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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
    nsv7077764inversion1nstd229human GRCh38 chr22: 37,971,370-41,589,449 , GRCh37.p13 chr22: 38,367,377-41,985,453 UQCRFS1P1, LOC105373027, 119 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
    nsv7058666inversion1nstd229human GRCh38 chr22: 39,066,437-42,707,681 , GRCh37.p13 chr22: 39,462,442-43,103,687 LOC101927344, ATF4, 128 more genes
    nsv7033584copy number variation1nstd229human GRCh38 chr22: 39,527,477-39,531,486 , GRCh37.p13 chr22: 39,923,482-39,927,491 RPS19BP1
    nsv7027741copy number variation1nstd229human GRCh38 chr22: 39,432,386-49,047,389 , GRCh37.p13 chr22: 39,828,391-49,443,201 LOC105373064, ACO2, 233 more genes
    nsv7023009copy number variation1nstd229human GRCh38 chr22: 39,523,326-39,527,640 , GRCh37.p13 chr22: 39,919,331-39,923,645 RPS19BP1
    nsv7020429copy number variation1nstd229human GRCh38 chr22: 39,407,096-39,566,174 , GRCh37.p13 chr22: 39,803,101-39,962,179 MGAT3-AS1, RPS19BP1, 6 more genes
    nsv6637214copy number variation1nstd102humanUncertain significance GRCh37 chr22: 39,768,795-41,946,225 , GRCh38.p12 chr22: 39,372,790-41,550,221 MRTFA-AS1, LOC105373043, 62 more genes
    nsv6626954copy number variation1nstd224human GRCh37 chr22: 39,907,318-40,563,020 , GRCh38.p12 chr22: 39,511,313-40,167,016 ATF4, MIEF1, 12 more genes
    nsv6596534inversion1nstd223human GRCh38 chr22: 39,133,553-42,757,193 , GRCh37.p13 chr22: 39,529,558-43,153,199 POLR3H, ACO2, 123 more genes
    nsv6311136copy number variation1nstd102humanUncertain significance GRCh37 chr22: 39,621,728-41,077,932 , GRCh38.p12 chr22: 39,225,723-40,681,928 TAB1, TNRC6B, 34 more genes
    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
    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
    nsv5668975insertion1nstd207human GRCh38 chr22: 39,531,978-39,531,978 , GRCh37.p13 chr22: 39,927,983-39,927,983 RPS19BP1
    nsv5360583translocation1nstd200human GRCh38 chr22: 39,527,979-39,527,979 , GRCh38 chr22: 39,528,047-39,528,047 , GRCh37.p13 chr22: 39,924,052-39,924,052 , GRCh37.p13 chr22: 39,923,984-39,923,984 RPS19BP1
    nsv5288097copy number variation1nstd204human GRCh38.p13 chr22: 38,982,101-39,534,900 , GRCh37.p13 chr22: 39,378,106-39,930,905 APOBEC3C, COX5BP7, 25 more genes
    nsv5038486copy number variation1nstd200human GRCh38 chr22: 39,486,153-39,539,517 , GRCh37.p13 chr22: 39,882,158-39,935,522 RPS19BP1, LOC105373035, 3 more genes
    nsv4882825copy number variation1nstd200human GRCh37 chr22: 39,882,158-39,935,522 , GRCh38.p12 chr22: 39,486,153-39,539,517 MIEF1, ATF4, 3 more genes
    nsv4729926copy number variation1nstd102humanPathogenic GRCh37 chr22: 16,197,005-51,224,252 , GRCh38.p12 chr22: 16,367,190-50,785,824 FBXO7, GTSE1, 1084 more genes
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