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Items: 1 to 20 of 203

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5694270mobile element insertion2nstd211human GRCh38 chr7: 94,620,264-94,620,264 , GRCh37.p13 chr7: 94,249,576-94,249,576 CASD1, SGCE
    nsv5691341mobile element insertion1nstd211human GRCh38 chr7: 94,645,879-94,645,879 , GRCh37.p13 chr7: 94,275,191-94,275,191 SGCE
    nsv5690462mobile element insertion1nstd211human GRCh38 chr7: 94,617,099-94,617,099 , GRCh37.p13 chr7: 94,246,411-94,246,411 CASD1, SGCE
    nsv5673939copy number variation1nstd102humanPathogenic GRCh37 chr7: 94,252,627-94,252,719 , GRCh38.p12 chr7: 94,623,315-94,623,407 CASD1, SGCE
    nsv5673938copy number variation1nstd102humanPathogenic GRCh37 chr7: 94,228,081-94,232,770 , GRCh38.p12 chr7: 94,598,769-94,603,458 CASD1, SGCE
    nsv5556846sequence alteration1nstd206human GRCh38 chr7: 2,511,247-157,318,976 , GRCh37.p13 chr7: 2,550,881-157,111,670 , AHR, 2675 more genes
    nsv5488057copy number variation1nstd206human GRCh38 chr7: 94,644,910-94,645,195 , GRCh37.p13 chr7: 94,274,222-94,274,507 SGCE
    nsv5395254mobile element insertion1nstd206human GRCh38 chr7: 94,620,264-94,620,315 , GRCh37.p13 chr7: 94,249,576-94,249,627 CASD1, SGCE
    nsv5394794mobile element insertion1nstd206human GRCh38 chr7: 94,617,099-94,617,150 , GRCh37.p13 chr7: 94,246,411-94,246,462 SGCE, CASD1
    nsv5381780copy number variation1nstd102humanPathogenic GRCh37 chr7: 87,477,185-100,333,327 , GRCh38.p12 chr7: 87,847,870-100,735,704 ARPC1A, LOC112267858, 265 more genes
    nsv5381552copy number variation1nstd102humanUncertain significance GRCh37 chr7: 94,285,282-94,285,430 , GRCh38.p12 chr7: 94,655,970-94,656,118 SGCE, PEG10
    nsv5321926inversion1nstd204human GRCh37.p13 chr7: 93,899,155-99,360,080 , GRCh38.p13 chr7: 94,269,843-99,762,457 , CYP3A51P, 118 more genes
    nsv5104178mobile element insertion1nstd203human GRCh38 chr7: 94,620,248-94,620,264 , GRCh37.p13 chr7: 94,249,560-94,249,576 CASD1, SGCE
    nsv5103965mobile element insertion1nstd203human GRCh38 chr7: 94,617,084-94,617,099 , GRCh37.p13 chr7: 94,246,396-94,246,411 SGCE, CASD1
    nsv5102170mobile element insertion1nstd203human GRCh38 chr7: 94,586,061-94,586,087 , GRCh37.p13 chr7: 94,215,373-94,215,399 SGCE, CASD1
    nsv5039775inversion1nstd200human GRCh38 chr7: 22,938,090-134,148,361 , GRCh37.p13 chr7: 22,977,709-133,833,114 , NFE4, 1832 more genes
    nsv5029742inversion1nstd200human GRCh38 chr7: 79,688,546-147,673,588 , GRCh37.p13 chr7: 79,317,862-147,370,680 , LOC100533722, 1168 more genes
    nsv4964973copy number variation1nstd200human GRCh38 chr7: 94,644,910-94,645,195 , GRCh37.p13 chr7: 94,274,222-94,274,507 SGCE
    nsv4957720copy number variation1nstd200human GRCh38 chr7: 94,646,691-94,647,631 , GRCh37.p13 chr7: 94,276,003-94,276,943 SGCE
    nsv4957719copy number variation1nstd200human GRCh38 chr7: 94,589,992-94,590,147 , GRCh37.p13 chr7: 94,219,304-94,219,459 CASD1, SGCE
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