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Items: 1 to 20 of 235

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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
    nsv7037763copy number variation1nstd229human GRCh38 chr22: 41,637,878-41,642,085 , GRCh37.p13 chr22: 42,033,882-42,038,089 XRCC6
    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
    nsv7024007copy number variation1nstd229human GRCh38 chr22: 41,639,900-41,671,542 , GRCh37.p13 chr22: 42,035,904-42,067,546 XRCC6
    nsv6598227inversion1nstd223human GRCh38 chr22: 41,622,935-41,623,071 , GRCh37.p13 chr22: 42,018,939-42,019,075 XRCC6
    nsv6597241inversion1nstd223human GRCh38 chr22: 41,623,680-41,624,243 , GRCh37.p13 chr22: 42,019,684-42,020,247 XRCC6
    nsv6596534inversion1nstd223human GRCh38 chr22: 39,133,553-42,757,193 , GRCh37.p13 chr22: 39,529,558-43,153,199 POLR3H, ACO2, 123 more genes
    nsv6541328copy number variation1nstd223human GRCh38 chr22: 41,622,301-41,624,800 , GRCh37.p13 chr22: 42,018,305-42,020,804 XRCC6
    nsv6538203copy number variation1nstd223human GRCh38 chr22: 41,624,016-41,626,388 , GRCh37.p13 chr22: 42,020,020-42,022,392 XRCC6
    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
    nsv6207644copy number variation1nstd214human GRCh38 chr22: 41,631,453-41,631,608 , GRCh37.p13 chr22: 42,027,457-42,027,612 XRCC6
    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
    nsv6111938insertion1nstd212human GRCh38 chr22: 41,643,424-41,643,424 , GRCh37.p13 chr22: 42,039,428-42,039,428 XRCC6
    nsv6050108copy number variation1nstd212human GRCh38 chr22: 41,645,772-41,645,849 , GRCh37.p13 chr22: 42,041,776-42,041,853 XRCC6
    nsv6046644copy number variation1nstd212human GRCh38 chr22: 41,624,415-41,624,722 , GRCh37.p13 chr22: 42,020,419-42,020,726 XRCC6
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