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Items: 1 to 20 of 317

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148249copy number variation1nstd102humanPathogenic GRCh38 chr6: 113,857,248-130,442,177 , GRCh37.p13 chr6: 114,178,427-130,763,322 TRDN-AS1, LOC100420743, 179 more genes
    nsv7054647inversion1nstd229human GRCh38 chr6: 125,609,155-134,343,808 , GRCh37.p13 chr6: 125,930,301-134,664,946 RPS12, TMEM244, 130 more genes
    nsv7053719inversion1nstd229human GRCh38 chr6: 125,606,974-134,343,957 , GRCh37.p13 chr6: 125,928,120-134,665,095 SNORD100, SLC18B1, 130 more genes
    nsv7046169inversion1nstd229human GRCh38 chr6: 129,271,276-130,554,936 , GRCh37.p13 chr6: 129,592,421-130,876,081 LOC105377999, ARHGAP18, 10 more genes
    nsv7038109inversion1nstd229human GRCh38 chr6: 125,606,921-134,343,957 , GRCh37.p13 chr6: 125,928,067-134,665,095 PTPRK-AS1, MED23, 130 more genes
    nsv6816765copy number variation1nstd229human GRCh38 chr6: 130,044,548-130,045,046 , GRCh37.p13 chr6: 130,365,693-130,366,191 L3MBTL3
    nsv6815295copy number variation1nstd229human GRCh38 chr6: 130,122,371-130,123,206 , GRCh37.p13 chr6: 130,443,516-130,444,351 L3MBTL3
    nsv6813836copy number variation1nstd229human GRCh38 chr6: 130,036,947-130,041,447 , GRCh37.p13 chr6: 130,358,092-130,362,592 L3MBTL3
    nsv6806364copy number variation1nstd229human GRCh38 chr6: 129,456,162-130,282,882 , GRCh37.p13 chr6: 129,777,307-130,604,027 LOC105377999, L3MBTL3, 7 more genes
    nsv6804196copy number variation1nstd229human GRCh38 chr6: 130,122,175-130,124,151 , GRCh37.p13 chr6: 130,443,320-130,445,296 L3MBTL3
    nsv6804005copy number variation1nstd229human GRCh38 chr6: 130,104,718-130,104,930 , GRCh37.p13 chr6: 130,425,863-130,426,075 L3MBTL3
    nsv6799722copy number variation1nstd229human GRCh38 chr6: 130,073,427-130,075,134 , GRCh37.p13 chr6: 130,394,572-130,396,279 L3MBTL3
    nsv6799240copy number variation1nstd229human GRCh38 chr6: 130,113,183-130,113,369 , GRCh37.p13 chr6: 130,434,328-130,434,514 L3MBTL3
    nsv6618860copy number variation1nstd223human GRCh38 chr6: 130,096,746-130,097,145 , GRCh37.p13 chr6: 130,417,891-130,418,290 L3MBTL3
    nsv6618381copy number variation1nstd223human GRCh38 chr6: 130,044,548-130,045,046 , GRCh37.p13 chr6: 130,365,693-130,366,191 L3MBTL3
    nsv6614655copy number variation1nstd223human GRCh38 chr6: 130,071,301-130,072,900 , GRCh37.p13 chr6: 130,392,446-130,394,045 L3MBTL3
    nsv6614341copy number variation1nstd223human GRCh38 chr6: 130,075,210-130,075,670 , GRCh37.p13 chr6: 130,396,355-130,396,815 L3MBTL3
    nsv6611975copy number variation1nstd223human GRCh38 chr6: 130,013,901-130,018,900 , GRCh37.p13 chr6: 130,335,046-130,340,045 L3MBTL3
    nsv6611028copy number variation1nstd223human GRCh38 chr6: 130,083,201-130,084,600 , GRCh37.p13 chr6: 130,404,346-130,405,745 L3MBTL3
    nsv6607716copy number variation1nstd223human GRCh38 chr6: 130,138,457-130,138,902 , GRCh37.p13 chr6: 130,459,602-130,460,047 L3MBTL3, SAMD3
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