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Items: 1 to 20 of 263

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7146763copy number variation1nstd232human GRCh37.p13 chr22: 35,799,325-35,799,404 , GRCh38.p12 chr22: 35,403,332-35,403,411 MCM5
    nsv7145949insertion1nstd232human GRCh37.p13 chr22: 35,845,573-35,845,573 , GRCh38.p12 chr22: 35,449,580-35,449,580 MCM5
    nsv7140262insertion1nstd232human GRCh37.p13 chr22: 35,812,807-35,812,807 , GRCh38.p12 chr22: 35,416,814-35,416,814 MCM5
    nsv7096308copy number variation1nstd102humanUncertain significance GRCh37 chr22: 35,776,672-42,486,826 , GRCh38.p12 chr22: 35,380,679-42,090,822 CDC42EP1, SREBF2, 231 more genes
    nsv7078067inversion1nstd229human GRCh38 chr22: 30,287,061-38,012,264 , GRCh37.p13 chr22: 30,683,050-38,408,271 LINC02885, RN7SL20P, 203 more genes
    nsv7073169inversion1nstd229human GRCh38 chr22: 33,518,915-36,078,559 , GRCh37.p13 chr22: 33,914,901-36,474,607 ISX, MRPS16P3, 33 more genes
    nsv7072941inversion1nstd229human GRCh38 chr22: 33,518,918-36,085,749 , GRCh37.p13 chr22: 33,914,904-36,481,797 ISX, LOC105373014, 33 more genes
    nsv7072171inversion1nstd229human GRCh38 chr22: 34,919,966-36,817,658 , GRCh37.p13 chr22: 35,315,956-37,213,702 APOL4, RBFOX2, 45 more genes
    nsv7065500inversion1nstd229human GRCh38 chr22: 29,260,563-37,652,385 , GRCh37.p13 chr22: 29,656,552-38,048,392 RFPL1, PATZ1, 217 more genes
    nsv7064066inversion1nstd229human GRCh38 chr22: 34,920,312-39,418,308 , GRCh37.p13 chr22: 35,316,302-39,814,313 LOC112268295, APOBEC3B-AS1, 150 more genes
    nsv7031531copy number variation1nstd229human GRCh38 chr22: 35,431,367-35,635,060 , GRCh37.p13 chr22: 35,827,360-36,031,107 MCM5, LOC284912, 4 more genes
    nsv7029772copy number variation1nstd229human GRCh38 chr22: 35,437,115-35,472,545 , GRCh37.p13 chr22: 35,833,108-35,868,538 MCM5
    nsv7028988copy number variation1nstd229human GRCh38 chr22: 35,406,574-35,406,785 , GRCh37.p13 chr22: 35,802,567-35,802,778 MCM5
    nsv7026865copy number variation1nstd229human GRCh38 chr22: 35,424,613-35,440,261 , GRCh37.p13 chr22: 35,820,606-35,836,254 MCM5
    nsv7026752copy number variation1nstd229human GRCh38 chr22: 35,442,382-35,447,030 , GRCh37.p13 chr22: 35,838,375-35,843,023 MCM5
    nsv7026587copy number variation1nstd229human GRCh38 chr22: 35,448,374-35,448,402 , GRCh37.p13 chr22: 35,844,367-35,844,395 MCM5
    nsv7025825copy number variation1nstd229human GRCh38 chr22: 35,417,460-35,417,489 , GRCh37.p13 chr22: 35,813,453-35,813,482 MCM5
    nsv7024298copy number variation1nstd229human GRCh38 chr22: 35,395,704-35,398,208 , GRCh37.p13 chr22: 35,791,697-35,794,201 MCM5
    nsv7022776copy number variation1nstd229human GRCh38 chr22: 35,449,611-35,467,009 , GRCh37.p13 chr22: 35,845,604-35,863,002 MCM5
    nsv7021791copy number variation1nstd229human GRCh38 chr22: 35,441,892-35,461,869 , GRCh37.p13 chr22: 35,837,885-35,857,862 MCM5
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