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Items: 1 to 20 of 929

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148238copy number variation1nstd102humanPathogenic GRCh38 chr8: 115,586,904-135,607,135 , GRCh37.p13 chr8: 116,599,131-136,619,378 CCDC26, EFR3A, 238 more genes
    nsv7148132copy number variation1nstd102humanPathogenic GRCh37 chr8: 131,138,343-143,473,913 , GRCh38.p12 chr8: 130,126,097-142,392,552 LOC107983985, MIR30DHG, 104 more genes
    nsv7098160copy number variation1nstd102humanUncertain significance GRCh37 chr8: 133,141,509-133,175,761 , GRCh38.p12 chr8: 132,129,262-132,163,514 KCNQ3
    nsv7097786copy number variation1nstd102humanUncertain significance GRCh37 chr8: 133,492,374-133,492,779 , GRCh38.p12 chr8: 132,480,127-132,480,532 KCNQ3
    nsv7093098copy number variation1nstd102humanUncertain significance GRCh37 chr8: 133,492,703-133,492,753 , GRCh38 chr8: 132,480,456-132,480,506 KCNQ3
    nsv7077533inversion1nstd229human GRCh38 chr8: 125,245,829-133,039,076 , GRCh37.p13 chr8: 126,258,071-134,051,321 PVT1, MTRF1LP2, 76 more genes
    nsv7069943inversion1nstd229human GRCh38 chr8: 132,254,954-132,257,405 , GRCh37.p13 chr8: 133,267,201-133,269,652 KCNQ3
    nsv7064413inversion1nstd229human GRCh38 chr8: 132,426,904-132,426,943 , GRCh37.p13 chr8: 133,439,151-133,439,190 KCNQ3
    nsv7062365inversion1nstd229human GRCh38 chr8: 131,355,985-132,586,379 , GRCh37.p13 chr8: 132,368,232-133,598,626 EFR3A, HHLA1, 8 more genes
    nsv7060057inversion1nstd229human GRCh38 chr8: 132,396,955-132,396,976 , GRCh37.p13 chr8: 133,409,202-133,409,223 KCNQ3
    nsv6857998copy number variation1nstd229human GRCh38 chr8: 132,262,956-132,265,665 , GRCh37.p13 chr8: 133,275,203-133,277,912 KCNQ3
    nsv6857687copy number variation1nstd229human GRCh38 chr8: 132,469,843-132,478,587 , GRCh37.p13 chr8: 133,482,090-133,490,834 KCNQ3
    nsv6857318copy number variation1nstd229human GRCh38 chr8: 126,364,525-132,576,581 , GRCh37.p13 chr8: 127,376,770-133,588,829 PRNCR1, MIR1205, 59 more genes
    nsv6857067copy number variation1nstd229human GRCh38 chr8: 132,176,580-132,177,151 , GRCh37.p13 chr8: 133,188,827-133,189,398 KCNQ3
    nsv6856353copy number variation1nstd229human GRCh38 chr8: 132,187,701-132,187,952 , GRCh37.p13 chr8: 133,199,948-133,200,199 KCNQ3
    nsv6856054copy number variation1nstd229human GRCh38 chr8: 132,309,501-132,318,700 , GRCh37.p13 chr8: 133,321,748-133,330,947 KCNQ3
    nsv6855888copy number variation1nstd229human GRCh38 chr8: 132,374,231-132,389,158 , GRCh37.p13 chr8: 133,386,478-133,401,405 KCNQ3
    nsv6855636copy number variation1nstd229human GRCh38 chr8: 132,389,944-132,392,598 , GRCh37.p13 chr8: 133,402,191-133,404,845 KCNQ3
    nsv6854784copy number variation1nstd229human GRCh38 chr8: 132,332,098-132,334,883 , GRCh37.p13 chr8: 133,344,345-133,347,130 KCNQ3
    nsv6854485copy number variation1nstd229human GRCh38 chr8: 132,376,692-132,385,948 , GRCh37.p13 chr8: 133,388,939-133,398,195 KCNQ3
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