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Items: 1 to 20 of 143

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5973346inversion1nstd209human GRCh38 chr12: 118,054,601-123,705,841 , GRCh37.p13 chr12: 118,492,406-124,190,388 , ACADS, 162 more genes
    nsv5651499insertion1nstd207human GRCh38 chr12: 120,467,991-120,467,991 , GRCh37.p13 chr12: 120,905,794-120,905,794 SRSF9, DYNLL1
    nsv5273593copy number variation1nstd204human GRCh38.p13 chr12: 120,426,401-120,552,600 , GRCh37.p13 chr12: 120,864,204-120,990,403 , SRSF9, 9 more genes
    nsv5137603mobile element insertion1nstd203human GRCh38 chr12: 120,467,969-120,467,996 , GRCh37.p13 chr12: 120,905,772-120,905,799 SRSF9, DYNLL1
    nsv5136825mobile element insertion1nstd203human GRCh38 chr12: 120,467,972-120,467,996 , GRCh37.p13 chr12: 120,905,775-120,905,799 SRSF9, DYNLL1
    nsv5133620mobile element insertion1nstd203human GRCh38 chr12: 120,467,993-120,467,996 , GRCh37.p13 chr12: 120,905,796-120,905,799 DYNLL1, SRSF9
    nsv5133352mobile element insertion1nstd203human GRCh38 chr12: 120,467,992-120,467,996 , GRCh37.p13 chr12: 120,905,795-120,905,799 DYNLL1, SRSF9
    nsv5128606mobile element insertion1nstd203human GRCh38 chr12: 120,467,976-120,467,993 , GRCh37.p13 chr12: 120,905,779-120,905,796 DYNLL1, SRSF9
    nsv5128321mobile element insertion1nstd203human GRCh38 chr12: 120,467,995-120,467,995 , GRCh37.p13 chr12: 120,905,798-120,905,798 DYNLL1, SRSF9
    nsv5127917mobile element insertion1nstd203human GRCh38 chr12: 120,467,977-120,467,994 , GRCh37.p13 chr12: 120,905,780-120,905,797 DYNLL1, SRSF9
    nsv5126300mobile element insertion1nstd203human GRCh38 chr12: 120,467,994-120,467,996 , GRCh37.p13 chr12: 120,905,797-120,905,799 SRSF9, DYNLL1
    nsv5125288mobile element insertion1nstd203human GRCh38 chr12: 120,467,987-120,467,996 , GRCh37.p13 chr12: 120,905,790-120,905,799 SRSF9, DYNLL1
    nsv5122898mobile element insertion1nstd203human GRCh38 chr12: 120,467,970-120,467,972 , GRCh37.p13 chr12: 120,905,773-120,905,775 SRSF9, DYNLL1
    nsv5121116mobile element insertion1nstd203human GRCh38 chr12: 120,467,968-120,467,996 , GRCh37.p13 chr12: 120,905,771-120,905,799 SRSF9, DYNLL1
    nsv5120691mobile element insertion1nstd203human GRCh38 chr12: 120,468,231-120,468,231 , GRCh37.p13 chr12: 120,906,034-120,906,034 SRSF9, DYNLL1
    nsv5120164mobile element insertion1nstd203human GRCh38 chr12: 120,467,991-120,467,996 , GRCh37.p13 chr12: 120,905,794-120,905,799 SRSF9, DYNLL1
    nsv4993757copy number variation1nstd200human GRCh38 chr12: 120,439,940-120,461,480 , GRCh37.p13 chr12: 120,877,743-120,899,283 TRIAP1, RPL31P52, 3 more genes
    nsv4768524insertion1nstd186human GRCh37 chr12: 120,905,795-120,905,795 , GRCh38.p12 chr12: 120,467,992-120,467,992 DYNLL1, SRSF9
    nsv4756208inversion1nstd199human GRCh37 chr12: 104,359,633-125,801,147 , GRCh38.p12 chr12: 103,965,855-125,316,601 , ACACB, 453 more genes
    nsv4755205inversion1nstd199human GRCh37 chr12: 25,956,127-125,801,151 , GRCh38.p12 chr12: 25,803,193-125,316,605 , ACACB, 1787 more genes
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