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Items: 1 to 20 of 155

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7096314copy number variation1nstd102humanPathogenic GRCh37 chr22: 42,456,283-43,089,957 , GRCh38.p12 chr22: 42,060,279-42,693,951 SERHL2, POLDIP3, 28 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
    nsv7058827inversion1nstd229human GRCh38 chr22: 42,518,031-42,753,421 , GRCh37.p13 chr22: 42,914,037-43,149,427 CYB5R3, A4GALT, 8 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
    nsv7033765copy number variation1nstd229human GRCh38 chr22: 42,637,604-42,869,737 , GRCh37.p13 chr22: 43,033,610-43,265,743 PACSIN2, GOLGA2P4, 9 more genes
    nsv7029667copy number variation1nstd229human GRCh38 chr22: 42,618,303-42,784,193 , GRCh37.p13 chr22: 43,014,309-43,180,199 GOLGA2P4, RPL5P34, 3 more genes
    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
    nsv7022743copy number variation1nstd229human GRCh38 chr22: 42,632,843-42,638,066 , GRCh37.p13 chr22: 43,028,849-43,034,072 CYB5R3, ATP5MGL
    nsv6637527copy number variation1nstd102humanUncertain significance GRCh37 chr22: 42,765,874-43,059,475 , GRCh38.p12 chr22: 42,369,868-42,663,469 SERHL2, SERHL, 11 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
    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
    nsv6311325copy number variation1nstd102humanUncertain significance GRCh37 chr22: 43,015,779-43,089,957 , GRCh38.p12 chr22: 42,619,773-42,693,951 CYB5R3, A4GALT, 1 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
    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
    nsv6277945copy number variation1nstd214human GRCh38 chr22: 42,640,245-42,640,321 , GRCh37.p13 chr22: 43,036,251-43,036,327 CYB5R3, ATP5MGL
    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
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