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Items: 1 to 20 of 248

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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
    nsv6856363copy number variation1nstd229human GRCh38 chr8: 23,424,738-23,427,691 , GRCh37.p13 chr8: 23,282,251-23,285,204 ENTPD4
    nsv6856196copy number variation1nstd229human GRCh38 chr8: 23,455,101-23,526,200 , GRCh37.p13 chr8: 23,312,614-23,383,713 ENTPD4, LOC646708, 1 more genes
    nsv6855871copy number variation1nstd229human GRCh38 chr8: 23,452,001-23,587,300 , GRCh37.p13 chr8: 23,309,514-23,444,813 ENTPD4, SLC25A37, 2 more genes
    nsv6855515copy number variation1nstd229human GRCh38 chr8: 23,446,335-23,498,598 , GRCh37.p13 chr8: 23,303,848-23,356,111 LOC646708, ENTPD4, 1 more genes
    nsv6855497copy number variation1nstd229human GRCh38 chr8: 23,435,243-23,438,372 , GRCh37.p13 chr8: 23,292,756-23,295,885 ENTPD4
    nsv6854682copy number variation1nstd229human GRCh38 chr8: 23,457,292-23,457,318 , GRCh37.p13 chr8: 23,314,805-23,314,831 ENTPD4
    nsv6850799copy number variation1nstd229human GRCh38 chr8: 23,379,671-23,441,673 , GRCh37.p13 chr8: 23,237,184-23,299,186 ENTPD4, LOXL2
    nsv6848661copy number variation1nstd229human GRCh38 chr8: 23,437,002-23,441,997 , GRCh37.p13 chr8: 23,294,515-23,299,510 ENTPD4
    nsv6847066copy number variation1nstd229human GRCh38 chr8: 23,443,727-23,451,449 , GRCh37.p13 chr8: 23,301,240-23,308,962 ENTPD4
    nsv6846161copy number variation1nstd229human GRCh38 chr8: 23,457,352-23,457,362 , GRCh37.p13 chr8: 23,314,865-23,314,875 ENTPD4
    nsv6846044copy number variation1nstd229human GRCh38 chr8: 23,442,053-23,446,238 , GRCh37.p13 chr8: 23,299,566-23,303,751 ENTPD4
    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
    nsv6842034copy number variation1nstd229human GRCh38 chr8: 23,441,298-23,444,294 , GRCh37.p13 chr8: 23,298,811-23,301,807 ENTPD4
    nsv6634301complex substitution1nstd102humanPathogenic GRCh38.p12 chr8: 208,048-43,132,174 , GRCh37 chr8: 158,048-42,987,317 NAT1, NAT2, 758 more genes
    nsv6565031inversion1nstd223human GRCh38 chr8: 22,900,235-30,247,902 , GRCh37.p13 chr8: 22,757,748-30,105,418 LOC105379349, MIR6876, 140 more genes
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