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Items: 1 to 20 of 180

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5707072mobile element insertion1nstd211human GRCh38 chr17: 47,874,541-47,874,541 , GRCh37.p13 chr17: 45,951,907-45,951,907 SP6
    nsv5702681mobile element insertion1nstd211human GRCh38 chr17: 47,873,148-47,873,148 , GRCh37.p13 chr17: 45,950,514-45,950,514 SP6
    nsv5554090sequence alteration1nstd206human GRCh38 chr17: 32,109,732-67,925,723 , GRCh37.p13 chr17: 30,436,751-65,921,839 , APOH, 1099 more genes
    nsv5431332mobile element insertion1nstd206human GRCh38 chr17: 47,874,541-47,874,592 , GRCh37.p13 chr17: 45,951,907-45,951,958 SP6
    nsv5413991mobile element insertion1nstd206human GRCh38 chr17: 47,873,148-47,873,199 , GRCh37.p13 chr17: 45,950,514-45,950,565 SP6
    nsv5288564copy number variation1nstd204human GRCh38.p13 chr17: 47,781,201-48,222,600 , GRCh37.p13 chr17: 45,858,567-46,299,962 CDK5RAP3, NFE2L1, 20 more genes
    nsv5159060mobile element insertion1nstd203human GRCh38 chr17: 47,874,526-47,874,539 , GRCh37.p13 chr17: 45,951,892-45,951,905 SP6
    nsv5140508mobile element insertion1nstd203human GRCh38 chr17: 47,873,130-47,873,148 , GRCh37.p13 chr17: 45,950,496-45,950,514 SP6
    nsv5026291copy number variation1nstd200human GRCh38 chr17: 47,855,802-47,863,923 , GRCh37.p13 chr17: 45,933,168-45,941,289 SP6
    nsv5026290copy number variation1nstd200human GRCh38 chr17: 47,843,823-47,846,111 , GRCh37.p13 chr17: 45,921,189-45,923,477 SP6
    nsv4867188copy number variation1nstd200human GRCh37 chr17: 45,921,189-45,923,477 , GRCh38.p12 chr17: 47,843,823-47,846,111 SP6
    nsv4769514mobile element deletion1nstd200human GRCh37 chr17: 45,954,158-45,954,460 , GRCh38.p12 chr17: 47,876,792-47,877,094 SP6
    nsv4513485mobile element insertion1nstd166human GRCh37.p13 chr17: 45,951,892-45,951,892 , GRCh38.p12 chr17: 47,874,526-47,874,526 SP6
    nsv4501684mobile element insertion1nstd166human GRCh37.p13 chr17: 45,950,496-45,950,496 , GRCh38.p12 chr17: 47,873,130-47,873,130 SP6
    nsv4436018complex substitution1nstd102humanUncertain significance GRCh37 chr17: 45,008,570-45,994,044 , GRCh38.p12 chr17: 46,931,204-47,916,678 CDC27, ITGB3, 30 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
    nsv4271854copy number variation1nstd166human GRCh37.p13 chr17: 45,913,073-46,111,423 , GRCh38.p12 chr17: 47,835,707-48,034,057 SP2-AS1, LRRC46, 9 more genes
    nsv4257979copy number variation1nstd166human GRCh37.p13 chr17: 45,941,144-45,941,693 , GRCh38.p12 chr17: 47,863,778-47,864,327 SP6
    nsv4255417copy number variation1nstd166human GRCh37.p13 chr17: 45,952,857-45,952,919 , GRCh38.p12 chr17: 47,875,491-47,875,553 SP6
    nsv3919205copy number variation1nstd102humanUncertain significance NCBI36 chr17: 43,118,852-43,419,326 , GRCh37 chr17: 45,763,853-46,064,327 , GRCh38 chr17: 47,686,487-47,986,961 TBKBP1, OSBPL7, 11 more genes
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