCh38.p13 chr16: 29,092,703-29,096,681 , GRCh37.p13 chr16: 29,104,024-29,108,002 RRN3P2
    nsv5199839mobile element insertion1nstd203human GRCh38 chr16: 29,092,054-29,092,072 , GRCh37.p13 chr16: 29,103,375-29,103,393 RRN3P2
    nsv5152494mobile element insertion1nstd203human GRCh38 chr16: 29,072,853-29,072,869 , GRCh37.p13 chr16: 29,084,174-29,084,190 RRN3P2
    nsv5003414copy number variation1nstd200human GRCh38 chr16: 29,115,006-29,118,986 , GRCh37.p13 chr16: 29,126,327-29,130,307 RRN3P2
    nsv4856761copy number variation1nstd200human GRCh37 chr16: 29,126,327-29,130,307 , GRCh38.p12 chr16: 29,115,006-29,118,986 RRN3P2
    nsv4769395copy number variation1nstd102humanUncertain significance GRCh37 chr16: 28,483,631-29,332,591 , GRCh38.p12 chr16: 28,472,310-29,321,270 MIR4517, SULT1A1, 33 more genes
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