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Items: 1 to 20 of 302

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5964294insertion1nstd209human GRCh38 chr9: 76,442,853-76,442,853 , GRCh37.p13 chr9: 79,057,769-79,057,769 GCNT1
    nsv5927031copy number variation1nstd209human GRCh38 chr9: 76,446,883-76,454,108 , GRCh37.p13 chr9: 79,061,799-79,069,024 GCNT1
    nsv5924630copy number variation1nstd209human GRCh38 chr9: 76,506,341-76,509,728 , GRCh37.p13 chr9: 79,121,257-79,124,644 GCNT1
    nsv5919601copy number variation1nstd209human GRCh38 chr9: 76,443,894-76,443,989 , GRCh37.p13 chr9: 79,058,810-79,058,905 GCNT1
    nsv5918369copy number variation1nstd209human GRCh38 chr9: 76,467,302-76,468,156 , GRCh37.p13 chr9: 79,082,218-79,083,072 GCNT1
    nsv5908603copy number variation1nstd209human GRCh38 chr9: 76,445,572-76,445,644 , GRCh37.p13 chr9: 79,060,488-79,060,560 GCNT1
    nsv5865256copy number variation1nstd209human GRCh38 chr9: 76,449,095-76,452,094 , GRCh37.p13 chr9: 79,064,011-79,067,010 GCNT1
    nsv5865195copy number variation1nstd209human GRCh38 chr9: 76,446,895-76,453,894 , GRCh37.p13 chr9: 79,061,811-79,068,810 GCNT1
    nsv5856874copy number variation1nstd209human GRCh38 chr9: 76,447,795-76,449,594 , GRCh37.p13 chr9: 79,062,711-79,064,510 GCNT1
    nsv5854205copy number variation1nstd209human GRCh38 chr9: 76,506,258-76,509,557 , GRCh37.p13 chr9: 79,121,174-79,124,473 GCNT1
    nsv5708938mobile element insertion2nstd211human GRCh38 chr9: 76,442,868-76,442,868 , GRCh37.p13 chr9: 79,057,784-79,057,784 GCNT1
    nsv5640799insertion1nstd207human GRCh38 chr9: 76,442,853-76,442,853 , GRCh37.p13 chr9: 79,057,769-79,057,769 GCNT1
    nsv5598854copy number variation1nstd207human GRCh38 chr9: 76,443,894-76,443,989 , GRCh37.p13 chr9: 79,058,810-79,058,905 GCNT1
    nsv5585129copy number variation1nstd207human GRCh38 chr9: 76,445,572-76,445,644 , GRCh37.p13 chr9: 79,060,488-79,060,560 GCNT1
    nsv5493594copy number variation1nstd206human GRCh38 chr9: 76,499,230-76,499,285 , GRCh37.p13 chr9: 79,114,146-79,114,201 GCNT1
    nsv5483885copy number variation1nstd206human GRCh38 chr9: 76,474,256-76,474,354 , GRCh37.p13 chr9: 79,089,172-79,089,270 GCNT1
    nsv5481560copy number variation1nstd206human GRCh38 chr9: 76,445,573-76,445,645 , GRCh37.p13 chr9: 79,060,489-79,060,561 GCNT1
    nsv5480305copy number variation1nstd206human GRCh38 chr9: 76,451,420-76,451,473 , GRCh37.p13 chr9: 79,066,336-79,066,389 GCNT1
    nsv5475295copy number variation1nstd206human GRCh38 chr9: 76,443,900-76,443,990 , GRCh37.p13 chr9: 79,058,816-79,058,906 GCNT1
    nsv5409682mobile element insertion1nstd206human GRCh38 chr9: 76,442,868-76,442,919 , GRCh37.p13 chr9: 79,057,784-79,057,835 GCNT1
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