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Items: 1 to 20 of 112

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv4456871copy number variation1nstd102humanPathogenic GRCh37 chr8: 39,555,657-64,049,089 , GRCh38.p12 chr8: 39,698,138-63,136,530 CRIPTOP5, TRIM60P15, 297 more genes
    nsv4456811copy number variation1nstd102humanPathogenic GRCh37 chr8: 31,936,551-146,295,771 , GRCh38.p12 chr8: 32,079,035-145,070,385 TERF1, LOC107986945, 1511 more genes
    nsv4455349copy number variation1nstd102humanUncertain significance GRCh37 chr8: 57,699,846-58,315,215 , GRCh38.p12 chr8: 56,787,287-57,402,656 LINC00588, LOC286177, 7 more genes
    nsv4349554copy number variation2nstd102humanPathogenic GRCh37 chr8: 158,048-146,295,771 , GRCh38.p12 chr8: 208,048-145,070,385 LOC101929488, TEX15, 2105 more genes
    nsv4318272inversion1nstd166human GRCh37.p13 chr8: 51,271,211-76,167,888 , GRCh38.p12 chr8: 50,358,651-75,255,653 , ASPH, 341 more genes
    nsv4170863copy number variation1nstd166human GRCh37.p13 chr8: 57,826,965-57,837,574 , GRCh38.p12 chr8: 56,914,406-56,925,015 RNU6-13P
    nsv3924755copy number variation1nstd102humanPathogenic NCBI36 chr8: 50,546,890-58,900,583 , GRCh37 chr8: 50,384,337-58,738,029 , GRCh38 chr8: 49,471,778-57,825,470 LOC105375849, RP1, 103 more genes
    nsv3923517copy number variation1nstd102humanPathogenic NCBI36 chr8: 36,556,779-60,694,111 , GRCh37 chr8: 36,437,621-60,531,557 , GRCh38 chr8: 36,580,103-59,618,998 LOC105379380, TPT1P8, 320 more genes
    nsv3923501copy number variation1nstd102humanPathogenic NCBI36 chr8: 55,896,471-62,221,415 , GRCh38 chr8: 54,821,357-61,146,302 , GRCh37 chr8: 55,733,917-62,058,861 NUDT15P1, LINC01301, 83 more genes
    nsv3923310copy number variation1nstd102humanPathogenic NCBI36 chr8: 166,452-146,264,902 , GRCh38 chr8: 226,452-145,068,712 , GRCh37 chr8: 176,452-146,294,098 LOC112268023, RPL23AP96, 2105 more genes
    nsv3919904copy number variation1nstd102humanUncertain significance NCBI36 chr8: 57,295,657-58,077,274 , GRCh37 chr8: 57,133,103-57,914,720 , GRCh38 chr8: 56,220,544-57,002,161 LOC105375851, SEPTIN10P1, 13 more genes
    nsv3919282copy number variation1nstd102humanPathogenic GRCh37 chr8: 191,530-146,280,020 , GRCh38 chr8: 241,530-145,054,634 , NCBI36 chr8: 181,530-146,250,824 MIR4662B, LOC101927845, 2104 more genes
    nsv3919200copy number variation1nstd102humanPathogenic GRCh38 chr8: 241,530-145,049,449 , GRCh37 chr8: 191,530-146,274,835 , NCBI36 chr8: 181,530-146,245,639 LOC112268023, LOC105375925, 2103 more genes
    nsv3919101copy number variation1nstd102humanPathogenic GRCh38 chr8: 55,423,413-58,836,753 , NCBI36 chr8: 56,498,527-59,911,866 , GRCh37 chr8: 56,335,973-59,749,312 RPL37P6, RN7SL323P, 59 more genes
    nsv3919070copy number variation1nstd102humanPathogenic NCBI36 chr8: 54,569,654-58,566,126 , GRCh37.p13 chr8: 54,407,101-58,403,572 , GRCh38.p12 chr8: 53,494,541-57,491,013 BPNT2, RNU6-13P, 73 more genes
    nsv3916777copy number variation1nstd102humanPathogenic GRCh37 chr8: 158,048-146,295,771 , GRCh38 chr8: 208,048-145,070,385 , NCBI36 chr8: 148,048-146,266,575 RPL5P22, ARHGEF10, 2105 more genes
    nsv3916768copy number variation1nstd102humanPathogenic NCBI36 chr8: 47,062,121-70,378,576 , GRCh37 chr8: 46,942,956-70,216,022 , GRCh38 chr8: 46,031,334-69,303,787 RPL7L1P18, LINC03018, 316 more genes
    nsv3916438copy number variation1nstd102humanPathogenic GRCh37 chr8: 46,942,962-140,297,737 , NCBI36 chr8: 47,062,127-140,366,919 , GRCh38 chr8: 46,031,340-139,285,494 NDUFS5P6, LINC01289, 1152 more genes
    nsv3915762copy number variation1nstd102humanPathogenic NCBI36 chr8: 21,193,313-146,266,575 , GRCh38 chr8: 21,291,522-145,070,385 , GRCh37 chr8: 21,149,033-146,295,771 LOC105375693, MIR124-2HG, 1718 more genes
    nsv3915173copy number variation1nstd102humanPathogenic NCBI36 chr8: 3,938-146,274,826 , GRCh37.p13 chr8: 13,938-146,304,022 , GRCh38.p12 chr8: 63,938-145,078,636 RN7SL474P, UNC5D, 2109 more genes
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