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Items: 1 to 20 of 202

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7097916copy number variation1nstd102humanUncertain significance GRCh37 chr9: 102,988,324-103,062,956 , GRCh38.p12 chr9: 100,226,042-100,300,674 INVS, TEX10
    nsv7078062inversion1nstd229human GRCh38 chr9: 99,955,191-100,728,757 , GRCh37.p13 chr9: 102,717,473-103,491,039 CAVIN4, UPF3AP3, 13 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
    nsv7061246inversion1nstd229human GRCh38 chr9: 100,289,413-100,307,310 , GRCh37.p13 chr9: 103,051,695-103,069,592 TEX10, INVS
    nsv6876626copy number variation1nstd229human GRCh38 chr9: 100,339,115-100,374,229 , GRCh37.p13 chr9: 103,101,397-103,136,511 TEX10, LOC105376177
    nsv6876542copy number variation1nstd229human GRCh38 chr9: 100,314,502-100,317,120 , GRCh37.p13 chr9: 103,076,784-103,079,402 TEX10
    nsv6874110copy number variation1nstd229human GRCh38 chr9: 100,301,138-100,301,167 , GRCh37.p13 chr9: 103,063,420-103,063,449 TEX10, INVS
    nsv6871224copy number variation1nstd229human GRCh38 chr9: 100,310,801-100,348,600 , GRCh37.p13 chr9: 103,073,083-103,110,882 TEX10
    nsv6859556copy number variation1nstd229human GRCh38 chr9: 100,331,145-100,336,792 , GRCh37.p13 chr9: 103,093,427-103,099,074 TEX10
    nsv6859203copy number variation1nstd229human GRCh38 chr9: 100,344,523-100,356,867 , GRCh37.p13 chr9: 103,106,805-103,119,149 TEX10, LOC105376177
    nsv6634454copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-131,603,223 , GRCh38.p12 chr9: 203,861-128,840,944 HNRNPA1P41, GAS1RR, 1868 more genes
    nsv6569483inversion1nstd223human GRCh38 chr9: 100,313,260-100,314,357 , GRCh37.p13 chr9: 103,075,542-103,076,639 TEX10
    nsv6559869inversion1nstd223human GRCh38 chr9: 100,332,564-100,333,226 , GRCh37.p13 chr9: 103,094,846-103,095,508 TEX10
    nsv6558336inversion1nstd223human GRCh38 chr9: 99,955,191-100,728,759 , GRCh37.p13 chr9: 102,717,473-103,491,041 RPS2P35, STX17, 13 more genes
    nsv6441141copy number variation1nstd223human GRCh38 chr9: 100,329,654-100,330,119 , GRCh37.p13 chr9: 103,091,936-103,092,401 TEX10
    nsv6441102copy number variation1nstd223human GRCh38 chr9: 100,318,903-100,319,899 , GRCh37.p13 chr9: 103,081,185-103,082,181 TEX10
    nsv6437810copy number variation1nstd223human GRCh38 chr9: 100,321,201-100,322,500 , GRCh37.p13 chr9: 103,083,483-103,084,782 TEX10
    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
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