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Items: 1 to 20 of 139

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7147123copy number variation1nstd232human GRCh37.p13 chr9: 99,799,680-99,799,773 , GRCh38.p12 chr9: 97,037,398-97,037,491 CTSV
    nsv7075365inversion1nstd229human GRCh38 chr9: 94,549,389-100,549,990 , GRCh37.p13 chr9: 97,311,671-103,312,272 PCAT7, ANKS6, 128 more genes
    nsv6877577copy number variation1nstd229human GRCh38 chr9: 96,755,585-97,161,429 , GRCh37.p13 chr9: 99,517,867-99,923,711 ZNF782, YRDCP2, 15 more genes
    nsv6871350copy number variation1nstd229human GRCh38 chr9: 97,037,040-97,043,314 , GRCh37.p13 chr9: 99,799,322-99,805,596 CTSV
    nsv6869915copy number variation1nstd229human GRCh38 chr9: 97,032,256-97,043,608 , GRCh37.p13 chr9: 99,794,538-99,805,890 CTSV
    nsv6868548copy number variation1nstd229human GRCh38 chr9: 97,035,277-97,040,723 , GRCh37.p13 chr9: 99,797,559-99,803,005 CTSV
    nsv6860425copy number variation1nstd229human GRCh38 chr9: 97,029,630-97,029,727 , GRCh37.p13 chr9: 99,791,912-99,792,009 CTSV
    nsv6634454copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-131,603,223 , GRCh38.p12 chr9: 203,861-128,840,944 HNRNPA1P41, GAS1RR, 1868 more genes
    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
    nsv6436781copy number variation1nstd223human GRCh38 chr9: 97,037,034-97,043,313 , GRCh37.p13 chr9: 99,799,316-99,805,595 CTSV
    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
    nsv6173612copy number variation1nstd214human GRCh38 chr9: 97,036,025-97,036,109 , GRCh37.p13 chr9: 99,798,307-99,798,391 CTSV
    nsv6136854copy number variation1nstd213human GRCh37 chr9: 99,740,000-100,170,001 , GRCh38.p12 chr9: 96,977,718-97,407,719 SUGT1P4-STRA6LP-CCDC180, MFSD14CP, 19 more genes
    nsv5486636copy number variation1nstd206human GRCh38 chr9: 97,038,355-97,038,571 , GRCh37.p13 chr9: 99,800,637-99,800,853 CTSV
    nsv5381561copy number variation1nstd102humanPathogenic GRCh37 chr9: 97,834,573-107,199,088 , GRCh38.p12 chr9: 95,072,291-104,436,807 TBC1D2, ZNF782, 170 more genes
    nsv5372857translocation1nstd200human GRCh38 chr9: 97,039,551-97,039,551 , GRCh38 chr9: 97,039,483-97,039,483 , GRCh37.p13 chr9: 99,801,765-99,801,765 , GRCh37.p13 chr9: 99,801,833-99,801,833 CTSV
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