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Items: 1 to 20 of 191

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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
    nsv7095836copy number variation3nstd102humanUncertain significance, Pathogenic GRCh37 chr22: 37,154,355-39,148,633 , GRCh38.p12 chr22: 36,758,311-38,752,628 CSF2RBP1, H1-0, 80 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
    nsv7072766inversion1nstd229human GRCh38 chr22: 35,603,617-39,341,195 , GRCh37.p13 chr22: 35,999,664-39,737,200 APOL5, MTATP6P20, 132 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
    nsv7061959inversion1nstd229human GRCh38 chr22: 36,818,005-44,993,640 , GRCh37.p13 chr22: 37,214,049-45,389,520 SMIM45, A4GALT, 271 more genes
    nsv7061838inversion1nstd229human GRCh38 chr22: 37,240,163-37,373,633 , GRCh37.p13 chr22: 37,636,203-37,769,673 RAC2, CYTH4, 4 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
    nsv7031662copy number variation1nstd229human GRCh38 chr22: 37,226,041-37,231,230 , GRCh37.p13 chr22: 37,622,081-37,627,270 RAC2
    nsv7030848copy number variation1nstd229human GRCh38 chr22: 37,230,604-37,231,278 , GRCh37.p13 chr22: 37,626,644-37,627,318 RAC2
    nsv7026588copy number variation1nstd229human GRCh38 chr22: 36,570,594-37,316,473 , GRCh37.p13 chr22: 36,966,641-37,712,514 LL22NC01-81G9.3, IFT27, 24 more genes
    nsv7023843copy number variation1nstd229human GRCh38 chr22: 37,226,804-37,231,230 , GRCh37.p13 chr22: 37,622,844-37,627,270 RAC2
    nsv7018763copy number variation1nstd229human GRCh38 chr22: 37,226,028-37,226,707 , GRCh37.p13 chr22: 37,622,068-37,622,747 RAC2
    nsv6311132copy number variation1nstd102humanUncertain significance GRCh37 chr22: 37,622,713-37,640,188 , GRCh38.p12 chr22: 37,226,673-37,244,148 RAC2
    nsv6307543copy number variation1nstd186human GRCh37 chr22: 37,622,935-37,623,561 , GRCh38.p12 chr22: 37,226,895-37,227,521 RAC2
    nsv6306349copy number variation1nstd186human GRCh37 chr22: 37,623,034-37,623,707 , GRCh38.p12 chr22: 37,226,994-37,227,667 RAC2
    nsv6147002copy number variation1nstd206human GRCh38 chr22: 37,226,994-37,227,667 , GRCh37.p13 chr22: 37,623,034-37,623,707 RAC2
    nsv6146335copy number variation1nstd206human GRCh38 chr22: 37,226,895-37,227,521 , GRCh37.p13 chr22: 37,622,935-37,623,561 RAC2
    nsv6134213copy number variation1nstd213human GRCh37 chr22: 37,470,000-39,980,001 , GRCh38.p12 chr22: 37,073,960-39,583,996 ATF4, COX5BP7, 98 more genes
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