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Items: 1 to 20 of 268

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148253copy number variation1nstd102humanPathogenic GRCh38 chr8: 449,893-23,854,904 , GRCh37.p13 chr8: 399,893-23,712,417 ENTPD4, LOC100421446, 447 more genes
    nsv7148146copy number variation1nstd102humanPathogenic GRCh38 chr8: 12,721,809-30,183,737 , GRCh37.p13 chr8: 12,579,318-30,041,253 LOC101929028, RPL35P6, 274 more genes
    nsv7098901copy number variation1nstd102humanLikely pathogenic GRCh37 chr8: 21,925,038-26,372,195 , GRCh38.p12 chr8: 22,067,527-26,514,679 BMP1, POLR3D, 95 more genes
    nsv7073429inversion1nstd229human GRCh38 chr8: 22,689,880-24,095,801 , GRCh37.p13 chr8: 22,547,393-23,953,314 TNFRSF10B, RNU1-148P, 34 more genes
    nsv6854134copy number variation1nstd229human GRCh38 chr8: 23,326,730-23,336,564 , GRCh37.p13 chr8: 23,184,243-23,194,077 LOXL2-AS1, LOXL2
    nsv6849679copy number variation1nstd229human GRCh38 chr8: 23,341,401-23,345,200 , GRCh37.p13 chr8: 23,198,914-23,202,713 LOXL2-AS1, LOXL2
    nsv6844670copy number variation1nstd229human GRCh38 chr8: 23,287,140-23,460,413 , GRCh37.p13 chr8: 23,144,653-23,317,926 R3HCC1, LOXL2, 2 more genes
    nsv6842954copy number variation1nstd229human GRCh38 chr8: 22,958,501-23,751,500 , GRCh37.p13 chr8: 22,816,014-23,609,013 TNFRSF10B, RNU4-71P, 23 more genes
    nsv6841066copy number variation1nstd229human GRCh38 chr8: 23,351,324-23,358,326 , GRCh37.p13 chr8: 23,208,837-23,215,839 LOXL2, LOXL2-AS1
    nsv6634301complex substitution1nstd102humanPathogenic GRCh38.p12 chr8: 208,048-43,132,174 , GRCh37 chr8: 158,048-42,987,317 NAT1, NAT2, 758 more genes
    nsv6566867inversion1nstd223human GRCh38 chr8: 23,364,167-23,364,834 , GRCh37.p13 chr8: 23,221,680-23,222,347 LOXL2, LOXL2-AS1
    nsv6565031inversion1nstd223human GRCh38 chr8: 22,900,235-30,247,902 , GRCh37.p13 chr8: 22,757,748-30,105,418 LOC105379349, MIR6876, 140 more genes
    nsv6431148copy number variation1nstd223human GRCh38 chr8: 23,287,135-23,460,409 , GRCh37.p13 chr8: 23,144,648-23,317,922 LOXL2-AS1, LOXL2, 2 more genes
    nsv6429716copy number variation1nstd223human GRCh38 chr8: 22,969,514-24,288,515 , GRCh37.p13 chr8: 22,827,027-24,146,028 NKX3-1, LOC107984124, 27 more genes
    nsv6429459copy number variation1nstd223human GRCh38 chr8: 23,296,973-23,543,937 , GRCh37.p13 chr8: 23,154,486-23,401,450 LOXL2, SLC25A37, 4 more genes
    nsv6315449copy number variation1nstd102humanPathogenic GRCh37 chr8: 158,048-30,187,456 , GRCh38.p12 chr8: 208,048-30,329,940 LOC101928016, RPL23AP54, 568 more genes
    nsv6315323complex substitution1nstd102humanPathogenic GRCh38.p12 chr8: 208,048-43,164,161 , GRCh37 chr8: 158,048-43,019,304 NAT1, NAT2, 760 more genes
    nsv6315176copy number variation1nstd102humanPathogenic GRCh37 chr8: 19,779,604-26,531,980 , GRCh38.p12 chr8: 19,922,093-26,674,463 TNFRSF10C, TNFRSF10A, 121 more genes
    nsv6312718copy number variation2nstd102humanUncertain significance GRCh37 chr8: 21,900,440-23,564,111 , GRCh38.p12 chr8: 22,042,929-23,706,598 LOC105379327, RPL23AP55, 56 more genes
    nsv6245746mobile element insertion1nstd215human GRCh38 chr8: 23,342,204-23,342,204 , GRCh37.p13 chr8: 23,199,717-23,199,717 LOXL2-AS1, LOXL2
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