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Items: 1 to 20 of 643

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137211copy number variation1nstd102humanPathogenic GRCh37 chr10: 11,138,692-135,427,143 , GRCh38.p12 chr10: 11,096,729-133,613,639 EXOC6, VCL, 1906 more genes
    nsv7137209copy number variation1nstd102humanPathogenic GRCh37 chr10: 12,829,206-135,427,143 , GRCh38.p12 chr10: 12,787,207-133,613,639 RNU7-12P, RNU1-65P, 1876 more genes
    nsv7098887copy number variation1nstd102humanPathogenic GRCh37 chr10: 93,249,133-97,616,970 , GRCh38.p12 chr10: 91,489,376-95,857,213 LGI1, LOC107984257, 79 more genes
    nsv7077195inversion1nstd229human GRCh38 chr10: 93,320,010-93,320,149 , GRCh37.p13 chr10: 95,079,767-95,079,906 MYOF
    nsv7072503inversion1nstd229human GRCh38 chr10: 93,434,812-93,455,326 , GRCh37.p13 chr10: 95,194,569-95,215,083 MYOF
    nsv7064816inversion1nstd229human GRCh38 chr10: 93,451,148-93,451,245 , GRCh37.p13 chr10: 95,210,905-95,211,002 MYOF
    nsv7059501inversion1nstd229human GRCh38 chr10: 93,437,131-93,437,236 , GRCh37.p13 chr10: 95,196,888-95,196,993 MYOF
    nsv6896497copy number variation1nstd229human GRCh38 chr10: 93,393,631-93,397,421 , GRCh37.p13 chr10: 95,153,388-95,157,178 MYOF
    nsv6895846copy number variation1nstd229human GRCh38 chr10: 93,385,759-93,392,968 , GRCh37.p13 chr10: 95,145,516-95,152,725 MYOF
    nsv6895459copy number variation1nstd229human GRCh38 chr10: 93,479,139-93,482,780 , GRCh37.p13 chr10: 95,238,896-95,242,537 MYOF
    nsv6895333copy number variation1nstd229human GRCh38 chr10: 93,477,265-93,480,325 , GRCh37.p13 chr10: 95,237,022-95,240,082 MYOF
    nsv6894481copy number variation1nstd229human GRCh38 chr10: 93,326,904-93,327,784 , GRCh37.p13 chr10: 95,086,661-95,087,541 MYOF
    nsv6893326copy number variation1nstd229human GRCh38 chr10: 93,425,894-93,438,988 , GRCh37.p13 chr10: 95,185,651-95,198,745 MYOF
    nsv6893119copy number variation1nstd229human GRCh38 chr10: 93,357,701-93,360,000 , GRCh37.p13 chr10: 95,117,458-95,119,757 MYOF
    nsv6892354copy number variation1nstd229human GRCh38 chr10: 93,330,814-93,331,007 , GRCh37.p13 chr10: 95,090,571-95,090,764 MYOF
    nsv6892148copy number variation1nstd229human GRCh38 chr10: 93,374,118-93,378,719 , GRCh37.p13 chr10: 95,133,875-95,138,476 MYOF
    nsv6891660copy number variation1nstd229human GRCh38 chr10: 93,314,066-93,314,459 , GRCh37.p13 chr10: 95,073,823-95,074,216 MYOF
    nsv6890277copy number variation1nstd229human GRCh38 chr10: 92,959,667-93,311,724 , GRCh37.p13 chr10: 94,719,424-95,071,481 MYOF, RPL17P34, 5 more genes
    nsv6889405copy number variation1nstd229human GRCh38 chr10: 93,384,852-93,395,120 , GRCh37.p13 chr10: 95,144,609-95,154,877 MYOF
    nsv6888033copy number variation1nstd229human GRCh38 chr10: 93,448,831-93,451,752 , GRCh37.p13 chr10: 95,208,588-95,211,509 MYOF
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