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Items: 1 to 20 of 171

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148269copy number variation1nstd102humanPathogenic GRCh38 chr8: 37,814,644-38,528,889 , GRCh37.p13 chr8: 37,672,162-38,386,407 GOT1L1, FGFR1, 20 more genes
    nsv7148130copy number variation1nstd102humanPathogenic GRCh37 chr8: 36,763,176-50,929,707 , GRCh38.p12 chr8: 36,905,658-50,017,147 SNTG1, RN7SL806P, 193 more genes
    nsv6853008copy number variation1nstd229human GRCh38 chr8: 37,839,586-37,846,726 , GRCh37.p13 chr8: 37,697,104-37,704,244 ADGRA2, BRF2
    nsv6850277copy number variation1nstd229human GRCh38 chr8: 37,819,401-37,869,600 , GRCh37.p13 chr8: 37,676,919-37,727,118 RAB11FIP1, ADGRA2, 1 more genes
    nsv6848712copy number variation1nstd229human GRCh38 chr8: 37,819,301-37,842,000 , GRCh37.p13 chr8: 37,676,819-37,699,518 BRF2, ADGRA2
    nsv6844298copy number variation1nstd229human GRCh38 chr8: 37,817,988-37,846,313 , GRCh37.p13 chr8: 37,675,506-37,703,831 BRF2, ADGRA2
    nsv6637025copy number variation1nstd102humanPathogenic GRCh37 chr8: 26,808,969-38,346,383 , GRCh38.p12 chr8: 26,951,452-38,488,865 LINC02948, LOC105379354, 185 more genes
    nsv6634301complex substitution1nstd102humanPathogenic GRCh38.p12 chr8: 208,048-43,132,174 , GRCh37 chr8: 158,048-42,987,317 NAT1, NAT2, 758 more genes
    nsv6427657copy number variation1nstd223human GRCh38 chr8: 37,848,238-37,852,036 , GRCh37.p13 chr8: 37,705,756-37,709,554 BRF2
    nsv6315323complex substitution1nstd102humanPathogenic GRCh38.p12 chr8: 208,048-43,164,161 , GRCh37 chr8: 158,048-43,019,304 NAT1, NAT2, 760 more genes
    nsv6312909copy number variation5nstd102humanUncertain significance, Pathogenic GRCh37 chr8: 37,595,441-38,961,219 , GRCh38.p12 chr8: 37,737,923-39,103,700 LSM1, BAG4, 33 more genes
    nsv6291079copy number variation1nstd102humanUncertain significance GRCh37 chr8: 37,544,476-37,818,465 , GRCh38.p12 chr8: 37,686,958-37,960,947 ZNF703, BRF2, 10 more genes
    nsv6137281copy number variation1nstd213human GRCh37 chr8: 37,350,000-38,410,001 , GRCh38.p12 chr8: 37,492,482-38,552,483 ADRB3, EIF4EBP1, 32 more genes
    nsv6136578copy number variation1nstd213human GRCh37 chr8: 37,570,000-37,710,001 , GRCh38.p12 chr8: 37,712,482-37,852,483 ERLIN2, PLPBP, 6 more genes
    nsv5922137copy number variation1nstd209human GRCh38 chr8: 37,848,197-37,852,054 , GRCh37.p13 chr8: 37,705,715-37,709,572 BRF2
    nsv5861047copy number variation1nstd209human GRCh38 chr8: 37,848,231-37,852,105 , GRCh37.p13 chr8: 37,705,749-37,709,623 BRF2
    nsv5484907copy number variation1nstd206human GRCh38 chr8: 37,843,499-37,843,549 , GRCh37.p13 chr8: 37,701,017-37,701,067 ADGRA2, BRF2
    nsv5200364copy number variation1nstd102humanPathogenic GRCh37 chr8: 176,814-43,396,776 , GRCh38.p12 chr8: 226,814-43,541,633 LOC100130612, XPO7, 770 more genes
    nsv4954352copy number variation1nstd200human GRCh38 chr8: 37,817,988-37,846,347 , GRCh37.p13 chr8: 37,675,506-37,703,865 ADGRA2, BRF2
    nsv4827417copy number variation1nstd200human GRCh37 chr8: 37,706,004-37,709,531 , GRCh38.p12 chr8: 37,848,486-37,852,013 BRF2
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