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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv4457144copy number variation1nstd102humanUncertain significance GRCh37 chr6: 44,964,410-45,021,808 , GRCh38.p12 chr6: 44,996,673-45,054,071 SUPT3H
    nsv6312480copy number variation1nstd102humanPathogenic GRCh37 chr6: 45,296,464-45,480,154 , GRCh38.p12 chr6: 45,328,727-45,512,417 SUPT3H, RUNX2
    nsv7097433copy number variation1nstd102humanPathogenic GRCh37 chr6: 45,296,464-45,390,714 , GRCh38.p12 chr6: 45,328,727-45,422,977 SUPT3H, RUNX2
    nsv3878228copy number variation1nstd102humanPathogenic GRCh37 chr6: 45,308,920-45,413,885 , GRCh38 chr6: 45,341,183-45,446,148 SUPT3H, RUNX2
    nsv4455662copy number variation1nstd102humanPathogenic GRCh37 chr6: 45,325,590-45,406,397 , GRCh38.p12 chr6: 45,357,853-45,438,660 SUPT3H, RUNX2
    nsv4729337copy number variation1nstd102humanLikely benign GRCh37 chr6: 44,893,008-45,075,893 , GRCh38.p12 chr6: 44,925,271-45,108,156 SUPT3H, RBM22P4
    nsv3877854copy number variation1nstd102humanLikely benign GRCh37 chr6: 44,852,511-44,984,555 , GRCh38.p12 chr6: 44,884,774-45,016,818 SUPT3H, NUDT19P4
    nsv3888722copy number variation1nstd102humanBenign GRCh37 chr6: 45,294,400-45,404,528 , GRCh38.p12 chr6: 45,326,663-45,436,791 SUPT3H, RUNX2
    nsv3920908copy number variation1nstd102humanUncertain significance NCBI36 chr6: 44,945,718-45,148,858 , GRCh37.p13 chr6: 44,837,740-45,040,880 , GRCh38.p12 chr6: 44,870,003-45,073,143 SUPT3H, NUDT19P4
    nsv3924621copy number variation1nstd102humanUncertain significance NCBI36 chr6: 44,998,029-45,193,213 , GRCh37.p13 chr6: 44,890,051-45,085,235 , GRCh38.p12 chr6: 44,922,314-45,117,498 SUPT3H, RBM22P4
    nsv3919041copy number variation1nstd102humanUncertain significance NCBI36 chr6: 45,040,388-45,193,213 , GRCh37.p13 chr6: 44,932,410-45,085,235 , GRCh38.p12 chr6: 44,964,673-45,117,498 SUPT3H, RBM22P4
    nsv3876059copy number variation1nstd102humanconflicting data from submitters GRCh37 chr6: 45,319,017-45,383,847 , GRCh38.p12 chr6: 45,351,280-45,416,110 SUPT3H, RUNX2
    nsv5673768copy number variation1nstd102humanPathogenic GRCh37 chr6: 45,296,464-46,047,979 , GRCh38.p12 chr6: 45,328,727-46,080,242 SUPT3H, RNU6-754P, 3 more genes
    nsv5673682copy number variation1nstd102humanPathogenic GRCh37 chr6: 45,290,616-45,631,495 , GRCh38.p12 chr6: 45,322,879-45,663,758 SUPT3H, RUNX2, 1 more genes
    nsv3875077copy number variation1nstd102humanUncertain significance GRCh37 chr6: 44,861,183-45,082,967 , GRCh38.p12 chr6: 44,893,446-45,115,230 SUPT3H, NUDT19P4, 1 more genes
    nsv3920427copy number variation1nstd102humanUncertain significance GRCh37 chr6: 45,020,402-45,233,484 , GRCh38 chr6: 45,052,665-45,265,747 , NCBI36 chr6: 45,128,380-45,341,462 SUPT3H, MIR586, 2 more genes
    nsv3881993copy number variation1nstd102humanUncertain significance GRCh37 chr6: 45,325,578-45,590,330 , GRCh38.p12 chr6: 45,357,841-45,622,593 SUPT3H, RUNX2-AS1, 1 more genes
    nsv3877980copy number variation1nstd102humanPathogenic GRCh37 chr6: 44,988,031-45,626,855 , GRCh38.p12 chr6: 45,020,294-45,659,118 SUPT3H, RUNX2, 4 more genes
    nsv3919521copy number variation1nstd102humanPathogenic NCBI36 chr6: 37,853,123-45,729,558 , GRCh37 chr6: 37,745,145-45,621,580 , GRCh38 chr6: 37,777,369-45,653,843 SUPT3H, RPL23P6, 184 more genes
    nsv3884243copy number variation1nstd102humanPathogenic GRCh37 chr6: 43,636,308-50,947,320 , GRCh38.p12 chr6: 43,668,571-50,979,607 SUPT3H, GLYATL3, 105 more genes
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