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Items: 1 to 20 of 881

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7145702copy number variation1nstd232human GRCh37.p13 chr3: 47,891,042-47,891,116 , GRCh38.p12 chr3: 47,849,552-47,849,626 MAP4, DHX30, 1 more genes
    nsv7142726copy number variation1nstd232human GRCh37.p13 chr3: 47,890,305-47,890,406 , GRCh38.p12 chr3: 47,848,815-47,848,916 MAP4, DHX30, 1 more genes
    nsv7096956copy number variation1nstd102humanUncertain significance GRCh37 chr3: 47,422,587-47,919,033 , GRCh38.p12 chr3: 47,381,097-47,877,543 BOLA2P2, RN7SL870P, 12 more genes
    nsv7096805copy number variation1nstd102humanUncertain significance GRCh37 chr3: 45,435,946-49,137,751 , GRCh38.p12 chr3: 45,394,454-49,100,318 SNORA94, LIMD1-AS1, 120 more genes
    nsv7057834inversion1nstd229human GRCh38 chr3: 47,958,164-47,958,264 , GRCh37.p13 chr3: 47,999,654-47,999,754 MAP4
    nsv7047381inversion1nstd229human GRCh38 chr3: 47,589,597-48,210,528 , GRCh37.p13 chr3: 47,631,087-48,252,018 CDC25A, SNORD146, 12 more genes
    nsv7043643inversion1nstd229human GRCh38 chr3: 47,927,890-47,927,985 , GRCh37.p13 chr3: 47,969,380-47,969,475 MAP4
    nsv6717954copy number variation1nstd229human GRCh38 chr3: 47,896,028-48,196,668 , GRCh37.p13 chr3: 47,937,518-48,238,158 MAP4, RN7SL664P, 7 more genes
    nsv6717877copy number variation1nstd229human GRCh38 chr3: 47,899,559-47,899,731 , GRCh37.p13 chr3: 47,941,049-47,941,221 MAP4
    nsv6717241copy number variation1nstd229human GRCh38 chr3: 47,885,889-47,995,023 , GRCh37.p13 chr3: 47,927,379-48,036,513 MAP4, VPS26BP1
    nsv6716424copy number variation1nstd229human GRCh38 chr3: 47,980,590-47,984,005 , GRCh37.p13 chr3: 48,022,080-48,025,495 MAP4
    nsv6715659copy number variation1nstd229human GRCh38 chr3: 48,078,640-48,084,130 , GRCh37.p13 chr3: 48,120,130-48,125,620 MAP4
    nsv6715658copy number variation1nstd229human GRCh38 chr3: 48,024,053-48,027,586 , GRCh37.p13 chr3: 48,065,543-48,069,076 MAP4
    nsv6714658copy number variation1nstd229human GRCh38 chr3: 48,015,504-48,015,654 , GRCh37.p13 chr3: 48,056,994-48,057,144 MAP4
    nsv6714299copy number variation1nstd229human GRCh38 chr3: 47,987,266-47,995,365 , GRCh37.p13 chr3: 48,028,756-48,036,855 MAP4
    nsv6713719copy number variation1nstd229human GRCh38 chr3: 48,013,497-48,016,100 , GRCh37.p13 chr3: 48,054,987-48,057,590 MAP4
    nsv6713055copy number variation1nstd229human GRCh38 chr3: 47,904,024-47,914,783 , GRCh37.p13 chr3: 47,945,514-47,956,273 MAP4
    nsv6713047copy number variation1nstd229human GRCh38 chr3: 47,942,266-47,948,605 , GRCh37.p13 chr3: 47,983,756-47,990,095 MAP4
    nsv6712437copy number variation1nstd229human GRCh38 chr3: 47,953,491-47,959,946 , GRCh37.p13 chr3: 47,994,981-48,001,436 VPS26BP1, MAP4
    nsv6711282copy number variation1nstd229human GRCh38 chr3: 47,883,704-47,885,852 , GRCh37.p13 chr3: 47,925,194-47,927,342 MAP4
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