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Items: 1 to 20 of 178

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7145711copy number variation1nstd232human GRCh37.p13 chr22: 39,753,672-39,753,721 , GRCh38.p12 chr22: 39,357,667-39,357,716 SYNGR1
    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
    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
    nsv7059576inversion1nstd229human GRCh38 chr22: 39,383,299-39,387,852 , GRCh37.p13 chr22: 39,779,304-39,783,857 SYNGR1
    nsv7058666inversion1nstd229human GRCh38 chr22: 39,066,437-42,707,681 , GRCh37.p13 chr22: 39,462,442-43,103,687 LOC101927344, ATF4, 128 more genes
    nsv7031001copy number variation1nstd229human GRCh38 chr22: 39,372,235-39,418,111 , GRCh37.p13 chr22: 39,768,240-39,814,116 SYNGR1, TAB1
    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
    nsv6599726inversion1nstd223human GRCh38 chr22: 39,383,299-39,387,860 , GRCh37.p13 chr22: 39,779,304-39,783,865 SYNGR1
    nsv6596534inversion1nstd223human GRCh38 chr22: 39,133,553-42,757,193 , GRCh37.p13 chr22: 39,529,558-43,153,199 POLR3H, ACO2, 123 more genes
    nsv6554659copy number variation1nstd223human GRCh38 chr22: 39,385,964-39,386,875 , GRCh37.p13 chr22: 39,781,969-39,782,880 SYNGR1
    nsv6549249copy number variation1nstd223human GRCh38 chr22: 39,347,849-39,348,453 , GRCh37.p13 chr22: 39,743,854-39,744,458 SYNGR1
    nsv6545631copy number variation1nstd223human GRCh38 chr22: 39,385,941-39,387,925 , GRCh37.p13 chr22: 39,781,946-39,783,930 SYNGR1
    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
    nsv6220656copy number variation1nstd214human GRCh38 chr22: 39,357,667-39,357,716 , GRCh37.p13 chr22: 39,753,672-39,753,721 SYNGR1
    nsv6214390copy number variation1nstd214human GRCh38 chr22: 39,357,599-39,357,660 , GRCh37.p13 chr22: 39,753,604-39,753,665 SYNGR1
    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
    nsv6128775copy number variation1nstd186human GRCh37 chr22: 39,743,875-39,744,421 , GRCh38.p12 chr22: 39,347,870-39,348,416 SYNGR1
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