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Items: 1 to 20 of 196

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6131383insertion1nstd186human GRCh37 chr12: 73,580,549-73,580,549 , GRCh38.p12 chr12: 73,186,769-73,186,769 LINC02444
    nsv6112755copy number variation1nstd102humanPathogenic GRCh37 chr12: 65,251,705-75,263,379 , GRCh38.p12 chr12: 64,857,925-74,869,599 LINC02421, TBC1D15, 144 more genes
    nsv5658289insertion1nstd207human GRCh38 chr12: 73,186,764-73,186,764 , GRCh37.p13 chr12: 73,580,544-73,580,544 LINC02444
    nsv5536535insertion1nstd206human GRCh38 chr12: 73,186,769-73,186,769 , GRCh37.p13 chr12: 73,580,549-73,580,549 LINC02444
    nsv5365113translocation1nstd200human GRCh38 chr12: 73,177,977-73,177,977 , GRCh38 chr12: 73,179,179-73,179,179 , GRCh37.p13 chr12: 73,572,959-73,572,959 , GRCh37.p13 chr12: 73,571,757-73,571,757 LINC02444
    nsv5365112translocation1nstd200human GRCh38 chr12: 73,177,864-73,177,864 , GRCh38 chr12: 73,179,187-73,179,187 , GRCh37.p13 chr12: 73,571,644-73,571,644 , GRCh37.p13 chr12: 73,572,967-73,572,967 LINC02444
    nsv5356084translocation1nstd200human GRCh38 chr12: 73,158,835-73,158,835 , GRCh38 chr12: 73,159,021-73,159,021 , GRCh37.p13 chr12: 73,552,615-73,552,615 , GRCh37.p13 chr12: 73,552,801-73,552,801 LINC02444
    nsv5330714translocation1nstd200human GRCh37 chr12: 73,572,967-73,572,967 , GRCh37 chr12: 73,571,644-73,571,644 , GRCh38.p12 chr12: 73,177,864-73,177,864 , GRCh38.p12 chr12: 73,179,187-73,179,187 LINC02444
    nsv5329858translocation1nstd200human GRCh37 chr12: 73,571,757-73,571,757 , GRCh37 chr12: 73,572,959-73,572,959 , GRCh38.p12 chr12: 73,179,179-73,179,179 , GRCh38.p12 chr12: 73,177,977-73,177,977 LINC02444
    nsv5266526copy number variation1nstd204human GRCh38.p13 chr12: 73,150,825-73,184,509 , GRCh37.p13 chr12: 73,544,605-73,578,289 LINC02444
    nsv5263778copy number variation1nstd204human GRCh38.p13 chr12: 73,150,501-73,287,700 , GRCh37.p13 chr12: 73,544,281-73,681,480 LINC02444
    nsv5121085mobile element insertion1nstd203human GRCh38 chr12: 73,186,946-73,186,946 , GRCh37.p13 chr12: 73,580,726-73,580,726 LINC02444
    nsv5037136inversion1nstd200human GRCh38 chr12: 69,787,024-109,882,221 , GRCh37.p13 chr12: 70,180,804-110,320,026 , RPL23AP68, 540 more genes
    nsv5036282inversion1nstd200human GRCh38 chr12: 52,338,357-95,425,642 , GRCh37.p13 chr12: 52,732,141-95,819,418 , MIR6502, 769 more genes
    nsv5032581inversion1nstd200human GRCh38 chr12: 67,763,754-90,678,993 , GRCh37.p13 chr12: 68,157,534-91,072,770 , LOC105369886, 255 more genes
    nsv5006005copy number variation1nstd200human GRCh38 chr12: 73,087,769-73,223,130 , GRCh37.p13 chr12: 73,481,549-73,616,910 LINC02444
    nsv4888823inversion1nstd200human GRCh37 chr12: 68,157,543-91,072,771 , GRCh38.p12 chr12: 67,763,763-90,678,994 , BEST3, 255 more genes
    nsv4886161inversion1nstd200human GRCh37 chr12: 70,180,810-110,320,027 , GRCh38.p12 chr12: 69,787,030-109,882,222 , LOC728739, 540 more genes
    nsv4883504inversion1nstd200human GRCh37 chr12: 52,732,141-95,819,418 , GRCh38.p12 chr12: 52,338,357-95,425,642 , MYL6B, 769 more genes
    nsv4845948copy number variation1nstd200human GRCh37 chr12: 73,481,549-73,616,910 , GRCh38.p12 chr12: 73,087,769-73,223,130 LINC02444
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