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Items: 1 to 20 of 192

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7077729inversion1nstd229human GRCh38 chr9: 94,417,509-96,970,614 , GRCh37.p13 chr9: 97,179,791-99,732,896 HSD17B3-AS1, ERCC6L2, 60 more genes
    nsv7075365inversion1nstd229human GRCh38 chr9: 94,549,389-100,549,990 , GRCh37.p13 chr9: 97,311,671-103,312,272 PCAT7, ANKS6, 128 more genes
    nsv7066470inversion1nstd229human GRCh38 chr9: 94,557,471-94,557,577 , GRCh37.p13 chr9: 97,319,753-97,319,859 FBP2, PCAT7
    nsv6869224copy number variation1nstd229human GRCh38 chr9: 94,539,909-94,583,206 , GRCh37.p13 chr9: 97,302,191-97,345,488 PCAT7, FBP2
    nsv6869115copy number variation1nstd229human GRCh38 chr9: 94,551,333-94,587,973 , GRCh37.p13 chr9: 97,313,615-97,350,255 PCAT7, FBP2
    nsv6867018copy number variation1nstd229human GRCh38 chr9: 94,517,455-94,657,399 , GRCh37.p13 chr9: 97,279,737-97,419,681 FBP1, PCAT7, 1 more genes
    nsv6858124copy number variation1nstd229human GRCh38 chr9: 94,565,727-94,565,780 , GRCh37.p13 chr9: 97,328,009-97,328,062 PCAT7, FBP2
    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
    nsv6637673copy number variation1nstd102humanUncertain significance GRCh37 chr9: 97,281,155-97,456,120 , GRCh38.p12 chr9: 94,518,873-94,693,838 PCAT7, FBP2, 2 more genes
    nsv6637636copy number variation1nstd102humanUncertain significance GRCh37 chr9: 97,150,648-97,477,837 , GRCh38.p12 chr9: 94,388,366-94,715,555 PCAT7, FBP1, 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
    nsv6555716inversion1nstd223human GRCh38 chr9: 94,561,514-94,562,119 , GRCh37.p13 chr9: 97,323,796-97,324,401 FBP2, PCAT7
    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
    nsv6290004inversion1nstd102humanLikely pathogenic GRCh38.p12 chr9: 12,246,100-98,797,096 , GRCh37 chr9: 12,246,100-101,559,378 ACO1, PLIN2, 1215 more genes
    nsv6136851copy number variation1nstd213human GRCh37 chr9: 97,200,000-97,910,001 , GRCh38.p12 chr9: 94,437,718-95,147,719 MIR27B, MIR2278, 18 more genes
    nsv6097157insertion1nstd212human GRCh38 chr9: 94,557,254-94,557,254 , GRCh37.p13 chr9: 97,319,536-97,319,536 FBP2, PCAT7
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