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Items: 1 to 20 of 980

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6688190copy number variation1nstd229human GRCh38 chr2: 109,203,952-109,215,068 , GRCh37.p13 chr2: 109,820,408-109,831,524 SH3RF3
    nsv6694524copy number variation1nstd229human GRCh38 chr2: 109,382,012-109,390,878 , GRCh37.p13 chr2: 109,998,468-110,007,334 SH3RF3
    nsv6693201copy number variation1nstd229human GRCh38 chr2: 109,267,313-109,274,435 , GRCh37.p13 chr2: 109,883,769-109,890,891 SH3RF3
    nsv6691207copy number variation1nstd229human GRCh38 chr2: 109,182,022-109,188,708 , GRCh37.p13 chr2: 109,798,478-109,805,164 SH3RF3
    nsv6690129copy number variation1nstd229human GRCh38 chr2: 109,465,669-109,472,058 , GRCh37.p13 chr2: 110,082,125-110,088,514 SH3RF3
    nsv6688493copy number variation1nstd229human GRCh38 chr2: 109,402,504-109,408,867 , GRCh37.p13 chr2: 110,018,960-110,025,323 SH3RF3
    nsv6695913copy number variation1nstd229human GRCh38 chr2: 109,150,015-109,155,390 , GRCh37.p13 chr2: 109,766,471-109,771,846 SH3RF3
    nsv6681106copy number variation1nstd229human GRCh38 chr2: 109,143,766-109,149,043 , GRCh37.p13 chr2: 109,760,222-109,765,499 SH3RF3
    nsv6692927copy number variation1nstd229human GRCh38 chr2: 109,414,260-109,418,882 , GRCh37.p13 chr2: 110,030,716-110,035,338 SH3RF3
    nsv6697352copy number variation1nstd229human GRCh38 chr2: 109,326,687-109,331,228 , GRCh37.p13 chr2: 109,943,143-109,947,684 SH3RF3
    nsv6678966copy number variation1nstd229human GRCh38 chr2: 109,285,019-109,289,092 , GRCh37.p13 chr2: 109,901,475-109,905,548 SH3RF3
    nsv6688822copy number variation1nstd229human GRCh38 chr2: 109,348,787-109,352,788 , GRCh37.p13 chr2: 109,965,243-109,969,244 SH3RF3
    nsv6679814copy number variation1nstd229human GRCh38 chr2: 109,219,165-109,223,066 , GRCh37.p13 chr2: 109,835,621-109,839,522 SH3RF3
    nsv6685072copy number variation1nstd229human GRCh38 chr2: 109,187,512-109,191,339 , GRCh37.p13 chr2: 109,803,968-109,807,795 SH3RF3
    nsv6695426copy number variation1nstd229human GRCh38 chr2: 109,264,502-109,268,096 , GRCh37.p13 chr2: 109,880,958-109,884,552 SH3RF3
    nsv6694824copy number variation1nstd229human GRCh38 chr2: 109,408,816-109,411,736 , GRCh37.p13 chr2: 110,025,272-110,028,192 SH3RF3
    nsv6695916copy number variation1nstd229human GRCh38 chr2: 109,302,601-109,305,500 , GRCh37.p13 chr2: 109,919,057-109,921,956 SH3RF3
    nsv6685866copy number variation1nstd229human GRCh38 chr2: 109,440,230-109,443,102 , GRCh37.p13 chr2: 110,056,686-110,059,558 SH3RF3
    nsv6681010copy number variation1nstd229human GRCh38 chr2: 109,204,468-109,207,325 , GRCh37.p13 chr2: 109,820,924-109,823,781 SH3RF3
    nsv6697998copy number variation1nstd229human GRCh38 chr2: 109,149,578-109,152,221 , GRCh37.p13 chr2: 109,766,034-109,768,677 SH3RF3
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