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Items: 1 to 20 of 228

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7051246inversion1nstd229human GRCh38 chr2: 99,001,430-99,852,801 , GRCh37.p13 chr2: 99,617,893-100,469,263 EIF5B, MITD1, 12 more genes
    nsv7048300inversion1nstd229human GRCh38 chr2: 99,265,181-99,296,019 , GRCh37.p13 chr2: 99,881,644-99,912,482 LYG1
    nsv6693154copy number variation1nstd229human GRCh38 chr2: 99,257,501-99,338,800 , GRCh37.p13 chr2: 99,873,964-99,955,263 LYG1, LYG2, 3 more genes
    nsv6684630copy number variation1nstd229human GRCh38 chr2: 99,258,930-99,379,566 , GRCh37.p13 chr2: 99,875,393-99,996,029 EIF5B, LOC107985923, 3 more genes
    nsv6684457copy number variation1nstd229human GRCh38 chr2: 99,281,882-99,359,521 , GRCh37.p13 chr2: 99,898,345-99,975,984 LYG1, EIF5B, 2 more genes
    nsv6683227copy number variation1nstd229human GRCh38 chr2: 99,253,491-99,300,472 , GRCh37.p13 chr2: 99,869,954-99,916,935 LYG2, LYG1
    nsv6681330copy number variation1nstd229human GRCh38 chr2: 99,303,946-99,305,302 , GRCh37.p13 chr2: 99,920,409-99,921,765 TXNDC9, LYG1, 1 more genes
    nsv6681206copy number variation1nstd229human GRCh38 chr2: 99,177,793-99,328,393 , GRCh37.p13 chr2: 99,794,256-99,944,856 MRPL30, LYG1, 4 more genes
    nsv6636724copy number variation1nstd102humanUncertain significance GRCh37 chr2: 99,865,439-100,005,128 , GRCh38.p12 chr2: 99,248,976-99,388,665 LYG2, LYG1, 3 more genes
    nsv6636315copy number variation1nstd102humanLikely pathogenic GRCh37 chr2: 95,341,388-100,340,514 , GRCh38.p12 chr2: 94,675,663-99,724,052 ADRA2B, ATP5F1BP1, 130 more genes
    nsv6634330copy number variation1nstd102humanPathogenic GRCh37 chr2: 11,504,318-111,365,996 , GRCh38.p12 chr2: 11,364,192-110,608,419 CYP1B1-AS1, LOC107985771, 1649 more genes
    nsv6628610copy number variation5nstd224human GRCh37 chr2: 99,847,890-99,909,958 , GRCh38.p12 chr2: 99,231,427-99,293,495 LYG2, LYG1
    nsv6628432copy number variation1nstd224human GRCh37 chr2: 99,861,865-100,210,642 , GRCh38.p12 chr2: 99,245,402-99,594,180 AFF3, EIF5B, 5 more genes
    nsv6628184copy number variation1nstd224human GRCh37 chr2: 99,857,670-99,909,958 , GRCh38.p12 chr2: 99,241,207-99,293,495 LYG2, LYG1
    nsv6628183copy number variation2nstd224human GRCh37 chr2: 99,841,944-99,921,275 , GRCh38.p12 chr2: 99,225,481-99,304,812 LYG1, TXNDC9, 1 more genes
    nsv6554187inversion1nstd223human GRCh38 chr2: 99,288,696-99,289,341 , GRCh37.p13 chr2: 99,905,159-99,905,804 LYG1
    nsv6553571inversion1nstd223human GRCh38 chr2: 99,217,675-99,677,499 , GRCh37.p13 chr2: 99,834,138-100,293,961 AFF3, EIF5B, 5 more genes
    nsv6542558inversion1nstd223human GRCh38 chr2: 99,288,710-99,289,332 , GRCh37.p13 chr2: 99,905,173-99,905,795 LYG1
    nsv6349726copy number variation1nstd223human GRCh38 chr2: 99,302,863-99,304,404 , GRCh37.p13 chr2: 99,919,326-99,920,867 TXNDC9, LYG1
    nsv6343907copy number variation1nstd223human GRCh38 chr2: 99,303,812-99,304,213 , GRCh37.p13 chr2: 99,920,275-99,920,676 LYG1, TXNDC9
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