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Items: 1 to 20 of 144

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7093363copy number variation1nstd102humanPathogenic GRCh37 chr6: 820,000-21,700,000 , GRCh38.p12 chr6: 820,000-21,699,769 LOC101928354, CNN3P1, 321 more genes
    nsv7058053inversion1nstd229human GRCh38 chr6: 12,061,960-18,307,388 , GRCh37.p13 chr6: 12,062,193-18,307,619 RNU7-133P, CAP2, 87 more genes
    nsv7039975inversion1nstd229human GRCh38 chr6: 17,283,249-17,283,338 , GRCh37.p13 chr6: 17,283,480-17,283,569 RBM24
    nsv6797302copy number variation1nstd229human GRCh38 chr6: 17,280,901-17,281,900 , GRCh37.p13 chr6: 17,281,132-17,282,131 RBM24
    nsv6796454copy number variation1nstd229human GRCh38 chr6: 17,245,162-17,281,997 , GRCh37.p13 chr6: 17,245,393-17,282,228 RBM24
    nsv6791368copy number variation1nstd229human GRCh38 chr6: 17,286,601-17,290,800 , GRCh37.p13 chr6: 17,286,832-17,291,031 RBM24
    nsv6790565copy number variation1nstd229human GRCh38 chr6: 16,741,614-19,141,206 , GRCh37.p13 chr6: 16,741,845-19,141,437 LOC105374951, RNU6-263P, 34 more genes
    nsv6784750copy number variation1nstd229human GRCh38 chr6: 16,883,993-17,512,482 , GRCh37.p13 chr6: 16,884,224-17,512,713 LOC101928463, CAP2, 6 more genes
    nsv6636333copy number variation1nstd102humanPathogenic GRCh37 chr6: 12,005,630-22,849,647 , GRCh38.p12 chr6: 12,005,397-22,849,418 SOX4, MDH1P2, 136 more genes
    nsv6560312inversion1nstd223human GRCh38 chr6: 17,294,265-17,295,051 , GRCh37.p13 chr6: 17,294,496-17,295,282 RBM24
    nsv6135469copy number variation1nstd213human GRCh37 chr6: 11,730,000-19,840,001 , GRCh38.p12 chr6: 11,729,767-19,839,770 EDN1, GMPR, 115 more genes
    nsv6005399copy number variation1nstd212human GRCh38 chr6: 17,290,545-17,357,076 , GRCh37.p13 chr6: 17,290,776-17,357,307 RBM24
    nsv5898619copy number variation1nstd209human GRCh38 chr6: 17,287,321-17,289,164 , GRCh37.p13 chr6: 17,287,552-17,289,395 RBM24
    nsv5844543copy number variation1nstd209human GRCh38 chr6: 17,287,266-17,289,165 , GRCh37.p13 chr6: 17,287,497-17,289,396 RBM24
    nsv5032127inversion1nstd200human GRCh38 chr6: 17,263,273-17,371,253 , GRCh37.p13 chr6: 17,263,504-17,371,484 RBM24
    nsv4934458copy number variation1nstd200human GRCh38 chr6: 17,245,162-17,282,001 , GRCh37.p13 chr6: 17,245,393-17,282,232 RBM24
    nsv4882483inversion1nstd200human GRCh37 chr6: 17,263,504-17,371,484 , GRCh38.p12 chr6: 17,263,273-17,371,253 RBM24
    nsv4828517copy number variation1nstd200human GRCh37 chr6: 17,245,393-17,282,232 , GRCh38.p12 chr6: 17,245,162-17,282,001 RBM24
    nsv4496561mobile element insertion1nstd166human GRCh37.p13 chr6: 17,282,934-17,282,934 , GRCh38.p12 chr6: 17,282,703-17,282,703 RBM24
    nsv4456780copy number variation1nstd102humanPathogenic GRCh37 chr6: 156,974-23,221,621 , GRCh38.p12 chr6: 156,974-23,221,393 LOC105374960, LOC101928573, 342 more genes
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