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Items: 1 to 20 of 307

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5974799inversion1nstd209human GRCh38 chr19: 12,342,936-19,691,231 , GRCh37.p13 chr19: 12,453,750-19,802,040 , GET3, 322 more genes
    nsv5968278insertion1nstd209human GRCh38 chr19: 14,090,084-14,090,084 , GRCh37.p13 chr19: 14,200,896-14,200,896 SAMD1, PRKACA
    nsv5944649copy number variation1nstd209human GRCh38 chr19: 14,112,410-14,112,464 , GRCh37.p13 chr19: 14,223,222-14,223,276 PRKACA
    nsv5705531mobile element insertion1nstd211human GRCh38 chr19: 14,090,575-14,090,575 , GRCh37.p13 chr19: 14,201,387-14,201,387 PRKACA, SAMD1
    nsv5659559insertion1nstd207human GRCh38 chr19: 14,108,729-14,108,729 , GRCh37.p13 chr19: 14,219,541-14,219,541 PRKACA
    nsv5645219insertion1nstd207human GRCh38 chr19: 14,090,084-14,090,084 , GRCh37.p13 chr19: 14,200,896-14,200,896 PRKACA, SAMD1
    nsv5533514copy number variation1nstd206human GRCh38 chr19: 14,091,271-14,091,399 , GRCh37.p13 chr19: 14,202,083-14,202,211 PRKACA
    nsv5532980copy number variation1nstd206human GRCh38 chr19: 14,089,364-14,089,784 , GRCh37.p13 chr19: 14,200,176-14,200,596 SAMD1, PRKACA
    nsv5528029copy number variation1nstd206human GRCh38 chr19: 14,112,411-14,112,465 , GRCh37.p13 chr19: 14,223,223-14,223,277 PRKACA
    nsv5522157copy number variation1nstd206human GRCh38 chr19: 14,118,253-14,118,323 , GRCh37.p13 chr19: 14,229,065-14,229,135 ASF1B, PRKACA
    nsv5300223copy number variation1nstd204human GRCh38.p13 chr19: 13,638,301-14,767,500 , GRCh37.p13 chr19: 13,749,115-14,878,312 , SNORA104, 53 more genes
    nsv5295552copy number variation1nstd204human GRCh38.p13 chr19: 13,937,101-14,461,200 , GRCh37.p13 chr19: 14,047,914-14,572,012 , ASF1B, 20 more genes
    nsv5293679copy number variation1nstd204human GRCh38.p13 chr19: 14,093,901-14,096,100 , GRCh37.p13 chr19: 14,204,713-14,206,912 PRKACA
    nsv5172642mobile element insertion1nstd203human GRCh38 chr19: 14,108,729-14,108,745 , GRCh37.p13 chr19: 14,219,541-14,219,557 PRKACA
    nsv5170689mobile element insertion1nstd203human GRCh38 chr19: 14,109,985-14,109,985 , GRCh37.p13 chr19: 14,220,797-14,220,797 PRKACA
    nsv5163130mobile element insertion1nstd203human GRCh38 chr19: 14,095,679-14,095,689 , GRCh37.p13 chr19: 14,206,491-14,206,501 PRKACA
    nsv5041043inversion1nstd200human GRCh38 chr19: 11,963,569-20,150,886 , GRCh37.p13 chr19: 12,074,384-20,193,556 , USE1, 369 more genes
    nsv5011923copy number variation1nstd200human GRCh38 chr19: 14,104,136-14,105,240 , GRCh37.p13 chr19: 14,214,948-14,216,052 PRKACA
    nsv4673781copy number variation2nstd186human GRCh37 chr19: 14,201,114-14,201,241 , GRCh38.p12 chr19: 14,090,302-14,090,429 PRKACA, SAMD1
    nsv4673449copy number variation1nstd186human GRCh37 chr19: 14,201,117-14,201,161 , GRCh38.p12 chr19: 14,090,305-14,090,349 PRKACA, SAMD1
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