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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    esv2505420copy number variation1estd197human NCBI36 chr17: 44,024,246-44,024,246 , GRCh37.p13 chr17: 46,669,247-46,669,247 , GRCh38.p12 chr17: 48,591,885-48,591,885 HOXB5, HOXB-AS3
    esv2000537copy number variation1estd194human NCBI36 chr17: 44,024,246-44,024,247 , GRCh37.p13 chr17: 46,669,247-46,669,248 , GRCh38.p12 chr17: 48,591,885-48,591,886 HOXB5, HOXB-AS3
    esv1514065insertion1estd22human NCBI36 chr17: 44,023,194-44,023,194 , GRCh37.p13 chr17: 46,668,195-46,668,195 , GRCh38.p12 chr17: 48,590,833-48,590,833 HOXB5, HOXB-AS3
    nsv1878569short tandem repeat1nstd128human GRCh37 chr17: 46,669,041-46,669,064 , GRCh38.p12 chr17: 48,591,679-48,591,702 HOXB5, HOXB-AS3
    nsv1877988short tandem repeat1nstd128human GRCh37 chr17: 46,669,351-46,669,365 , GRCh38.p12 chr17: 48,591,989-48,592,003 HOXB5, HOXB-AS3
    nsv1878570short tandem repeat3nstd128human GRCh37 chr17: 46,669,247-46,669,259 , GRCh38.p12 chr17: 48,591,885-48,591,897 HOXB5, HOXB-AS3
    nsv3112840copy number variation1nstd145human GRCh37 chr17: 46,666,661-46,671,289 , GRCh38.p12 chr17: 48,589,299-48,593,927 HOXB5, HOXB3, 2 more genes
    esv3396513copy number variation2estd59human NCBI36 chr17: 44,026,269-44,026,656 , GRCh37.p13 chr17: 46,671,270-46,671,657 , GRCh38.p12 chr17: 48,593,908-48,594,295 HOXB5, HOXB6, 1 more genes
    nsv6289076insertion1nstd214human GRCh37.p13 chr17: 46,666,847-46,666,847 , GRCh38 chr17: 48,589,485-48,589,485 HOXB5, HOXB3, 1 more genes
    esv2950452insertion1estd209human GRCh37 chr17: 46,671,195-46,671,195 , GRCh38.p12 chr17: 48,593,833-48,593,833 HOXB5, HOXB6, 1 more genes
    esv2950451insertion1estd209human GRCh37 chr17: 46,671,195-46,671,195 , GRCh38.p12 chr17: 48,593,833-48,593,833 HOXB5, HOXB6, 1 more genes
    esv2018534insertion1estd194human NCBI36 chr17: 44,026,195-44,026,195 , GRCh37.p13 chr17: 46,671,196-46,671,196 , GRCh38.p12 chr17: 48,593,834-48,593,834 HOXB5, HOXB6, 1 more genes
    nsv7058105inversion1nstd229human GRCh38 chr17: 48,590,046-48,595,764 , GRCh37.p13 chr17: 46,667,408-46,673,126 HOXB5, HOXB3, 2 more genes
    esv3814104complex chromosomal rearrangement3estd192human GRCh37 chr15: 90,658,118-90,658,138 , GRCh37 chr17: 46,669,477-46,669,497 , GRCh38.p12 chr15: 90,114,886-90,114,906 , GRCh38.p12 chr17: 48,592,115-48,592,135 HOXB5, HOXB-AS3, 1 more genes
    nsv3911811copy number variation1nstd102humanPathogenic NCBI36 chr17: 31,824,931-78,654,742 , GRCh37.p13 chr17: 34,750,818-81,048,189 , GRCh38.p12 chr17: 36,382,248-83,103,577 HOXB5, PRPSAP1, 1350 more genes
    nsv3911757copy number variation1nstd102humanPathogenic NCBI36 chr17: 43,419,251-44,761,758 , GRCh37 chr17: 46,064,252-47,406,759 , GRCh38 chr17: 47,986,886-49,329,397 HOXB5, LINC02086, 59 more genes
    nsv3913486copy number variation1nstd102humanPathogenic GRCh38 chr17: 48,520,885-49,511,208 , NCBI36 chr17: 43,953,246-44,943,569 , GRCh37 chr17: 46,598,247-47,588,570 HOXB5, MIR6165, 54 more genes
    nsv3903684copy number variation1nstd102humanPathogenic GRCh37 chr17: 8,547-81,060,040 , GRCh38.p12 chr17: 158,756-83,102,004 HOXB5, MIR3185, 2366 more genes
    nsv3899740copy number variation1nstd102humanPathogenic GRCh37 chr17: 7,214-81,058,310 , GRCh38.p12 chr17: 157,423-83,100,564 HOXB5, P4HB, 2366 more genes
    nsv3906245copy number variation1nstd102humanPathogenic GRCh37 chr17: 12,344-81,057,996 , GRCh38.p12 chr17: 162,553-83,100,251 HOXB5, MIR21, 2366 more genes
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