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Items: 1 to 20 of 106

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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
    nsv7069304inversion1nstd229human GRCh38 chr22: 41,294,727-42,750,704 , GRCh37.p13 chr22: 41,690,731-43,146,710 SERHL2, CSDC2, 63 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
    nsv7036552copy number variation1nstd229human GRCh38 chr22: 41,712,735-41,727,878 , GRCh37.p13 chr22: 42,108,739-42,123,882 RNU6ATAC22P, MEI1
    nsv7031860copy number variation1nstd229human GRCh38 chr22: 41,721,116-41,734,591 , GRCh37.p13 chr22: 42,117,120-42,130,595 RNU6ATAC22P, MEI1
    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
    nsv7024371copy number variation1nstd229human GRCh38 chr22: 41,703,667-41,810,262 , GRCh37.p13 chr22: 42,099,671-42,206,266 HMGN2P10, CCDC134, 2 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
    nsv6554600copy number variation1nstd223human GRCh38 chr22: 41,721,412-41,721,887 , GRCh37.p13 chr22: 42,117,416-42,117,891 RNU6ATAC22P, MEI1
    nsv6548525copy number variation1nstd223human GRCh38 chr22: 41,721,189-41,723,466 , GRCh37.p13 chr22: 42,117,193-42,119,470 MEI1, RNU6ATAC22P
    nsv6545368copy number variation1nstd223human GRCh38 chr22: 41,718,999-41,721,239 , GRCh37.p13 chr22: 42,115,003-42,117,243 MEI1, RNU6ATAC22P
    nsv6537706copy number variation1nstd223human GRCh38 chr22: 41,689,561-41,802,762 , GRCh37.p13 chr22: 42,085,565-42,198,766 SNU13, HMGN2P10, 4 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
    nsv6311137copy number variation1nstd102humanUncertain significance GRCh37 chr22: 41,277,754-43,089,957 , GRCh38.p12 chr22: 40,881,750-42,693,951 RRP7A, OGFRP1, 79 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
    nsv6134067copy number variation1nstd213human GRCh37 chr22: 40,070,000-43,110,001 , GRCh38.p12 chr22: 39,673,995-42,713,995 ACO2, ADSL, 106 more genes
    nsv5540416copy number variation1nstd206human GRCh38 chr22: 41,717,440-41,721,022 , GRCh37.p13 chr22: 42,113,444-42,117,026 RNU6ATAC22P, MEI1
    nsv5534625copy number variation1nstd206human GRCh38 chr22: 41,712,554-41,721,313 , GRCh37.p13 chr22: 42,108,558-42,117,317 RNU6ATAC22P, MEI1
    nsv5383177mobile element deletion1nstd186human GRCh37 chr22: 42,117,265-42,117,568 , GRCh38.p12 chr22: 41,721,261-41,721,564 RNU6ATAC22P, MEI1
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