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Items: 1 to 20 of 160

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5563034sequence alteration1nstd206human GRCh38 chr17: 47,820,538-47,820,543 , GRCh37.p13 chr17: 45,897,904-45,897,909 OSBPL7
    nsv5554090sequence alteration1nstd206human GRCh38 chr17: 32,109,732-67,925,723 , GRCh37.p13 chr17: 30,436,751-65,921,839 , APOH, 1099 more genes
    nsv5514273copy number variation1nstd206human GRCh38 chr17: 47,820,523-47,821,423 , GRCh37.p13 chr17: 45,897,889-45,898,789 OSBPL7, MRPL10
    nsv5358909translocation1nstd200human GRCh38 chr17: 47,820,237-47,820,237 , GRCh38 chr17: 47,820,135-47,820,135 , GRCh37.p13 chr17: 45,897,603-45,897,603 , GRCh37.p13 chr17: 45,897,501-45,897,501 OSBPL7
    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
    nsv5013773copy number variation1nstd200human GRCh38 chr17: 47,820,543-47,821,403 , GRCh37.p13 chr17: 45,897,909-45,898,769 MRPL10, OSBPL7
    nsv4624248copy number variation1nstd183human GRCh37 chr17: 45,888,220-45,888,871 , GRCh38.p12 chr17: 47,810,854-47,811,505 OSBPL7
    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
    nsv4265404copy number variation1nstd166human GRCh37.p13 chr17: 45,889,746-45,908,919 , GRCh38.p12 chr17: 47,812,380-47,831,553 OSBPL7, LRRC46, 1 more genes
    nsv4264113copy number variation1nstd166human GRCh37.p13 chr17: 45,897,904-45,898,169 , GRCh38.p12 chr17: 47,820,538-47,820,803 OSBPL7
    nsv4255808copy number variation1nstd166human GRCh37.p13 chr17: 45,897,902-45,898,769 , GRCh38.p12 chr17: 47,820,536-47,821,403 OSBPL7, MRPL10
    nsv3966201copy number variation1nstd168human GRCh38 chr17: 47,775,195-47,811,038 , GRCh37.p13 chr17: 45,852,561-45,888,404 OSBPL7
    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
    nsv3914783copy number variation1nstd102humanPathogenic NCBI36 chr17: 16,698,288-78,654,742 , GRCh37.p13 chr17: 16,757,563-81,048,189 , GRCh38.p12 chr17: 16,854,249-83,103,577 LOC105371922, GJD3, 1855 more genes
    nsv3913552copy number variation1nstd102humanPathogenic GRCh38 chr17: 36,449,220-75,053,130 , NCBI36 chr17: 54,950,518-70,560,820 , GRCh37 chr17: 57,595,736-73,049,225 RNU6-131P, ZNF652, 1075 more genes
    nsv3911811copy number variation1nstd102humanPathogenic NCBI36 chr17: 31,824,931-78,654,742 , GRCh37.p13 chr17: 34,750,818-81,048,189 , GRCh38.p12 chr17: 36,382,248-83,103,577 PRPSAP1, CACNG1, 1350 more genes
    nsv3911563copy number variation1nstd102humanPathogenic NCBI36 chr17: 45,918,236-63,677,950 , GRCh37 chr17: 48,563,237-65,936,105 , GRCh38 chr17: 36,449,220-68,170,214 PLEKHH3, CHCT1, 958 more genes
    nsv3909511copy number variation1nstd102humanPathogenic GRCh37 chr17: 42,580,684-81,085,615 , GRCh38.p12 chr17: 44,503,316-83,137,846 FOXK2, SOCS3-DT, 958 more genes
    nsv3907261copy number variation2nstd102humanPathogenic GRCh37 chr17: 526-81,041,938 , GRCh38.p12 chr17: 150,733-83,084,062 SMURF2, LOC112268199, 2366 more genes
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