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Items: 1 to 20 of 194

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5947137copy number variation1nstd209human GRCh38 chr12: 48,056,140-48,056,195 , GRCh37.p13 chr12: 48,449,923-48,449,978 SENP1
    nsv5935574copy number variation1nstd209human GRCh38 chr12: 48,056,588-48,056,773 , GRCh37.p13 chr12: 48,450,371-48,450,556 SENP1
    nsv5932884copy number variation1nstd209human GRCh38 chr12: 48,105,909-48,119,824 , GRCh37.p13 chr12: 48,499,692-48,513,607 PFKM, SENP1
    nsv5664068insertion1nstd207human GRCh38 chr12: 48,056,848-48,056,848 , GRCh37.p13 chr12: 48,450,631-48,450,631 SENP1
    nsv5603537copy number variation1nstd207human GRCh38 chr12: 48,056,490-48,056,634 , GRCh37.p13 chr12: 48,450,273-48,450,417 SENP1
    nsv5594517copy number variation1nstd207human GRCh38 chr12: 48,056,490-48,056,547 , GRCh37.p13 chr12: 48,450,273-48,450,330 SENP1
    nsv5586945copy number variation1nstd207human GRCh38 chr12: 48,056,709-48,056,945 , GRCh37.p13 chr12: 48,450,492-48,450,728 SENP1
    nsv5564512copy number variation1nstd102humanLikely pathogenic GRCh37 chr12: 37,873,948-49,578,619 , GRCh38.p12 chr12: 37,480,146-49,184,836 ADCY6, ABCD2, 187 more genes
    nsv5534843insertion1nstd206human GRCh38 chr12: 48,078,333-48,078,372 , GRCh37.p13 chr12: 48,472,116-48,472,155 SENP1
    nsv5499711copy number variation1nstd206human GRCh38 chr12: 48,041,915-48,042,054 , GRCh37.p13 chr12: 48,435,698-48,435,837 SENP1
    nsv5380901copy number variation1nstd102humanUncertain significance GRCh37 chr12: 48,240,430-48,539,491 , GRCh38.p12 chr12: 47,846,647-48,145,708 LOC105369750, SENP1, 9 more genes
    nsv5379723translocation1nstd200human GRCh38 chr12: 48,061,215-48,061,215 , GRCh38 chr12: 48,062,166-48,062,166 , GRCh37.p13 chr12: 48,455,949-48,455,949 , GRCh37.p13 chr12: 48,454,998-48,454,998 SENP1
    nsv5040224inversion1nstd200human GRCh38 chr12: 47,213,128-71,357,206 , GRCh37.p13 chr12: 47,606,911-71,750,986 , NR4A1, 686 more genes
    nsv5029954inversion1nstd200human GRCh38 chr12: 38,328,571-48,487,625 , GRCh37.p13 chr12: 38,722,373-48,881,408 , MESDP1, 138 more genes
    nsv4972510copy number variation1nstd200human GRCh38 chr12: 48,102,445-48,104,203 , GRCh37.p13 chr12: 48,496,228-48,497,986 SENP1, PFKM
    nsv4842064copy number variation1nstd200human GRCh37 chr12: 48,435,698-48,435,837 , GRCh38.p12 chr12: 48,041,915-48,042,054 SENP1
    nsv4759166insertion1nstd199human GRCh37 chr12: 48,472,106-48,472,106 , GRCh38.p12 chr12: 48,078,323-48,078,323 SENP1
    nsv4755205inversion1nstd199human GRCh37 chr12: 25,956,127-125,801,151 , GRCh38.p12 chr12: 25,803,193-125,316,605 , ACACB, 1787 more genes
    nsv4744625copy number variation1nstd199human GRCh37 chr12: 48,450,199-48,450,565 , GRCh38.p12 chr12: 48,056,416-48,056,782 SENP1
    nsv4736781copy number variation1nstd199human GRCh37 chr12: 25,957,322-125,801,148 , GRCh38.p12 chr12: 25,804,388-125,316,602 , RNA5SP368, 1787 more genes
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