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Items: 1 to 20 of 180

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6712385copy number variation1nstd229human GRCh38 chr3: 66,065,527-73,237,527 , GRCh37.p13 chr3: 66,051,202-73,286,678 , RNA5SP136, 79 more genes
    nsv6700936copy number variation1nstd229human GRCh38 chr3: 69,026,673-69,026,721 , GRCh37.p13 chr3: 69,075,824-69,075,872 TMF1
    nsv6554813inversion1nstd223human GRCh38 chr3: 69,032,628-69,033,274 , GRCh37.p13 chr3: 69,081,779-69,082,425 TMF1
    nsv6553901inversion1nstd223human GRCh38 chr3: 68,829,480-69,348,705 , GRCh37.p13 chr3: 68,878,631-69,397,856 TMF1, UBA3, 7 more genes
    nsv6545128inversion1nstd223human GRCh38 chr3: 69,026,620-69,027,017 , GRCh37.p13 chr3: 69,075,771-69,076,168 TMF1
    nsv6539829inversion1nstd223human GRCh38 chr3: 69,040,904-69,042,096 , GRCh37.p13 chr3: 69,090,055-69,091,247 TMF1
    nsv6370320copy number variation1nstd223human GRCh38 chr3: 68,567,314-69,424,179 , GRCh37.p13 chr3: 68,616,465-69,473,330 UBA3, EOGT, 9 more genes
    nsv6356586copy number variation1nstd223human GRCh38 chr3: 68,976,231-69,042,996 , GRCh37.p13 chr3: 69,025,382-69,092,147 TMF1, EOGT
    nsv6290933copy number variation1nstd102humanPathogenic GRCh37 chr3: 59,332,508-70,686,155 , GRCh38.p12 chr3: 59,346,782-70,637,004 NDUFB4P1, UBA3, 110 more genes
    nsv6290797copy number variation1nstd102humanUncertain significance GRCh37 chr3: 68,968,872-70,829,637 , GRCh38.p12 chr3: 68,919,721-70,780,486 UBA3, RNPC3P1, 17 more genes
    nsv6254164mobile element insertion1nstd215human GRCh38 chr3: 69,017,916-69,017,916 , GRCh37.p13 chr3: 69,067,067-69,067,067 TMF1
    nsv6134705copy number variation1nstd213human GRCh37 chr3: 66,270,000-87,730,001 , GRCh38.p12 chr3: 66,219,846-87,680,851 , AKR1B1P2, 187 more genes
    nsv6134704copy number variation1nstd213human GRCh37 chr3: 66,270,000-70,660,001 , GRCh38.p12 chr3: 66,219,846-70,610,850 , MITF, 40 more genes
    nsv6067318insertion1nstd212human GRCh38 chr3: 69,034,554-69,034,554 , GRCh37.p13 chr3: 69,083,705-69,083,705 TMF1
    nsv5902904copy number variation1nstd209human GRCh38 chr3: 66,803,410-74,489,186 , GRCh37.p13 chr3: 66,853,834-74,538,337 , LOC105377160, 83 more genes
    nsv5564432copy number variation1nstd102humanPathogenic GRCh37 chr3: 68,939,251-72,700,418 , GRCh38.p12 chr3: 68,890,100-72,651,267 CCDC137P1, LOC105377160, 39 more genes
    nsv5451257copy number variation1nstd206human GRCh38 chr3: 69,022,591-69,023,723 , GRCh37.p13 chr3: 69,071,742-69,072,874 TMF1
    nsv5318785copy number variation1nstd204human GRCh38.p13 chr3: 69,041,845-69,096,063 , GRCh37.p13 chr3: 69,090,996-69,145,214 MIR3136, ARL6IP5, 2 more genes
    nsv5238081copy number variation1nstd204human GRCh38.p13 chr3: 69,041,938-69,074,084 , GRCh37.p13 chr3: 69,091,089-69,123,235 MIR3136, TMF1, 1 more genes
    nsv5229412copy number variation1nstd204human GRCh38.p13 chr3: 69,041,638-69,046,837 , GRCh37.p13 chr3: 69,090,789-69,095,988 TMF1
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