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Items: 1 to 20 of 126

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148136copy number variation1nstd102humanPathogenic GRCh37 chr14: 100,367,259-101,508,462 , GRCh38.p12 chr14: 99,900,922-101,042,125 SNORD113-5, SNORD114-27, 99 more genes
    nsv7069088inversion1nstd229human GRCh38 chr14: 100,265,003-100,327,843 , GRCh37.p13 chr14: 100,731,340-100,794,180 SLC25A29, MIR6764, 4 more genes
    nsv7067062inversion1nstd229human GRCh38 chr14: 100,314,076-100,326,622 , GRCh37.p13 chr14: 100,780,413-100,792,959 SLC25A47, RN7SL523P
    nsv6975129copy number variation1nstd229human GRCh38 chr14: 100,322,891-100,327,180 , GRCh37.p13 chr14: 100,789,228-100,793,517 SLC25A47
    nsv6968289copy number variation1nstd229human GRCh38 chr14: 100,319,747-100,322,668 , GRCh37.p13 chr14: 100,786,084-100,789,005 RN7SL523P, SLC25A47
    nsv6966034copy number variation1nstd229human GRCh38 chr14: 100,117,901-100,472,900 , GRCh37.p13 chr14: 100,584,238-100,939,237 SLC25A47, MIR345, 10 more genes
    nsv6964556copy number variation1nstd229human GRCh38 chr14: 100,278,056-100,446,082 , GRCh37.p13 chr14: 100,744,393-100,912,419 WDR25, WARS1, 7 more genes
    nsv6959969copy number variation1nstd229human GRCh38 chr14: 100,322,784-100,322,856 , GRCh37.p13 chr14: 100,789,121-100,789,193 SLC25A47
    nsv6637825copy number variation1nstd102humanPathogenic GRCh37 chr14: 84,537,502-107,285,437 , GRCh38.p12 chr14: 84,071,158-106,877,229 CHGA, SNORD114-26, 676 more genes
    nsv6496588copy number variation1nstd223human GRCh38 chr14: 100,317,074-100,328,202 , GRCh37.p13 chr14: 100,783,411-100,794,539 SLC25A47, RN7SL523P
    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
    nsv6291768copy number variation1nstd102humanPathogenic GRCh37 chr14: 95,871,795-102,457,523 , GRCh38.p12 chr14: 95,405,458-101,991,186 CCDC85C, MEG3, 206 more genes
    nsv6288218insertion1nstd214human GRCh38 chr14: 100,322,799-100,322,799 , GRCh37.p13 chr14: 100,789,136-100,789,136 SLC25A47
    nsv6287886insertion1nstd214human GRCh38 chr14: 100,322,808-100,322,808 , GRCh37.p13 chr14: 100,789,145-100,789,145 SLC25A47
    nsv6287608insertion1nstd214human GRCh38 chr14: 100,322,814-100,322,814 , GRCh37.p13 chr14: 100,789,151-100,789,151 SLC25A47
    nsv6132885copy number variation1nstd213human GRCh37 chr14: 99,590,000-101,630,001 , GRCh38.p12 chr14: 99,123,663-101,163,664 DLK1, MEG8, 135 more genes
    nsv6082257insertion1nstd212human GRCh38 chr14: 100,322,825-100,322,825 , GRCh37.p13 chr14: 100,789,162-100,789,162 SLC25A47
    nsv5941646copy number variation1nstd209human GRCh38 chr14: 100,322,784-100,322,855 , GRCh37.p13 chr14: 100,789,121-100,789,192 SLC25A47
    nsv5655302insertion1nstd207human GRCh38 chr14: 100,322,814-100,322,814 , GRCh37.p13 chr14: 100,789,151-100,789,151 SLC25A47
    nsv5511715copy number variation1nstd206human GRCh38 chr14: 100,322,784-100,322,857 , GRCh37.p13 chr14: 100,789,121-100,789,194 SLC25A47
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