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Items: 1 to 20 of 586

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    nsv7095835copy number variation1nstd102humanUncertain significance GRCh37 chr22: 36,152,132-36,156,099 , GRCh38.p12 chr22: 35,756,085-35,760,052 , GRCh38.p12 chr22|NT_187630.1: 77,083-81,050 RBFOX2
    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
    nsv7072766inversion1nstd229human GRCh38 chr22: 35,603,617-39,341,195 , GRCh37.p13 chr22: 35,999,664-39,737,200 APOL5, MTATP6P20, 132 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
    nsv7071545inversion1nstd229human GRCh38 chr22: 35,827,031-35,827,133 , GRCh37.p13 chr22: 36,223,078-36,223,180 RBFOX2
    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
    nsv7059210inversion1nstd229human GRCh38 chr22: 35,603,611-39,337,136 , GRCh37.p13 chr22: 35,999,658-39,733,141 MTCO2P20, RPS29P31, 132 more genes
    nsv7058312inversion1nstd229human GRCh38 chr22: 35,869,510-35,873,173 , GRCh37.p13 chr22: 36,265,557-36,269,220 RBFOX2
    nsv7036775copy number variation1nstd229human GRCh38 chr22: 35,943,863-35,961,683 , GRCh37.p13 chr22: 36,339,911-36,357,731 RBFOX2
    nsv7035126copy number variation1nstd229human GRCh38 chr22: 35,929,658-35,961,385 , GRCh37.p13 chr22: 36,325,706-36,357,433 RBFOX2
    nsv7034794copy number variation1nstd229human GRCh38 chr22: 35,984,930-36,136,063 , GRCh37.p13 chr22: 36,380,978-36,532,111 RBFOX2
    nsv7033809copy number variation1nstd229human GRCh38 chr22: 35,737,477-35,738,198 , GRCh37.p13 chr22: 36,133,524-36,134,245 RBFOX2
    nsv7031297copy number variation1nstd229human GRCh38 chr22: 36,000,549-36,005,302 , GRCh37.p13 chr22: 36,396,597-36,401,350 RBFOX2
    nsv7031255copy number variation1nstd229human GRCh38 chr22: 35,884,447-35,889,179 , GRCh37.p13 chr22: 36,280,494-36,285,226 RBFOX2
    nsv7030621copy number variation1nstd229human GRCh38 chr22: 35,730,802-35,738,125 , GRCh37.p13 chr22: 36,126,849-36,134,172 RBFOX2, APOL5
    nsv7030514copy number variation1nstd229human GRCh38 chr22: 35,882,852-35,888,972 , GRCh37.p13 chr22: 36,278,899-36,285,019 RBFOX2
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