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Items: 1 to 20 of 376

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    nsv7077440inversion1nstd229human GRCh38 chr13: 95,324,680-102,597,006 , GRCh37.p13 chr13: 95,976,934-103,249,356 RN7SL60P, RPL15P18, 111 more genes
    nsv7074997inversion1nstd229human GRCh38 chr13: 97,451,643-97,456,714 , GRCh37.p13 chr13: 98,103,897-98,108,968 RAP2A
    nsv7074947inversion1nstd229human GRCh38 chr13: 97,456,273-97,456,713 , GRCh37.p13 chr13: 98,108,527-98,108,967 RAP2A
    nsv6948851copy number variation1nstd229human GRCh38 chr13: 97,451,642-97,456,154 , GRCh37.p13 chr13: 98,103,896-98,108,408 RAP2A
    nsv6946224copy number variation1nstd229human GRCh38 chr13: 97,451,601-97,455,100 , GRCh37.p13 chr13: 98,103,855-98,107,354 RAP2A
    nsv6938192copy number variation1nstd229human GRCh38 chr13: 97,458,551-97,459,292 , GRCh37.p13 chr13: 98,110,805-98,111,546 RAP2A
    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
    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
    nsv6593467inversion1nstd223human GRCh38 chr13: 97,469,422-97,469,753 , GRCh37.p13 chr13: 98,121,676-98,122,007 RAP2A
    nsv6592007inversion1nstd223human GRCh38 chr13: 97,451,641-97,456,712 , GRCh37.p13 chr13: 98,103,895-98,108,966 RAP2A
    nsv6586651inversion1nstd223human GRCh38 chr13: 97,456,271-97,456,713 , GRCh37.p13 chr13: 98,108,525-98,108,967 RAP2A
    nsv6580111inversion1nstd223human GRCh38 chr13: 97,469,291-97,469,870 , GRCh37.p13 chr13: 98,121,545-98,122,124 RAP2A
    nsv6492593copy number variation1nstd223human GRCh38 chr13: 97,455,201-97,456,100 , GRCh37.p13 chr13: 98,107,455-98,108,354 RAP2A
    nsv6492453copy number variation1nstd223human GRCh38 chr13: 97,451,601-97,454,700 , GRCh37.p13 chr13: 98,103,855-98,106,954 RAP2A
    nsv6492320copy number variation1nstd223human GRCh38 chr13: 97,451,177-97,451,676 , GRCh37.p13 chr13: 98,103,431-98,103,930 RAP2A
    nsv6489774copy number variation1nstd223human GRCh38 chr13: 97,452,701-97,456,100 , GRCh37.p13 chr13: 98,104,955-98,108,354 RAP2A
    nsv6489183copy number variation1nstd223human GRCh38 chr13: 97,454,101-97,455,300 , GRCh37.p13 chr13: 98,106,355-98,107,554 RAP2A
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