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Items: 1 to 20 of 314

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137123copy number variation1nstd102humanPathogenic GRCh37 chr8: 89,179,899-97,978,274 , GRCh38.p12 chr8: 88,167,670-96,966,046 SLC26A7, LOC105375639, 112 more genes
    nsv7136994copy number variation1nstd102humanUncertain significance GRCh38 chr8: 89,971,145-89,971,146 , GRCh37 chr8: 90,983,373-90,983,374 NBN
    nsv7098186copy number variation1nstd102humanUncertain significance GRCh37 chr8: 90,955,471-90,996,789 , GRCh38.p12 chr8: 89,943,243-89,984,561 NBN
    nsv7098185copy number variation1nstd102humanLikely pathogenic GRCh37 chr8: 90,955,471-90,958,533 , GRCh38.p12 chr8: 89,943,243-89,946,305 NBN
    nsv7098040copy number variation1nstd102humanUncertain significance GRCh37 chr8: 90,982,582-90,996,789 , GRCh38.p12 chr8: 89,970,354-89,984,561 NBN
    nsv7097912copy number variation1nstd102humanPathogenic GRCh37 chr8: 90,960,042-90,976,745 , GRCh38.p12 chr8: 89,947,814-89,964,517 NBN
    nsv7097911copy number variation1nstd102humanUncertain significance GRCh37 chr8: 90,947,810-90,976,745 , GRCh38.p12 chr8: 89,935,582-89,964,517 NBN, OSGIN2
    nsv7097671copy number variation1nstd102humanLikely pathogenic GRCh37 chr8: 90,947,810-90,960,130 , GRCh38.p12 chr8: 89,935,582-89,947,902 OSGIN2, NBN
    nsv7097670copy number variation1nstd102humanUncertain significance GRCh37 chr8: 90,947,810-90,958,533 , GRCh38.p12 chr8: 89,935,582-89,946,305 OSGIN2, NBN
    nsv7093509insertion1nstd102humanPathogenic GRCh37 chr8: 90,982,766-90,982,766 , GRCh38 chr8: 89,970,538-89,970,538 NBN
    nsv7078060inversion1nstd229human GRCh38 chr8: 88,934,395-91,030,131 , GRCh37.p13 chr8: 89,946,624-92,042,359 RNA5SP273, LOC105375631, 21 more genes
    nsv6857698copy number variation1nstd229human GRCh38 chr8: 89,506,124-90,615,140 , GRCh37.p13 chr8: 90,518,353-91,627,368 LOC107986955, RNU6-925P, 12 more genes
    nsv6856576copy number variation1nstd229human GRCh38 chr8: 89,975,110-89,981,175 , GRCh37.p13 chr8: 90,987,338-90,993,403 NBN
    nsv6855560copy number variation1nstd229human GRCh38 chr8: 89,928,286-89,963,475 , GRCh37.p13 chr8: 90,940,514-90,975,703 NBN, OSGIN2
    nsv6854048copy number variation1nstd229human GRCh38 chr8: 89,932,191-89,941,896 , GRCh37.p13 chr8: 90,944,419-90,954,124 OSGIN2, NBN
    nsv6848493copy number variation1nstd229human GRCh38 chr8: 89,948,219-89,948,385 , GRCh37.p13 chr8: 90,960,447-90,960,613 NBN
    nsv6847790copy number variation1nstd229human GRCh38 chr8: 89,981,179-89,981,676 , GRCh37.p13 chr8: 90,993,407-90,993,904 NBN
    nsv6843863copy number variation1nstd229human GRCh38 chr8: 89,944,793-89,951,260 , GRCh37.p13 chr8: 90,957,021-90,963,488 NBN
    nsv6842420copy number variation1nstd229human GRCh38 chr8: 89,940,754-89,967,859 , GRCh37.p13 chr8: 90,952,982-90,980,087 NBN
    nsv6842117copy number variation1nstd229human GRCh38 chr8: 89,934,358-89,934,553 , GRCh37.p13 chr8: 90,946,586-90,946,781 NBN, OSGIN2
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