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Items: 1 to 20 of 290

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148239copy number variation1nstd102humanPathogenic GRCh38 chr13: 98,343,655-110,990,677 , GRCh37.p13 chr13: 98,995,909-111,643,024 CLYBL-AS3, PPIAP24, 162 more genes
    nsv7098899copy number variation1nstd102humanPathogenic GRCh37 chr13: 95,675,427-105,286,434 , GRCh38.p12 chr13: 95,023,173-104,634,083 PCCA, LOC105370340, 131 more genes
    nsv7094414copy number variation1nstd102humanPathogenic GRCh37 chr13: 99,336,978-102,379,160 , GRCh38.p12 chr13: 98,684,724-101,726,810 MIR623, UBAC2-AS1, 51 more genes
    nsv7094230copy number variation3nstd102humanUncertain significance GRCh37 chr13: 100,038,233-103,718,599 , GRCh38.p12 chr13: 99,385,979-103,066,249 CLYBL-AS3, LOC107984615, 59 more genes
    nsv7077440inversion1nstd229human GRCh38 chr13: 95,324,680-102,597,006 , GRCh37.p13 chr13: 95,976,934-103,249,356 RN7SL60P, RPL15P18, 111 more genes
    nsv7072178inversion1nstd229human GRCh38 chr13: 97,997,035-104,548,310 , GRCh37.p13 chr13: 98,649,289-105,200,661 RNU1-24P, DOCK9, 95 more genes
    nsv7065401inversion1nstd229human GRCh38 chr13: 99,559,949-99,560,032 , GRCh37.p13 chr13: 100,212,203-100,212,286 TM9SF2
    nsv6955184copy number variation1nstd229human GRCh38 chr13: 99,298,801-101,250,600 , GRCh37.p13 chr13: 99,951,055-101,902,951 PCCA-DT, HMGB3P4, 36 more genes
    nsv6948910copy number variation1nstd229human GRCh38 chr13: 99,564,298-99,580,986 , GRCh37.p13 chr13: 100,216,552-100,233,240 LINC01039, TM9SF2, 1 more genes
    nsv6948420copy number variation1nstd229human GRCh38 chr13: 99,527,341-99,535,750 , GRCh37.p13 chr13: 100,179,595-100,188,004 RNY3P6, TM9SF2
    nsv6947151copy number variation1nstd229human GRCh38 chr13: 99,502,729-99,504,716 , GRCh37.p13 chr13: 100,154,983-100,156,970 TM9SF2
    nsv6945682copy number variation1nstd229human GRCh38 chr13: 99,513,179-99,556,448 , GRCh37.p13 chr13: 100,165,433-100,208,702 RNY3P6, TM9SF2
    nsv6942893copy number variation1nstd229human GRCh38 chr13: 99,501,831-99,501,898 , GRCh37.p13 chr13: 100,154,085-100,154,152 TM9SF2
    nsv6941509copy number variation1nstd229human GRCh38 chr13: 99,538,583-99,538,991 , GRCh37.p13 chr13: 100,190,837-100,191,245 TM9SF2
    nsv6940420copy number variation1nstd229human GRCh38 chr13: 99,504,525-99,515,800 , GRCh37.p13 chr13: 100,156,779-100,168,054 TM9SF2
    nsv6638047copy number variation1nstd102humanPathogenic GRCh37 chr13: 75,268,539-115,107,733 , GRCh38.p12 chr13: 74,694,402-114,342,258 CUL4A, LOC105370373, 488 more genes
    nsv6637615copy number variation1nstd102humanPathogenic GRCh37 chr13: 93,535,335-105,788,229 , GRCh38.p12 chr13: 92,883,082-105,135,878 SNORD13G, FTLP8, 162 more genes
    nsv6637400copy number variation1nstd102humanPathogenic GRCh37 chr13: 97,142,120-115,107,733 , GRCh38.p12 chr13: 96,489,866-114,342,258 LOC107984609, LINC00354, 265 more genes
    nsv6637217copy number variation1nstd102humanPathogenic GRCh37 chr13: 99,421,603-115,107,733 , GRCh38.p12 chr13: 98,769,349-114,342,258 LOC107984609, CLYBL-AS2, 231 more genes
    nsv6634431copy number variation1nstd102humanPathogenic GRCh37 chr13: 19,253,848-115,108,937 , GRCh38.p12 chr13: 18,679,708-114,343,462 MTUS2-AS1, LOC105370213, 1330 more genes
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