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Items: 1 to 20 of 128

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5554090sequence alteration1nstd206human GRCh38 chr17: 32,109,732-67,925,723 , GRCh37.p13 chr17: 30,436,751-65,921,839 , APOH, 1099 more genes
    nsv5519241copy number variation1nstd206human GRCh38 chr17: 35,928,931-35,929,520 , GRCh37.p13 chr17: 34,255,935-34,256,524 RDM1
    nsv5358829translocation1nstd200human GRCh38 chr17: 35,929,520-35,929,520 , GRCh38 chr17: 35,928,931-35,928,931 , GRCh37.p13 chr17: 34,255,935-34,255,935 , GRCh37.p13 chr17: 34,256,524-34,256,524 RDM1
    nsv5150568mobile element insertion1nstd203human GRCh38 chr17: 35,930,169-35,930,184 , GRCh37.p13 chr17: 34,257,173-34,257,188 RDM1
    nsv5016157copy number variation1nstd200human GRCh38 chr17: 35,921,066-35,922,202 , GRCh37.p13 chr17: 34,248,070-34,249,206 RDM1
    nsv4858675copy number variation1nstd200human GRCh37 chr17: 34,255,935-34,256,524 , GRCh38.p12 chr17: 35,928,931-35,929,520 , GRCh38.p12 chr17|NT_187614.1: 163,463-164,052 RDM1
    nsv4858674copy number variation1nstd200human GRCh37 chr17: 34,248,070-34,249,206 , GRCh38.p12 chr17: 35,921,066-35,922,202 , GRCh38.p12 chr17|NT_187614.1: 155,598-156,734 RDM1
    nsv4762422inversion1nstd199human GRCh37 chr17: 151-36,202,676 , GRCh38.p12 chr17: 150,358-36,446,544 , ABR, 1046 more genes
    nsv4675787copy number variation1nstd102humanUncertain significance GRCh37 chr17: 34,158,619-34,477,480 , GRCh38.p12 chr17: 35,919,249-36,150,098 , GRCh38.p12 chr17|NT_187614.1: 153,781-385,008 CCL4, CCL3-AS1, 15 more genes
    nsv4634127copy number variation1nstd183human GRCh37 chr17: 34,151,274-34,485,091 , GRCh38.p12 chr17: 35,919,249-36,157,718 , GRCh38.p12 chr17|NT_187614.1: 153,781-392,619 , RDM1, 16 more genes
    nsv4631441copy number variation1nstd183human GRCh37 chr17: 34,149,960-34,475,514 , GRCh38.p12 chr17: 35,919,249-36,148,133 , GRCh38.p12 chr17|NT_187614.1: 153,781-383,042 , CCL14, 16 more genes
    nsv4502247mobile element insertion1nstd166human GRCh37.p13 chr17: 34,249,505-34,249,505 , GRCh38.p12 chr17: 35,922,501-35,922,501 , GRCh38.p12 chr17|NT_187614.1: 157,033-157,033 RDM1
    nsv4457831copy number variation1nstd102humanPathogenic GRCh37 chr17: 21,690,653-38,772,647 , GRCh38.p12 chr17: 22,164,047-40,616,395 LOC105371753, TAOK1, 474 more genes
    nsv4457542copy number variation1nstd102humanUncertain significance GRCh37 chr17: 34,151,183-34,477,480 , GRCh38.p12 chr17: 35,919,249-36,150,098 , GRCh38.p12 chr17|NT_187614.1: 153,781-385,008 CCL14, LOC101927369, 15 more genes
    nsv4380150copy number variation1nstd173human GRCh37 chr17: 34,151,081-34,477,480 , GRCh38.p12 chr17: 35,919,249-36,150,098 , GRCh38.p12 chr17|NT_187614.1: 153,781-385,008 , CCL4, 16 more genes
    nsv4330632inversion1nstd166human GRCh37.p13 chr17: 18,838,526-72,042,289 , GRCh38.p12 chr17: 18,935,213-74,046,150 , ACACA, 1499 more genes
    nsv4244076copy number variation1nstd166human GRCh37.p13 chr17: 34,058,749-34,328,565 , GRCh38.p12 chr17: 35,731,730-35,919,248 , GRCh38.p12 chr17|NT_187614.1: 1-153,780 , CCL5, 13 more genes
    nsv4238083copy number variation1nstd166human GRCh37.p13 chr17: 34,255,824-34,256,524 , GRCh38.p12 chr17: 35,928,820-35,929,520 , GRCh38.p12 chr17|NT_187614.1: 163,352-164,052 RDM1
    nsv3919991copy number variation1nstd102humanUncertain significance NCBI36 chr17: 31,198,036-31,323,231 , GRCh37.p13 chr17|NW_004166864.2: 139,087-211,416 , GRCh37.p13 chr17: 34,173,923-34,299,118 , GRCh38.p12 chr17: 35,846,919-35,919,248 , GRCh38.p12 chr17|NT_187614.1: 81,451-153,780 HEATR9, LRRC37A9P, 7 more genes
    nsv3914783copy number variation1nstd102humanPathogenic NCBI36 chr17: 16,698,288-78,654,742 , GRCh37.p13 chr17: 16,757,563-81,048,189 , GRCh38.p12 chr17: 16,854,249-83,103,577 LOC105371922, GJD3, 1855 more genes
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