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Items: 1 to 20 of 175

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7061959inversion1nstd229human GRCh38 chr22: 36,818,005-44,993,640 , GRCh37.p13 chr22: 37,214,049-45,389,520 SMIM45, A4GALT, 271 more genes
    nsv7058316inversion1nstd229human GRCh38 chr22: 42,908,363-43,806,601 , GRCh37.p13 chr22: 43,304,369-44,202,481 LINC01639, LOC100419506, 18 more genes
    nsv7032203copy number variation1nstd229human GRCh38 chr22: 43,113,098-43,137,111 , GRCh37.p13 chr22: 43,509,104-43,533,117 BIK, MCAT
    nsv7030285copy number variation1nstd229human GRCh38 chr22: 43,135,987-43,138,616 , GRCh37.p13 chr22: 43,531,993-43,534,622 MCAT
    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
    nsv7024734copy number variation1nstd229human GRCh38 chr22: 43,130,969-43,149,666 , GRCh37.p13 chr22: 43,526,975-43,545,672 MCAT, TSPO
    nsv7023268copy number variation1nstd229human GRCh38 chr22: 42,944,893-43,176,363 , GRCh37.p13 chr22: 43,340,899-43,572,369 TTLL1-AS1, PACSIN2, 6 more genes
    nsv7022394copy number variation1nstd229human GRCh38 chr22: 43,136,788-43,164,687 , GRCh37.p13 chr22: 43,532,794-43,560,693 TTLL12, MCAT, 1 more genes
    nsv6638073copy number variation1nstd102humanPathogenic GRCh37 chr22: 43,436,847-51,188,164 , GRCh38.p12 chr22: 43,040,841-50,749,736 SCUBE1-AS1, MIR6821, 165 more genes
    nsv6535893copy number variation1nstd223human GRCh38 chr22: 41,572,303-44,198,988 , GRCh37.p13 chr22: 41,968,307-44,594,868 , RPS25P10, 87 more genes
    nsv6314059copy number variation1nstd102humanPathogenic GRCh37 chr22: 42,972,719-51,197,838 , GRCh38.p12 chr22: 42,576,713-50,759,410 TRABD, LOC100422416, 181 more genes
    nsv6313968copy number variation1nstd102humanPathogenic GRCh37 chr22: 43,451,316-46,662,660 , GRCh38.p12 chr22: 43,055,310-46,266,763 EFCAB6-DT, LOC107985535, 82 more genes
    nsv6291515copy number variation1nstd102humanUncertain significance GRCh37 chr22: 43,474,124-44,159,427 , GRCh38.p12 chr22: 43,078,118-43,763,547 RPS25P10, TSPO, 15 more genes
    nsv6291468copy number variation1nstd102humanUncertain significance GRCh37 chr22: 42,955,615-43,866,280 , GRCh38.p12 chr22: 42,559,609-43,470,400 POLDIP3, RPS25P10, 28 more genes
    nsv6290298copy number variation1nstd102humanPathogenic GRCh37 chr22: 42,321,321-51,244,066 , GRCh38.p12 chr22: 41,925,317-50,805,638 CERK, LINC01315, 212 more genes
    nsv6134214copy number variation1nstd213human GRCh37 chr22: 40,070,000-44,960,001 , GRCh38.p12 chr22: 39,673,995-44,564,121 , ACO2, 148 more genes
    nsv6134068copy number variation1nstd213human GRCh37 chr22: 43,520,000-44,290,001 , GRCh38.p12 chr22: 43,123,994-43,894,121 , BIK, 18 more genes
    nsv6056067copy number variation1nstd212human GRCh38 chr22: 43,142,477-43,143,221 , GRCh37.p13 chr22: 43,538,483-43,539,227 MCAT
    nsv5870167copy number variation1nstd209human GRCh38 chr22: 43,118,402-43,130,671 , GRCh37.p13 chr22: 43,514,408-43,526,677 MCAT, BIK
    nsv5673276copy number variation1nstd102humanPathogenic GRCh37 chr22: 42,440,000-43,780,000 , GRCh38.p12 chr22: 42,043,996-43,383,994 RPL5P34, ARFGAP3, 48 more genes
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