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Items: 1 to 20 of 401

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7098746copy number variation1nstd102humanPathogenic GRCh37 chr17: 56,786,681-56,797,331 , GRCh38.p12 chr17: 58,709,320-58,719,970 RAD51C
    nsv7098717copy number variation1nstd102humanPathogenic GRCh37 chr17: 56,782,798-56,819,433 , GRCh38.p12 chr17: 58,705,437-58,742,072 RAD51C, LOC105371843
    nsv7095346copy number variation1nstd102humanLikely pathogenic GRCh37 chr17: 56,811,469-56,811,583 , GRCh38.p12 chr17: 58,734,108-58,734,222 RAD51C, LOC105371843
    nsv7095345copy number variation1nstd102humanPathogenic GRCh37 chr17: 56,787,200-56,787,371 , GRCh38.p12 chr17: 58,709,839-58,710,010 RAD51C
    nsv7095344copy number variation2nstd102humanPathogenic, Likely pathogenic GRCh37 chr17: 56,780,547-56,787,361 , GRCh38.p12 chr17: 58,703,186-58,710,000 RAD51C
    nsv7095172copy number variation1nstd102humanUncertain significance GRCh37 chr17: 56,798,087-57,771,213 , GRCh38.p12 chr17: 58,720,726-59,693,852 LINC01476, RNU2-58P, 22 more genes
    nsv7062151inversion1nstd229human GRCh38 chr17: 58,705,434-61,610,111 , GRCh37.p13 chr17: 56,782,795-59,687,472 RNU4-13P, LOC105371850, 74 more genes
    nsv6996520copy number variation1nstd229human GRCh38 chr17: 58,688,348-58,691,028 , GRCh37.p13 chr17: 56,765,709-56,768,389 RAD51C, TEX14
    nsv6996436copy number variation1nstd229human GRCh38 chr17: 58,691,101-58,700,600 , GRCh37.p13 chr17: 56,768,462-56,777,961 TEX14, RAD51C
    nsv6994787copy number variation1nstd229human GRCh38 chr17: 58,733,972-58,743,655 , GRCh37.p13 chr17: 56,811,333-56,821,016 RAD51C, LOC105371843
    nsv6989343copy number variation1nstd229human GRCh38 chr17: 58,700,305-58,704,636 , GRCh37.p13 chr17: 56,777,666-56,781,997 RAD51C
    nsv6984598copy number variation1nstd229human GRCh38 chr17: 58,542,080-58,875,342 , GRCh37.p13 chr17: 56,619,441-56,952,703 LOC107985048, RNU1-108P, 11 more genes
    nsv6983415copy number variation1nstd229human GRCh38 chr17: 58,721,050-58,735,406 , GRCh37.p13 chr17: 56,798,411-56,812,767 LOC105371843, RAD51C
    nsv6978849copy number variation1nstd229human GRCh38 chr17: 58,709,301-58,713,840 , GRCh37.p13 chr17: 56,786,662-56,791,201 RAD51C
    nsv6978816copy number variation1nstd229human GRCh38 chr17: 58,703,294-58,703,393 , GRCh37.p13 chr17: 56,780,655-56,780,754 RAD51C
    nsv6634560copy number variation1nstd102humanPathogenic GRCh38 chr17: 58,694,984-58,695,038 , GRCh37 chr17: 56,772,345-56,772,399 RAD51C
    nsv6593106inversion1nstd223human GRCh38 chr17: 58,712,345-58,714,050 , GRCh37.p13 chr17: 56,789,706-56,791,411 RAD51C
    nsv6592478inversion1nstd223human GRCh38 chr17: 58,697,484-58,698,025 , GRCh37.p13 chr17: 56,774,845-56,775,386 RAD51C
    nsv6592470inversion1nstd223human GRCh38 chr17: 58,715,832-58,716,713 , GRCh37.p13 chr17: 56,793,193-56,794,074 RAD51C
    nsv6589359inversion1nstd223human GRCh38 chr17: 58,700,922-58,701,495 , GRCh37.p13 chr17: 56,778,283-56,778,856 RAD51C
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