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Items: 1 to 20 of 261

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148088copy number variation1nstd102humanUncertain significance GRCh37 chr17: 25,263,507-27,829,791 , GRCh38.p12 chr17: 26,936,481-29,502,773 RNU4-34P, RNU6-711P, 95 more genes
    nsv7095086copy number variation1nstd102humanPathogenic GRCh37 chr17: 27,573,882-29,576,157 , GRCh38.p12 chr17: 29,246,864-31,249,139 LOC107984990, ADAP2, 59 more genes
    nsv7095084copy number variation1nstd102humanUncertain significance GRCh37 chr17: 26,684,694-29,701,173 , GRCh38.p12 chr17: 28,357,671-31,374,155 RNU6-1267P, PIPOX, 114 more genes
    nsv7094962copy number variation1nstd102humanUncertain significance GRCh37 chr17: 26,684,694-27,581,367 , GRCh38.p12 chr17: 28,357,671-29,254,349 FLOT2, SPAG5-AS1, 50 more genes
    nsv7077065inversion1nstd229human GRCh38 chr17: 29,289,926-29,290,648 , GRCh37.p13 chr17: 27,616,944-27,617,666 NUFIP2
    nsv7076709inversion1nstd229human GRCh38 chr17: 29,265,017-29,274,901 , GRCh37.p13 chr17: 27,592,035-27,601,919 NUFIP2
    nsv7062182inversion1nstd229human GRCh38 chr17: 27,487,612-31,414,648 , GRCh37.p13 chr17: 25,814,638-29,741,666 ERAL1, SARM1, 140 more genes
    nsv6994190copy number variation1nstd229human GRCh38 chr17: 29,266,195-29,267,134 , GRCh37.p13 chr17: 27,593,213-27,594,152 NUFIP2
    nsv6992226copy number variation1nstd229human GRCh38 chr17: 29,254,918-29,255,075 , GRCh37.p13 chr17: 27,581,936-27,582,093 NUFIP2, CRYBA1
    nsv6985266copy number variation1nstd229human GRCh38 chr17: 29,224,242-29,254,148 , GRCh37.p13 chr17: 27,551,260-27,581,166 CRYBA1, NUFIP2
    nsv6983682copy number variation1nstd229human GRCh38 chr17: 29,253,488-29,253,850 , GRCh37.p13 chr17: 27,580,506-27,580,868 NUFIP2, CRYBA1
    nsv6982932copy number variation1nstd229human GRCh38 chr17: 29,271,156-29,273,842 , GRCh37.p13 chr17: 27,598,174-27,600,860 NUFIP2
    nsv6980488copy number variation1nstd229human GRCh38 chr17: 29,280,887-29,280,917 , GRCh37.p13 chr17: 27,607,905-27,607,935 NUFIP2
    nsv6980471copy number variation1nstd229human GRCh38 chr17: 29,274,301-29,277,400 , GRCh37.p13 chr17: 27,601,319-27,604,418 NUFIP2
    nsv6980451copy number variation1nstd229human GRCh38 chr17: 29,103,792-32,176,512 , GRCh37.p13 chr17: 27,430,810-30,503,531 SMURF2P1-LRRC37BP1, RNU6-990P, 90 more genes
    nsv6980156copy number variation1nstd229human GRCh38 chr17: 29,272,001-29,283,500 , GRCh37.p13 chr17: 27,599,019-27,610,518 NUFIP2
    nsv6637662copy number variation1nstd102humanUncertain significance GRCh37 chr17: 27,552,278-27,842,559 , GRCh38.p12 chr17: 29,225,260-29,515,541 RNU6-1034P, RPL35AP35, 6 more genes
    nsv6584490inversion1nstd223human GRCh38 chr17: 29,279,660-29,280,742 , GRCh37.p13 chr17: 27,606,678-27,607,760 NUFIP2
    nsv6513573copy number variation1nstd223human GRCh38 chr17: 29,271,997-29,283,539 , GRCh37.p13 chr17: 27,599,015-27,610,557 NUFIP2
    nsv6508214copy number variation1nstd223human GRCh38 chr17: 29,284,428-29,285,025 , GRCh37.p13 chr17: 27,611,446-27,612,043 NUFIP2
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