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Items: 1 to 20 of 287

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7071647inversion1nstd229human GRCh38 chr15: 54,705,615-56,525,786 , GRCh37.p13 chr15: 54,997,813-56,817,984 RN7SL568P, CD24P2, 21 more genes
    nsv7070136inversion1nstd229human GRCh38 chr15: 55,506,327-55,625,589 , GRCh37.p13 chr15: 55,798,525-55,917,787 DNAAF4, PRTG, 1 more genes
    nsv7069841inversion1nstd229human GRCh38 chr15: 55,108,583-62,405,114 , GRCh37.p13 chr15: 55,400,781-62,697,313 LOC105370834, RPL21P14, 118 more genes
    nsv7063318inversion1nstd229human GRCh38 chr15: 55,544,043-55,556,358 , GRCh37.p13 chr15: 55,836,241-55,848,556 PYGO1
    nsv7063220inversion1nstd229human GRCh38 chr15: 55,051,178-56,314,633 , GRCh37.p13 chr15: 55,343,376-56,606,831 CCPG1, PIGBOS1, 19 more genes
    nsv7059635inversion1nstd229human GRCh38 chr15: 51,716,761-55,548,818 , GRCh37.p13 chr15: 52,008,958-55,841,016 CCPG1, LOC105370823, 51 more genes
    nsv7059534inversion1nstd229human GRCh38 chr15: 51,726,660-55,605,328 , GRCh37.p13 chr15: 52,018,857-55,897,526 HNRNPA1P74, MYO5C, 50 more genes
    nsv6976599copy number variation1nstd229human GRCh38 chr15: 55,571,662-55,664,750 , GRCh37.p13 chr15: 55,863,860-55,956,948 PYGO1, PRTG
    nsv6975117copy number variation1nstd229human GRCh38 chr15: 55,269,699-55,652,454 , GRCh37.p13 chr15: 55,561,897-55,944,652 PIGB, RAB27A, 9 more genes
    nsv6973173copy number variation1nstd229human GRCh38 chr15: 55,553,553-55,556,612 , GRCh37.p13 chr15: 55,845,751-55,848,810 PYGO1
    nsv6972459copy number variation1nstd229human GRCh38 chr15: 55,166,400-55,860,617 , GRCh37.p13 chr15: 55,458,598-56,152,815 RSL24D1, PIERCE2, 11 more genes
    nsv6969533copy number variation1nstd229human GRCh38 chr15: 55,550,230-55,556,612 , GRCh37.p13 chr15: 55,842,428-55,848,810 PYGO1
    nsv6966449copy number variation1nstd229human GRCh38 chr15: 55,533,547-55,540,006 , GRCh37.p13 chr15: 55,825,745-55,832,204 PYGO1
    nsv6963628copy number variation1nstd229human GRCh38 chr15: 55,550,229-55,553,499 , GRCh37.p13 chr15: 55,842,427-55,845,697 PYGO1
    nsv6962198copy number variation1nstd229human GRCh38 chr15: 55,051,495-55,683,909 , GRCh37.p13 chr15: 55,343,693-55,976,107 RSL24D1, MIR628, 11 more genes
    nsv6961121copy number variation1nstd229human GRCh38 chr15: 55,049,166-55,670,888 , GRCh37.p13 chr15: 55,341,364-55,963,086 PIGB, CCPG1, 11 more genes
    nsv6960840copy number variation1nstd229human GRCh38 chr15: 55,208,187-55,563,610 , GRCh37.p13 chr15: 55,500,385-55,855,808 MIR628, PIGB, 8 more genes
    nsv6637449copy number variation1nstd102humanUncertain significance GRCh37 chr15: 55,346,224-55,967,397 , GRCh38.p12 chr15: 55,054,026-55,675,199 PIERCE2, RSL24D1, 11 more genes
    nsv6637384copy number variation1nstd102humanPathogenic GRCh37 chr15: 48,589,845-63,543,438 , GRCh38.p12 chr15: 48,297,648-63,251,239 LINC03065, FAM227B, 228 more genes
    nsv6594972inversion1nstd223human GRCh38 chr15: 55,565,423-55,565,955 , GRCh37.p13 chr15: 55,857,621-55,858,153 PYGO1
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