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Items: 1 to 20 of 245

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7064652inversion1nstd229human GRCh38 chr22: 43,155,814-43,155,862 , GRCh37.p13 chr22: 43,551,820-43,551,868 TSPO
    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
    nsv7035223copy number variation1nstd229human GRCh38 chr22: 43,145,006-43,151,090 , GRCh37.p13 chr22: 43,541,012-43,547,096 TSPO
    nsv7032592copy number variation1nstd229human GRCh38 chr22: 43,151,893-43,152,635 , GRCh37.p13 chr22: 43,547,899-43,548,641 TSPO
    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
    nsv7027228copy number variation1nstd229human GRCh38 chr22: 43,153,014-43,153,085 , GRCh37.p13 chr22: 43,549,020-43,549,091 TSPO
    nsv7024734copy number variation1nstd229human GRCh38 chr22: 43,130,969-43,149,666 , GRCh37.p13 chr22: 43,526,975-43,545,672 MCAT, TSPO
    nsv7024035copy number variation1nstd229human GRCh38 chr22: 43,159,143-43,161,138 , GRCh37.p13 chr22: 43,555,149-43,557,144 TSPO
    nsv7023274copy number variation1nstd229human GRCh38 chr22: 43,162,027-43,166,376 , GRCh37.p13 chr22: 43,558,033-43,562,382 TTLL12, 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
    nsv7022719copy number variation1nstd229human GRCh38 chr22: 43,153,339-43,153,667 , GRCh37.p13 chr22: 43,549,345-43,549,673 TSPO
    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
    nsv7021834copy number variation1nstd229human GRCh38 chr22: 43,153,019-43,181,630 , GRCh37.p13 chr22: 43,549,025-43,577,636 TTLL12, TSPO
    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
    nsv6553309copy number variation1nstd223human GRCh38 chr22: 43,153,019-43,181,623 , GRCh37.p13 chr22: 43,549,025-43,577,629 TSPO, TTLL12
    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
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