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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7099206copy number variation1nstd231human GRCh38.p12 chr1: 54,693,460-58,571,894 , GRCh37 chr1: 55,159,133-59,037,566 C8A, C8B, 49 more genes
    nsv7054245inversion1nstd229human GRCh38 chr1: 56,961,702-56,971,609 , GRCh37.p13 chr1: 57,427,375-57,437,282 C8B
    nsv7043988inversion1nstd229human GRCh38 chr1: 56,959,965-56,960,060 , GRCh37.p13 chr1: 57,425,638-57,425,733 C8B
    nsv6652270copy number variation1nstd229human GRCh38 chr1: 56,963,968-56,966,163 , GRCh37.p13 chr1: 57,429,641-57,431,836 C8B
    nsv6652269copy number variation1nstd229human GRCh38 chr1: 56,947,890-56,951,791 , GRCh37.p13 chr1: 57,413,563-57,417,464 C8B
    nsv6652268copy number variation1nstd229human GRCh38 chr1: 56,938,352-56,951,167 , GRCh37.p13 chr1: 57,404,025-57,416,840 C8B
    nsv6652172copy number variation1nstd229human GRCh38 chr1: 56,942,969-56,951,532 , GRCh37.p13 chr1: 57,408,642-57,417,205 C8B
    nsv6652171copy number variation1nstd229human GRCh38 chr1: 56,933,538-56,933,945 , GRCh37.p13 chr1: 57,399,211-57,399,618 C8B
    nsv6651504copy number variation1nstd229human GRCh38 chr1: 56,959,066-56,965,742 , GRCh37.p13 chr1: 57,424,739-57,431,415 C8B
    nsv6651503copy number variation1nstd229human GRCh38 chr1: 56,916,360-56,929,754 , GRCh37.p13 chr1: 57,382,033-57,395,427 C8A, C8B
    nsv6651496copy number variation1nstd229human GRCh38 chr1: 56,712,664-57,189,564 , GRCh37.p13 chr1: 57,178,337-57,655,237 LOC112267900, DAB1, 6 more genes
    nsv6637046copy number variation1nstd102humanUncertain significance GRCh37 chr1: 57,137,390-59,037,566 , GRCh38.p12 chr1: 56,671,717-58,571,894 OMA1, C8A, 15 more genes
    nsv6326482copy number variation1nstd223human GRCh38 chr1: 56,938,352-56,951,166 , GRCh37.p13 chr1: 57,404,025-57,416,839 C8B
    nsv6323019copy number variation1nstd223human GRCh38 chr1: 56,947,890-56,951,788 , GRCh37.p13 chr1: 57,413,563-57,417,461 C8B
    nsv6319975copy number variation1nstd223human GRCh38 chr1: 56,967,298-57,018,977 , GRCh37.p13 chr1: 57,432,971-57,484,650 C8B, LOC112267900, 2 more genes
    nsv6318094copy number variation1nstd223human GRCh38 chr1: 56,951,163-56,952,768 , GRCh37.p13 chr1: 57,416,836-57,418,441 C8B
    nsv6310970copy number variation1nstd102humanUncertain significance GRCh37 chr1: 57,415,208-57,415,445 , GRCh38.p12 chr1: 56,949,535-56,949,772 C8B
    nsv6133874copy number variation1nstd213human GRCh37 chr1: 56,220,000-57,410,001 , GRCh38.p12 chr1: 55,754,327-56,944,328 C8A, C8B, 14 more genes
    nsv6057145insertion1nstd212human GRCh38 chr1: 56,929,081-56,929,081 , GRCh37.p13 chr1: 57,394,754-57,394,754 C8B
    nsv5963130insertion1nstd209human GRCh38 chr1: 56,929,084-56,929,084 , GRCh37.p13 chr1: 57,394,757-57,394,757 C8B
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