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Items: 1 to 20 of 962

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7145132copy number variation1nstd232human GRCh37.p13 chr2: 137,647,874-137,647,973 , GRCh38.p12 chr2: 136,890,304-136,890,403 THSD7B
    nsv7138156insertion1nstd232human GRCh37.p13 chr2: 138,245,304-138,245,304 , GRCh38.p12 chr2: 137,487,734-137,487,734 THSD7B
    nsv7137604copy number variation1nstd232human GRCh37.p13 chr2: 138,088,687-138,088,764 , GRCh38.p12 chr2: 137,331,117-137,331,194 THSD7B
    nsv7057981inversion1nstd229human GRCh38 chr2: 136,855,428-136,859,593 , GRCh37.p13 chr2: 137,612,998-137,617,163 THSD7B
    nsv7057869inversion1nstd229human GRCh38 chr2: 137,335,414-137,335,438 , GRCh37.p13 chr2: 138,092,984-138,093,008 THSD7B
    nsv7054317inversion1nstd229human GRCh38 chr2: 137,008,624-137,017,243 , GRCh37.p13 chr2: 137,766,194-137,774,813 THSD7B
    nsv7053007inversion1nstd229human GRCh38 chr2: 137,055,289-137,056,389 , GRCh37.p13 chr2: 137,812,859-137,813,959 THSD7B
    nsv7052573inversion1nstd229human GRCh38 chr2: 137,288,359-137,292,173 , GRCh37.p13 chr2: 138,045,929-138,049,743 THSD7B
    nsv7051258inversion1nstd229human GRCh38 chr2: 136,840,044-136,979,979 , GRCh37.p13 chr2: 137,597,614-137,737,549 THSD7B
    nsv7048049inversion1nstd229human GRCh38 chr2: 136,785,445-136,801,801 , GRCh37.p13 chr2: 137,543,015-137,559,371 THSD7B
    nsv7045739inversion1nstd229human GRCh38 chr2: 137,584,112-137,585,397 , GRCh37.p13 chr2: 138,341,682-138,342,967 THSD7B
    nsv7044395inversion1nstd229human GRCh38 chr2: 136,820,052-136,820,128 , GRCh37.p13 chr2: 137,577,622-137,577,698 THSD7B
    nsv7044174inversion1nstd229human GRCh38 chr2: 137,474,160-137,474,190 , GRCh37.p13 chr2: 138,231,730-138,231,760 THSD7B
    nsv7044080inversion1nstd229human GRCh38 chr2: 136,783,750-142,804,814 , GRCh37.p13 chr2: 137,541,320-143,562,383 LOC105373634, LOC107985822, 42 more genes
    nsv7040933inversion1nstd229human GRCh38 chr2: 137,485,587-137,490,739 , GRCh37.p13 chr2: 138,243,157-138,248,309 THSD7B
    nsv7039858inversion1nstd229human GRCh38 chr2: 136,782,605-136,800,584 , GRCh37.p13 chr2: 137,540,175-137,558,154 THSD7B
    nsv7038853inversion1nstd229human GRCh38 chr2: 136,921,818-136,936,535 , GRCh37.p13 chr2: 137,679,388-137,694,105 THSD7B
    nsv6697927copy number variation1nstd229human GRCh38 chr2: 136,844,542-136,844,641 , GRCh37.p13 chr2: 137,602,112-137,602,211 THSD7B
    nsv6697886copy number variation1nstd229human GRCh38 chr2: 137,285,563-137,286,094 , GRCh37.p13 chr2: 138,043,133-138,043,664 THSD7B
    nsv6697832copy number variation1nstd229human GRCh38 chr2: 137,307,159-137,330,213 , GRCh37.p13 chr2: 138,064,729-138,087,783 THSD7B
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