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Items: 1 to 20 of 133

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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
    nsv7059210inversion1nstd229human GRCh38 chr22: 35,603,611-39,337,136 , GRCh37.p13 chr22: 35,999,658-39,733,141 MTCO2P20, RPS29P31, 132 more genes
    nsv7028509copy number variation1nstd229human GRCh38 chr22: 37,019,286-37,024,655 , GRCh37.p13 chr22: 37,415,327-37,420,696 MPST, TST
    nsv7027530copy number variation1nstd229human GRCh38 chr22: 37,016,109-37,028,634 , GRCh37.p13 chr22: 37,412,150-37,424,675 MPST, TST
    nsv7026754copy number variation1nstd229human GRCh38 chr22: 37,027,045-37,029,571 , GRCh37.p13 chr22: 37,423,086-37,425,612 MPST
    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
    nsv7024654copy number variation1nstd229human GRCh38 chr22: 36,352,908-37,059,696 , GRCh37.p13 chr22: 36,748,953-37,455,736 NCF4-AS1, TST, 23 more genes
    nsv6553934copy number variation1nstd223human GRCh38 chr22: 37,018,501-37,024,800 , GRCh37.p13 chr22: 37,414,542-37,420,841 MPST, TST
    nsv6549038copy number variation1nstd223human GRCh38 chr22: 36,979,385-37,039,093 , GRCh37.p13 chr22: 37,375,426-37,435,133 MPST, LOC112268295, 2 more genes
    nsv6311192copy number variation2nstd102humanUncertain significance GRCh37 chr22: 37,257,214-37,414,773 , GRCh38.p12 chr22: 36,861,172-37,018,732 CSF2RBP1, LOC105373022, 8 more genes
    nsv6134212copy number variation1nstd213human GRCh37 chr22: 36,430,000-39,960,001 , GRCh38.p12 chr22: 36,033,952-39,563,996 ATF4, COX5BP7, 133 more genes
    nsv5538974copy number variation1nstd206human GRCh38 chr22: 37,019,286-37,024,652 , GRCh37.p13 chr22: 37,415,327-37,420,693 MPST, TST
    nsv5360553translocation1nstd200human GRCh38 chr22: 37,024,652-37,024,652 , GRCh38 chr22: 37,019,286-37,019,286 , GRCh37.p13 chr22: 37,420,693-37,420,693 , GRCh37.p13 chr22: 37,415,327-37,415,327 MPST, TST
    nsv5339444translocation1nstd200human GRCh37 chr22: 37,420,693-37,420,693 , GRCh37 chr22: 37,415,327-37,415,327 , GRCh38.p12 chr22: 37,019,286-37,019,286 , GRCh38.p12 chr22: 37,024,652-37,024,652 TST, MPST
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