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Items: 1 to 20 of 137

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6876619copy number variation1nstd229human GRCh38 chr9: 94,268,921-94,438,687 , GRCh37.p13 chr9: 97,031,203-97,200,969 PTMAP12, MFSD14B, 7 more genes
    nsv6869310copy number variation1nstd229human GRCh38 chr9: 94,236,591-94,478,286 , GRCh37.p13 chr9: 96,998,873-97,240,568 LOC105376154, LOC107987023, 8 more genes
    nsv6637944copy number variation1nstd102humanPathogenic GRCh37 chr9: 95,711,603-98,469,214 , GRCh38.p12 chr9: 92,949,321-95,706,932 MIRLET7D, MIR24-1, 60 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
    nsv6633500copy number variation1nstd224human GRCh37 chr9: 96,973,995-97,228,918 , GRCh38.p12 chr9: 94,211,713-94,466,636 MFSD14B, LINC02603, 8 more genes
    nsv6452895copy number variation1nstd223human GRCh38 chr9: 94,346,701-94,348,700 , GRCh37.p13 chr9: 97,108,983-97,110,982 LOC100132077, PTMAP12
    nsv6447755copy number variation1nstd223human GRCh38 chr9: 92,901,749-100,255,234 , GRCh37.p13 chr9: 95,664,031-103,017,516 EIF4BP3, VN1R51P, 162 more genes
    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
    nsv6315179copy number variation1nstd102humanPathogenic GRCh37 chr9: 93,864,974-106,661,581 , GRCh38.p12 chr9: 91,102,692-103,899,300 SUGT1P4-STRA6LP, NR4A3, 255 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
    nsv6313546copy number variation1nstd102humanPathogenic GRCh37 chr9: 353,349-141,020,389 , GRCh38.p12 chr9: 353,349-138,125,937 FAM27C, DPM2, 2166 more genes
    nsv6303530copy number variation1nstd186human GRCh37 chr9: 97,097,834-97,110,834 , GRCh38.p12 chr9: 94,335,552-94,348,552 PTMAP12, LOC100132077, 1 more genes
    nsv6302425copy number variation1nstd186human GRCh37 chr9: 97,080,282-97,114,834 , GRCh38.p12 chr9: 94,318,000-94,352,552 NUTM2F, PTMAP12, 3 more genes
    nsv6290004inversion1nstd102humanLikely pathogenic GRCh38.p12 chr9: 12,246,100-98,797,096 , GRCh37 chr9: 12,246,100-101,559,378 ACO1, PLIN2, 1215 more genes
    nsv6142655copy number variation1nstd206human GRCh38 chr9: 94,335,552-94,348,552 , GRCh37.p13 chr9: 97,097,834-97,110,834 LOC100132077, LOC107987023, 1 more genes
    nsv6142511copy number variation1nstd206human GRCh38 chr9: 94,340,526-94,351,800 , GRCh37.p13 chr9: 97,102,808-97,114,082 LOC100132077, LOC107987023, 1 more genes
    nsv6141907copy number variation1nstd206human GRCh38 chr9: 94,334,239-94,346,552 , GRCh37.p13 chr9: 97,096,521-97,108,834 LOC100132077, LOC107987023, 1 more genes
    nsv6110822inversion1nstd212human GRCh38 chr9: 94,266,137-94,527,227 , GRCh37.p13 chr9: 97,028,419-97,289,509 NUTM2F, MFSD14B, 10 more genes
    nsv6018296copy number variation1nstd212human GRCh38 chr9: 94,345,835-94,346,709 , GRCh37.p13 chr9: 97,108,117-97,108,991 PTMAP12, LOC100132077
    nsv5492240copy number variation1nstd206human GRCh38 chr9: 94,318,000-94,352,552 , GRCh37.p13 chr9: 97,080,282-97,114,834 PTMAP12, LOC105376154, 3 more genes
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