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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3067375insertion1nstd90human GRCh37 (hg19) chr15: 25,118,736-25,118,737 , GRCh38 (hg38) chr15: 24,873,589-24,873,590 SNRPN
    nsv3064688insertion1nstd140human GRCh38 (hg38) chr15: 24,892,544-24,892,545 , GRCh37 (hg19) chr15: 25,137,691-25,137,692 SNRPN
    nsv2795024insertion1nstd137human GRCh38 (hg38) chr15: 24,848,259-24,848,259 , GRCh37 (hg19) chr15: 25,093,406-25,093,406 SNRPN
    nsv2794927copy number variation1nstd137human GRCh38 (hg38) chr15: 24,834,949-24,835,060 , GRCh37 (hg19) chr15: 25,080,096-25,080,207 SNRPN
    nsv2794841copy number variation1nstd137human GRCh38 (hg38) chr15: 24,871,847-24,873,589 , GRCh37 (hg19) chr15: 25,116,994-25,118,736 SNRPN
    nsv2794174insertion1nstd137human GRCh38 (hg38) chr15: 24,919,085-24,919,085 , GRCh37 (hg19) chr15: 25,164,232-25,164,232 SNRPN
    nsv2794173insertion1nstd137human GRCh38 (hg38) chr15: 24,892,576-24,892,576 , GRCh37 (hg19) chr15: 25,137,723-25,137,723 SNRPN
    nsv2784306copy number variation1nstd132human NCBI36 (hg18) chr15: 22,639,308-22,677,106 , GRCh37 (hg19) chr15: 25,088,215-25,126,013 , GRCh38 (hg38) chr15: 24,843,068-24,880,866 SNRPN
    nsv2783681copy number variation1nstd132human NCBI36 (hg18) chr15: 22,639,308-22,666,219 , GRCh37 (hg19) chr15: 25,088,215-25,115,126 , GRCh38 (hg38) chr15: 24,843,068-24,869,979 SNRPN
    nsv2782040copy number variation2nstd132human NCBI36 (hg18) chr15: 22,643,359-22,666,219 , GRCh37 (hg19) chr15: 25,092,266-25,115,126 , GRCh38 (hg38) chr15: 24,847,119-24,869,979 SNRPN
    nsv2781955complex chromosomal rearrangement2nstd133human GRCh37 (hg19) chr5: 69,441,340-69,441,340 , GRCh37 (hg19) chr5: 69,449,059-69,449,059 , GRCh37 (hg19) chr15: 25,121,931-25,121,931 , GRCh37 (hg19) chr15: 25,122,267-25,122,267 , GRCh38 (hg38) chr15: 24,876,784-24,876,784 , GRCh38 (hg38) chr15: 24,877,120-24,877,120 , GRCh38 (hg38) chr5: 70,145,513-70,145,513 , GRCh38 (hg38) chr5: 70,153,232-70,153,232 , GRCh38 (hg38) chr5|NT_187651.1: 378,596-378,596 , GRCh38 (hg38) chr5|NT_187651.1: 370,870-370,870 SNRPN
    nsv2781869complex chromosomal rearrangement2nstd133human GRCh37 (hg19) chr10: 120,586,180-120,586,180 , GRCh37 (hg19) chr10: 120,586,182-120,586,182 , GRCh37 (hg19) chr15: 25,219,251-25,219,251 , GRCh37 (hg19) chr15: 25,219,251-25,219,251 , GRCh38 (hg38) chr10: 118,826,668-118,826,668 , GRCh38 (hg38) chr10: 118,826,670-118,826,670 , GRCh38 (hg38) chr15: 24,974,104-24,974,104 , GRCh38 (hg38) chr15: 24,974,104-24,974,104 SNRPN, SNURF
    esv4006076copy number variation1estd231human GRCh37 (hg19) chr15: 25,115,703-25,117,504 , GRCh38 (hg38) chr15: 24,870,556-24,872,357 SNRPN
    nsv2779140copy number variation1nstd37humanPathogenic NCBI36 (hg18) chr15: 21,173,967-100,338,915 , GRCh37 (hg19) chr15: 23,622,526-102,521,392 , GRCh38 (hg38) chr15: 23,377,379-101,981,189 NR2E3, SNORD116-1, 877 more genes
    nsv2779135copy number variation1nstd37humanLikely pathogenic GRCh37 (hg19) chr15: 23,615,769-28,953,483 , GRCh38 (hg38) chr15: 23,370,622-28,708,337 , NCBI36 (hg18) chr15: 21,167,210-26,752,524 SNORD116-1, SNORD116-2, 121 more genes
    nsv2778895copy number variation2nstd37humanPathogenic GRCh37 (hg19) chr15: 22,770,421-28,545,355 , GRCh38 (hg38) chr15: 22,358,243-28,300,209 , GRCh38.p2 chr15|NW_011332701.1: 1-4,542,614 , NCBI36 (hg18) chr15: 20,321,785-26,218,950 SNORD116-1, SNORD116-2, 125 more genes
    nsv2778890copy number variation1nstd37humanUncertain significance NCBI36 (hg18) chr15: 22,633,599-22,670,019 , GRCh37 (hg19) chr15: 25,082,506-25,118,926 , GRCh38 (hg38) chr15: 24,837,359-24,873,779 SNRPN
    nsv2778805copy number variation1nstd37humanPathogenic GRCh37 (hg19) chr15: 22,770,421-33,707,835 , GRCh38 (hg38) chr15: 22,358,243-33,415,634 , NCBI36 (hg18) chr15: 20,321,785-31,495,127 SNORD116-1, SNORD116-2, 168 more genes
    nsv2778726copy number variation1nstd37humanPathogenic GRCh37 (hg19) chr15: 22,770,421-28,828,168 , GRCh38.p2 chr15|NW_011332701.1: 1-4,542,614 , GRCh38 (hg38) chr15: 22,358,243-28,583,022 , NCBI36 (hg18) chr15: 20,321,785-26,627,209 SNORD116-1, SNORD116-2, 129 more genes
    nsv2778617copy number variation1nstd37humanPathogenic GRCh37 (hg19) chr15: 22,770,421-28,419,123 , GRCh38 (hg38) chr15: 22,358,243-28,173,977 , GRCh38.p2 chr15|NW_011332701.1: 1-4,542,614 , NCBI36 (hg18) chr15: 20,321,785-26,092,718 SNORD116-1, SNORD116-2, 125 more genes
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