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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7097148copy number variation1nstd102humanPathogenic GRCh37 chr5: 52,285,299-56,189,507 , GRCh38.p12 chr5: 52,989,469-56,893,680 RPL37P25, CCNO, 69 more genes
    nsv7056095inversion1nstd229human GRCh38 chr5: 52,719,057-53,664,749 , GRCh37.p13 chr5: 52,014,891-52,960,579 B3GNTL1P1, RPL17P21, 11 more genes
    nsv7051121inversion1nstd229human GRCh38 chr5: 53,084,159-53,084,290 , GRCh37.p13 chr5: 52,379,989-52,380,120 ITGA2
    nsv6775592copy number variation1nstd229human GRCh38 chr5: 53,062,901-53,072,500 , GRCh37.p13 chr5: 52,358,731-52,368,330 ITGA2
    nsv6772401copy number variation1nstd229human GRCh38 chr5: 52,988,064-53,017,214 , GRCh37.p13 chr5: 52,283,894-52,313,044 ITGA2
    nsv6766352copy number variation1nstd229human GRCh38 chr5: 52,086,933-59,394,572 , GRCh37.p13 chr5: 51,382,767-58,690,398 , LOC105378980, 102 more genes
    nsv6759250copy number variation1nstd229human GRCh38 chr5: 53,066,847-53,073,612 , GRCh37.p13 chr5: 52,362,677-52,369,442 ITGA2
    nsv6630353copy number variation1nstd224human GRCh37 chr5: 51,952,084-52,464,757 , GRCh38.p12 chr5: 52,656,250-53,168,927 ITGA1, ITGA2, 5 more genes
    nsv6573962inversion1nstd223human GRCh38 chr5: 53,033,215-53,033,922 , GRCh37.p13 chr5: 52,329,045-52,329,752 ITGA2
    nsv6556420inversion1nstd223human GRCh38 chr5: 53,018,950-53,019,841 , GRCh37.p13 chr5: 52,314,780-52,315,671 ITGA2
    nsv6415450copy number variation1nstd223human GRCh38 chr5: 53,039,901-53,042,700 , GRCh37.p13 chr5: 52,335,731-52,338,530 ITGA2
    nsv6414120copy number variation1nstd223human GRCh38 chr5: 52,984,801-52,992,200 , GRCh37.p13 chr5: 52,280,631-52,288,030 ITGA2
    nsv6406324copy number variation1nstd223human GRCh38 chr5: 53,046,401-53,047,300 , GRCh37.p13 chr5: 52,342,231-52,343,130 ITGA2
    nsv6405149copy number variation1nstd223human GRCh38 chr5: 53,076,229-53,076,828 , GRCh37.p13 chr5: 52,372,059-52,372,658 ITGA2
    nsv6402281copy number variation1nstd223human GRCh38 chr5: 53,089,032-53,089,297 , GRCh37.p13 chr5: 52,384,862-52,385,127 ITGA2
    nsv6136122copy number variation1nstd213human GRCh37 chr5: 49,450,000-52,510,001 , GRCh38.p12 chr5: 50,154,166-53,214,171 , ISL1, 28 more genes
    nsv6135669copy number variation1nstd213human GRCh37 chr5: 49,470,000-58,470,001 , GRCh38.p12 chr5: 50,174,166-59,174,175 , ASS1P9, 120 more genes
    nsv6135419copy number variation1nstd213human GRCh37 chr5: 52,380,000-52,550,001 , GRCh38.p12 chr5: 53,084,170-53,254,171 ITGA2, MOCS2, 2 more genes
    nsv6135416copy number variation1nstd213human GRCh37 chr5: 50,510,000-68,870,001 , GRCh38.p12 chr5: 51,214,166-69,574,174 , TRIM23, 243 more genes
    nsv5897704copy number variation1nstd209human GRCh37.p13 chr5: 51,758,667-52,335,868 , GRCh38 chr5: 52,462,833-53,040,038 , ITGA1, 6 more genes
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