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Items: 1 to 20 of 1727

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3909745copy number variation1nstd102humanBenign GRCh37 chr13: 96,915,624-96,932,945 , GRCh38.p12 chr13: 96,263,370-96,280,691 HS6ST3
    nsv3903785copy number variation1nstd102humanBenign GRCh37 chr13: 96,921,643-96,925,553 , GRCh38.p12 chr13: 96,269,389-96,273,299 HS6ST3
    nsv3901853copy number variation1nstd102humanBenign GRCh37 chr13: 96,742,250-96,743,232 , GRCh38.p12 chr13: 96,089,996-96,090,978 HS6ST3
    nsv3900712copy number variation1nstd102humanBenign GRCh37 chr13: 96,742,334-96,743,232 , GRCh38.p12 chr13: 96,090,080-96,090,978 HS6ST3
    nsv6291742copy number variation1nstd102humanUncertain significance GRCh37 chr13: 97,339,914-97,531,013 , GRCh38.p12 chr13: 96,687,660-96,878,759 HS6ST3
    nsv507727sequence alteration3nstd49human NCBI35 chr13: 95,609,247-95,615,247 , GRCh37.p13 chr13: 96,811,246-96,817,246 , GRCh38.p12 chr13: 96,158,992-96,164,992 HS6ST3
    nsv6945968copy number variation1nstd229human GRCh38 chr13: 96,431,071-96,537,047 , GRCh37.p13 chr13: 97,083,325-97,189,301 HS6ST3
    nsv6944241copy number variation1nstd229human GRCh38 chr13: 96,679,028-96,740,805 , GRCh37.p13 chr13: 97,331,282-97,393,059 HS6ST3
    nsv6948695copy number variation1nstd229human GRCh38 chr13: 96,667,401-96,727,400 , GRCh37.p13 chr13: 97,319,655-97,379,654 HS6ST3
    nsv6946434copy number variation1nstd229human GRCh38 chr13: 96,238,647-96,277,723 , GRCh37.p13 chr13: 96,890,901-96,929,977 HS6ST3
    nsv6949294copy number variation1nstd229human GRCh38 chr13: 96,773,298-96,807,839 , GRCh37.p13 chr13: 97,425,552-97,460,093 HS6ST3
    nsv6955281copy number variation1nstd229human GRCh38 chr13: 96,756,372-96,788,977 , GRCh37.p13 chr13: 97,408,626-97,441,231 HS6ST3
    nsv6950040copy number variation1nstd229human GRCh38 chr13: 96,301,604-96,331,147 , GRCh37.p13 chr13: 96,953,858-96,983,401 HS6ST3
    nsv6953140copy number variation1nstd229human GRCh38 chr13: 96,699,301-96,728,400 , GRCh37.p13 chr13: 97,351,555-97,380,654 HS6ST3
    nsv6942946copy number variation1nstd229human GRCh38 chr13: 96,652,289-96,679,641 , GRCh37.p13 chr13: 97,304,543-97,331,895 HS6ST3
    nsv6941132copy number variation1nstd229human GRCh38 chr13: 96,300,601-96,324,500 , GRCh37.p13 chr13: 96,952,855-96,976,754 HS6ST3
    nsv6949174copy number variation1nstd229human GRCh38 chr13: 96,593,634-96,617,169 , GRCh37.p13 chr13: 97,245,888-97,269,423 HS6ST3
    nsv6945969copy number variation1nstd229human GRCh38 chr13: 96,729,586-96,752,271 , GRCh37.p13 chr13: 97,381,840-97,404,525 HS6ST3
    nsv6956957copy number variation1nstd229human GRCh38 chr13: 96,605,672-96,623,168 , GRCh37.p13 chr13: 97,257,926-97,275,422 HS6ST3
    nsv6942155copy number variation1nstd229human GRCh38 chr13: 96,662,014-96,678,584 , GRCh37.p13 chr13: 97,314,268-97,330,838 HS6ST3
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