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Items: 1 to 20 of 133

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7067178inversion1nstd229human GRCh38 chr9: 78,097,080-78,097,872 , GRCh37.p13 chr9: 80,711,996-80,712,788 LOC107987031
    nsv6876803copy number variation1nstd229human GRCh38 chr9: 78,092,400-78,146,422 , GRCh37.p13 chr9: 80,707,316-80,761,338 LOC107987031
    nsv6870229copy number variation1nstd229human GRCh38 chr9: 78,090,967-78,095,338 , GRCh37.p13 chr9: 80,705,883-80,710,254 LOC107987031
    nsv6866794copy number variation1nstd229human GRCh38 chr9: 78,094,881-78,095,046 , GRCh37.p13 chr9: 80,709,797-80,709,962 LOC107987031
    nsv6865898copy number variation1nstd229human GRCh38 chr9: 78,091,501-78,093,200 , GRCh37.p13 chr9: 80,706,417-80,708,116 LOC107987031
    nsv6863671copy number variation1nstd229human GRCh38 chr9: 78,096,930-78,331,884 , GRCh37.p13 chr9: 80,711,846-80,946,800 RN7SKP59, SYNGR2P2, 6 more genes
    nsv6858421copy number variation1nstd229human GRCh38 chr9: 77,965,302-78,341,298 , GRCh37.p13 chr9: 80,580,218-80,956,214 LOC107987031, PSAT1, 7 more genes
    nsv6637642copy number variation1nstd102humanUncertain significance GRCh37 chr9: 80,582,026-80,948,266 , GRCh38.p12 chr9: 77,967,110-78,333,350 GNAQ, LOC107987082, 7 more genes
    nsv6634454copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-131,603,223 , GRCh38.p12 chr9: 203,861-128,840,944 HNRNPA1P41, GAS1RR, 1868 more genes
    nsv6634017copy number variation1nstd224human GRCh37 chr9: 80,704,731-80,881,659 , GRCh38.p12 chr9: 78,089,815-78,266,743 CEP78, SYNGR2P2, 5 more genes
    nsv6572847inversion1nstd223human GRCh38 chr9: 78,095,551-78,095,655 , GRCh37.p13 chr9: 80,710,467-80,710,571 LOC107987031
    nsv6568042inversion1nstd223human GRCh38 chr9: 77,399,209-87,276,767 , GRCh37.p13 chr9: 80,014,125-89,891,682 , LOC105376119, 118 more genes
    nsv6560453inversion1nstd223human GRCh38 chr9: 78,095,532-78,096,068 , GRCh37.p13 chr9: 80,710,448-80,710,984 LOC107987031
    nsv6557715inversion1nstd223human GRCh38 chr9: 75,901,418-82,872,806 , GRCh37.p13 chr9: 78,516,334-85,487,721 , LOC105376096, 79 more genes
    nsv6555963inversion1nstd223human GRCh38 chr9: 78,097,240-78,097,342 , GRCh37.p13 chr9: 80,712,156-80,712,258 LOC107987031
    nsv6453240copy number variation1nstd223human GRCh38 chr9: 78,092,399-78,146,421 , GRCh37.p13 chr9: 80,707,315-80,761,337 LOC107987031
    nsv6315405copy number variation1nstd102humanUncertain significance GRCh37 chr9: 19,356,861-119,513,311 , GRCh38.p12 chr9: 19,356,863-116,751,032 RNU6-156P, GDA, 1425 more genes
    nsv6313900copy number variation1nstd102humanLikely pathogenic GRCh37 chr9: 71,349,994-122,603,410 , GRCh38.p12 chr9: 68,735,078-119,841,132 ABCA1, ALAD, 793 more genes
    nsv6313827copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-84,155,399 , GRCh38.p12 chr9: 203,861-81,540,484 RPSAP75, ANKRD20A2P, 1008 more genes
    nsv6313546copy number variation1nstd102humanPathogenic GRCh37 chr9: 353,349-141,020,389 , GRCh38.p12 chr9: 353,349-138,125,937 FAM27C, DPM2, 2166 more genes
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