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Items: 1 to 20 of 977

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5957586insertion1nstd209human GRCh38 chr4: 175,769,518-175,769,518 , GRCh37.p13 chr4: 176,690,669-176,690,669 GPM6A
    nsv5905463copy number variation1nstd209human GRCh38 chr4: 175,786,710-175,788,083 , GRCh37.p13 chr4: 176,707,861-176,709,234 GPM6A
    nsv5903807copy number variation1nstd209human GRCh38 chr4: 175,944,910-175,945,044 , GRCh37.p13 chr4: 176,866,061-176,866,195 GPM6A, LOC107984113
    nsv5903667copy number variation1nstd209human GRCh38 chr4: 175,750,464-175,758,814 , GRCh37.p13 chr4: 176,671,615-176,679,965 GPM6A
    nsv5903483copy number variation1nstd209human GRCh38 chr4: 175,770,250-175,770,370 , GRCh37.p13 chr4: 176,691,401-176,691,521 GPM6A
    nsv5898944copy number variation1nstd209human GRCh38 chr4: 175,995,877-175,995,994 , GRCh37.p13 chr4: 176,917,028-176,917,145 GPM6A
    nsv5892823copy number variation1nstd209human GRCh38 chr4: 175,978,330-175,987,773 , GRCh37.p13 chr4: 176,899,481-176,908,924 GPM6A
    nsv5890627copy number variation1nstd209human GRCh38 chr4: 175,710,761-175,711,458 , GRCh37.p13 chr4: 176,631,912-176,632,609 GPM6A
    nsv5838705copy number variation1nstd209human GRCh38 chr4: 175,786,680-175,788,099 , GRCh37.p13 chr4: 176,707,831-176,709,250 GPM6A
    nsv5838444copy number variation2nstd209human GRCh38 chr4: 175,978,962-175,979,962 , GRCh37.p13 chr4: 176,900,113-176,901,113 GPM6A
    nsv5838153copy number variation1nstd209human GRCh38 chr4: 175,978,262-175,987,429 , GRCh37.p13 chr4: 176,899,413-176,908,580 GPM6A
    nsv5838152copy number variation1nstd209human GRCh38 chr4: 175,750,419-175,758,863 , GRCh37.p13 chr4: 176,671,570-176,680,014 GPM6A
    nsv5720619mobile element insertion1nstd211human GRCh38 chr4: 175,727,863-175,727,863 , GRCh37.p13 chr4: 176,649,014-176,649,014 GPM6A
    nsv5685352mobile element insertion1nstd211human GRCh38 chr4: 175,634,611-175,634,611 , GRCh37.p13 chr4: 176,555,762-176,555,762 GPM6A
    nsv5681856mobile element insertion1nstd211human GRCh38 chr4: 175,937,264-175,937,264 , GRCh37.p13 chr4: 176,858,415-176,858,415 LOC107984113, GPM6A
    nsv5679013mobile element insertion2nstd211human GRCh38 chr4: 175,956,722-175,956,722 , GRCh37.p13 chr4: 176,877,873-176,877,873 LOC107984113, GPM6A
    nsv5576744copy number variation1nstd207human GRCh38 chr4: 175,995,877-175,995,994 , GRCh37.p13 chr4: 176,917,028-176,917,145 GPM6A
    nsv5565992copy number variation1nstd207human GRCh38 chr4: 175,637,650-175,637,748 , GRCh37.p13 chr4: 176,558,801-176,558,899 GPM6A
    nsv5562145sequence alteration1nstd206human GRCh38 chr4: 74,717,205-184,730,527 , GRCh37.p13 chr4: 75,689,880-185,651,681 , ASS1P8, 1307 more genes
    nsv5536761insertion1nstd206human GRCh38 chr4: 175,956,722-175,956,766 , GRCh37.p13 chr4: 176,877,873-176,877,917 GPM6A, LOC107984113
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