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Items: 1 to 20 of 222

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7099226copy number variation1nstd231human GRCh38.p12 chr1: 115,063,638-119,984,872 , GRCh37 chr1: 115,606,259-120,527,495 ATP1A1, CASQ2, 103 more genes
    nsv7047008inversion1nstd229human GRCh38 chr1: 117,025,879-117,031,369 , GRCh37.p13 chr1: 117,568,501-117,573,991 CD101-AS1, CD101
    nsv6640703copy number variation1nstd229human GRCh38 chr1: 117,032,001-117,045,400 , GRCh37.p13 chr1: 117,574,623-117,588,022 CD101, CD101-AS1
    nsv6640702copy number variation1nstd229human GRCh38 chr1: 117,022,616-117,025,692 , GRCh37.p13 chr1: 117,565,238-117,568,314 CD101-AS1, CD101
    nsv6640664copy number variation1nstd229human GRCh38 chr1: 117,022,629-117,030,298 , GRCh37.p13 chr1: 117,565,251-117,572,920 CD101-AS1, CD101
    nsv6640591copy number variation1nstd229human GRCh38 chr1: 117,012,953-117,014,788 , GRCh37.p13 chr1: 117,555,575-117,557,410 CD101
    nsv6640487copy number variation1nstd229human GRCh38 chr1: 117,008,926-117,021,735 , GRCh37.p13 chr1: 117,551,548-117,564,357 CD101
    nsv6640486copy number variation1nstd229human GRCh38 chr1: 116,988,401-117,000,900 , GRCh37.p13 chr1: 117,531,023-117,543,522 PTGFRN, CD101
    nsv6640485copy number variation1nstd229human GRCh38 chr1: 116,936,483-117,173,099 , GRCh37.p13 chr1: 117,479,105-117,715,721 CD101, CD101-AS1, 7 more genes
    nsv6640484copy number variation1nstd229human GRCh38 chr1: 116,933,801-117,004,500 , GRCh37.p13 chr1: 117,476,423-117,547,122 RNA5SP55, CD101, 1 more genes
    nsv6625102copy number variation1nstd224human GRCh37 chr1: 117,524,022-117,675,943 , GRCh38.p12 chr1: 116,981,400-117,133,321 PTGFRN, TTF2, 4 more genes
    nsv6543196inversion1nstd223human GRCh38 chr1: 117,007,521-117,008,194 , GRCh37.p13 chr1: 117,550,143-117,550,816 CD101
    nsv6332639copy number variation1nstd223human GRCh38 chr1: 117,030,195-117,043,685 , GRCh37.p13 chr1: 117,572,817-117,586,307 CD101-AS1, CD101
    nsv6313671copy number variation1nstd102humanPathogenic GRCh37 chr1: 111,647,582-121,343,783 , GRCh38.p12 chr1: 111,104,960-121,601,985 GAPDHP23, RNA5SP56, 243 more genes
    nsv6226764insertion1nstd214human GRCh38 chr1: 117,029,229-117,029,229 , GRCh37.p13 chr1: 117,571,851-117,571,851 CD101, CD101-AS1
    nsv6167250copy number variation1nstd214human GRCh38 chr1: 117,029,129-117,029,218 , GRCh37.p13 chr1: 117,571,751-117,571,840 CD101, CD101-AS1
    nsv6165894copy number variation1nstd214human GRCh38 chr1: 117,029,180-117,029,256 , GRCh37.p13 chr1: 117,571,802-117,571,878 CD101, CD101-AS1
    nsv6165285copy number variation1nstd214human GRCh38 chr1: 117,029,129-117,029,214 , GRCh37.p13 chr1: 117,571,751-117,571,836 CD101-AS1, CD101
    nsv6163710copy number variation1nstd214human GRCh38 chr1: 117,029,131-117,029,212 , GRCh37.p13 chr1: 117,571,753-117,571,834 CD101, CD101-AS1
    nsv6157104copy number variation1nstd214human GRCh38 chr1: 117,029,200-117,029,256 , GRCh37.p13 chr1: 117,571,822-117,571,878 CD101, CD101-AS1
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