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Items: 1 to 20 of 723

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5903839copy number variation1nstd209human GRCh38 chr5: 79,180,365-84,539,350 , GRCh37.p13 chr5: 78,476,188-83,835,168 , ANKRD34B, 84 more genes
    nsv5900933copy number variation1nstd209human GRCh38 chr5: 82,139,547-82,139,663 , GRCh37.p13 chr5: 81,435,366-81,435,482 ATG10
    nsv5900803copy number variation1nstd209human GRCh38 chr5: 81,981,415-81,987,555 , GRCh37.p13 chr5: 81,277,234-81,283,374 ATG10
    nsv5898409copy number variation1nstd209human GRCh38 chr5: 82,170,150-82,170,257 , GRCh37.p13 chr5: 81,465,969-81,466,076 ATG10
    nsv5843506copy number variation2nstd209human GRCh38 chr5: 82,126,865-82,134,810 , GRCh37.p13 chr5: 81,422,684-81,430,629 ATG10
    nsv5718218mobile element insertion1nstd211human GRCh38 chr5: 82,008,452-82,008,452 , GRCh37.p13 chr5: 81,304,271-81,304,271 PPIAP11, ATG10
    nsv5715624mobile element insertion1nstd211human GRCh38 chr5: 82,174,796-82,174,796 , GRCh37.p13 chr5: 81,470,615-81,470,615 ATG10
    nsv5692788mobile element insertion2nstd211human GRCh38 chr5: 82,015,145-82,015,145 , GRCh37.p13 chr5: 81,310,964-81,310,964 ATG10
    nsv5690142mobile element insertion1nstd211human GRCh38 chr5: 82,007,943-82,007,943 , GRCh37.p13 chr5: 81,303,762-81,303,762 PPIAP11, ATG10
    nsv5689293mobile element insertion1nstd211human GRCh38 chr5: 82,084,687-82,084,687 , GRCh37.p13 chr5: 81,380,506-81,380,506 ATG10
    nsv5683372mobile element insertion1nstd211human GRCh38 chr5: 82,059,973-82,059,973 , GRCh37.p13 chr5: 81,355,792-81,355,792 ATG10
    nsv5682508mobile element insertion2nstd211human GRCh38 chr5: 82,145,063-82,145,063 , GRCh37.p13 chr5: 81,440,882-81,440,882 ATG10
    nsv5674423mobile element insertion1nstd211human GRCh38 chr5: 82,010,592-82,010,592 , GRCh37.p13 chr5: 81,306,411-81,306,411 ATG10, PPIAP11
    nsv5643196insertion1nstd207human GRCh38 chr5: 82,140,209-82,140,209 , GRCh37.p13 chr5: 81,436,028-81,436,028 ATG10
    nsv5639199insertion1nstd207human GRCh38 chr5: 81,993,360-81,993,360 , GRCh37.p13 chr5: 81,289,179-81,289,179 ATG10
    nsv5632968insertion1nstd207human GRCh38 chr5: 82,140,339-82,140,339 , GRCh37.p13 chr5: 81,436,158-81,436,158 ATG10
    nsv5631879insertion1nstd207human GRCh38 chr5: 82,140,192-82,140,192 , GRCh37.p13 chr5: 81,436,011-81,436,011 ATG10
    nsv5631459insertion2nstd207human GRCh38 chr5: 81,993,359-81,993,359 , GRCh37.p13 chr5: 81,289,178-81,289,178 ATG10
    nsv5626062insertion1nstd207human GRCh38 chr5: 82,140,420-82,140,420 , GRCh37.p13 chr5: 81,436,239-81,436,239 ATG10
    nsv5580316copy number variation1nstd207human GRCh38 chr5: 81,983,417-81,983,466 , GRCh37.p13 chr5: 81,279,236-81,279,285 ATG10
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