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Items: 1 to 20 of 125

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7060054inversion1nstd229human GRCh38 chr14: 77,012,562-77,945,687 , GRCh37.p13 chr14: 77,478,905-78,412,030 GSTZ1, FAM204DP, 28 more genes
    nsv6973838copy number variation1nstd229human GRCh38 chr14: 76,851,033-77,188,336 , GRCh37.p13 chr14: 77,317,376-77,654,679 LINC01629, FAM204DP, 13 more genes
    nsv6967063copy number variation1nstd229human GRCh38 chr14: 77,135,576-77,138,048 , GRCh37.p13 chr14: 77,601,919-77,604,391 ZDHHC22
    nsv6959895copy number variation1nstd229human GRCh38 chr14: 76,053,610-84,350,797 , GRCh37.p13 chr14: 76,519,953-84,817,141 LINC02308, LOC105370573, 102 more genes
    nsv6959609copy number variation1nstd229human GRCh38 chr14: 77,141,412-77,507,959 , GRCh37.p13 chr14: 77,607,755-77,974,302 SPTLC2, NOXRED1, 13 more genes
    nsv6958675copy number variation1nstd229human GRCh38 chr14: 76,689,901-77,420,500 , GRCh37.p13 chr14: 77,156,244-77,886,843 ANGEL1, RN7SKP17, 26 more genes
    nsv6958630copy number variation1nstd229human GRCh38 chr14: 77,144,407-77,148,070 , GRCh37.p13 chr14: 77,610,750-77,614,413 ZDHHC22
    nsv6577345inversion1nstd223human GRCh38 chr14: 77,012,562-77,945,687 , GRCh37.p13 chr14: 77,478,905-78,412,030 NOXRED1, FAM204DP, 28 more genes
    nsv6476297copy number variation1nstd223human GRCh38 chr14: 77,144,406-77,148,068 , GRCh37.p13 chr14: 77,610,749-77,614,411 ZDHHC22
    nsv6315524copy number variation1nstd102humanPathogenic GRCh37 chr14: 37,671,058-106,985,955 , GRCh38.p12 chr14: 37,201,853-106,530,013 PAPOLA-DT, LOC105378180, 1338 more genes
    nsv6132793copy number variation1nstd213human GRCh37 chr14: 77,080,000-88,760,001 , GRCh38.p12 chr14: 76,613,657-88,293,657 GALC, GSTZ1, 120 more genes
    nsv5931678copy number variation1nstd209human GRCh38 chr14: 75,925,125-77,416,814 , GRCh37.p13 chr14: 76,391,468-77,883,157 TMED8, LOC105370573, 37 more genes
    nsv5511825copy number variation1nstd206human GRCh38 chr14: 77,144,407-77,148,068 , GRCh37.p13 chr14: 77,610,750-77,614,411 ZDHHC22
    nsv5499310copy number variation1nstd206human GRCh38 chr14: 77,135,576-77,138,044 , GRCh37.p13 chr14: 77,601,919-77,604,387 ZDHHC22
    nsv5032025inversion1nstd200human GRCh38 chr14: 53,190,097-88,878,877 , GRCh37.p13 chr14: 53,656,815-89,345,221 , IFT43, 578 more genes
    nsv5000168copy number variation1nstd200human GRCh38 chr14: 77,144,407-77,148,068 , GRCh37.p13 chr14: 77,610,750-77,614,411 ZDHHC22
    nsv4622487copy number variation1nstd183human GRCh37 chr14: 77,610,723-77,614,385 , GRCh38.p12 chr14: 77,144,380-77,148,042 ZDHHC22
    nsv4456664copy number variation1nstd102humanPathogenic GRCh37 chr14: 77,274,990-89,803,137 , GRCh38.p12 chr14: 76,808,647-89,336,793 DYNLL1P2, GTF2A1, 126 more genes
    nsv4456648copy number variation1nstd102humanUncertain significance GRCh37 chr14: 77,587,406-77,698,358 , GRCh38.p12 chr14: 77,121,063-77,232,015 ZDHHC22, TMEM63C, 1 more genes
    nsv4376851copy number variation1nstd173human GRCh37 chr14: 77,042,465-77,865,966 , GRCh38.p12 chr14: 76,576,122-77,399,623 NGB, VASH1, 29 more genes
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