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Items: 1 to 20 of 334

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7147563insertion1nstd232human GRCh37.p13 chr11: 46,811,737-46,811,737 , GRCh38.p12 chr11: 46,790,187-46,790,187 CKAP5
    nsv7146559insertion1nstd232human GRCh37.p13 chr11: 46,822,854-46,822,854 , GRCh38.p12 chr11: 46,801,304-46,801,304 CKAP5
    nsv7146098insertion1nstd232human GRCh37.p13 chr11: 46,772,161-46,772,161 , GRCh38.p12 chr11: 46,750,611-46,750,611 CKAP5
    nsv7145990insertion1nstd232human GRCh37.p13 chr11: 46,831,052-46,831,052 , GRCh38.p12 chr11: 46,809,502-46,809,502 CKAP5
    nsv7145178copy number variation1nstd232human GRCh37.p13 chr11: 46,772,805-46,772,894 , GRCh38.p12 chr11: 46,751,255-46,751,344 CKAP5, MIR5582
    nsv7144592insertion1nstd232human GRCh37.p13 chr11: 46,817,328-46,817,328 , GRCh38.p12 chr11: 46,795,778-46,795,778 CKAP5
    nsv7143278insertion1nstd232human GRCh37.p13 chr11: 46,766,129-46,766,129 , GRCh38.p12 chr11: 46,744,579-46,744,579 CKAP5
    nsv7142252insertion1nstd232human GRCh37.p13 chr11: 46,832,731-46,832,731 , GRCh38.p12 chr11: 46,811,181-46,811,181 CKAP5
    nsv7138182copy number variation1nstd232human GRCh37.p13 chr11: 46,771,982-46,772,075 , GRCh38.p12 chr11: 46,750,432-46,750,525 CKAP5
    nsv7137306insertion1nstd232human GRCh37.p13 chr11: 46,776,619-46,776,619 , GRCh38.p12 chr11: 46,755,069-46,755,069 CKAP5
    nsv7076407inversion1nstd229human GRCh38 chr11: 46,405,448-49,855,596 , GRCh37.p13 chr11: 46,426,998-49,862,647 KBTBD4, MADD-AS1, 89 more genes
    nsv6916349copy number variation1nstd229human GRCh38 chr11: 46,832,843-46,834,825 , GRCh37.p13 chr11: 46,854,394-46,856,376 CKAP5
    nsv6914061copy number variation1nstd229human GRCh38 chr11: 46,735,564-46,745,681 , GRCh37.p13 chr11: 46,757,114-46,767,231 CKAP5, F2
    nsv6913122copy number variation1nstd229human GRCh38 chr11: 46,806,797-46,922,858 , GRCh37.p13 chr11: 46,828,347-46,944,409 LRP4, CKAP5, 1 more genes
    nsv6912956copy number variation1nstd229human GRCh38 chr11: 46,617,201-46,758,300 , GRCh37.p13 chr11: 46,638,751-46,779,850 F2, ZNF408, 5 more genes
    nsv6912711copy number variation1nstd229human GRCh38 chr11: 46,431,488-46,810,907 , GRCh37.p13 chr11: 46,453,038-46,832,457 AMBRA1, ARHGAP1, 9 more genes
    nsv6912086copy number variation1nstd229human GRCh38 chr11: 46,786,938-47,006,817 , GRCh37.p13 chr11: 46,808,488-47,028,368 LRP4, CSTPP1, 2 more genes
    nsv6910252copy number variation1nstd229human GRCh38 chr11: 46,359,860-46,749,716 , GRCh37.p13 chr11: 46,381,410-46,771,266 AMBRA1, ARHGAP1, 12 more genes
    nsv6905349copy number variation1nstd229human GRCh38 chr11: 46,829,794-46,832,133 , GRCh37.p13 chr11: 46,851,345-46,853,684 CKAP5
    nsv6904690copy number variation1nstd229human GRCh38 chr11: 46,675,001-46,743,300 , GRCh37.p13 chr11: 46,696,551-46,764,850 CKAP5, ATG13, 3 more genes
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