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Items: 1 to 20 of 152

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7099034copy number variation1nstd102humanPathogenic GRCh37 chr11: 66,274,870-66,292,647 , GRCh38.p12 chr11: 66,507,399-66,525,176 DPP3, BBS1, 1 more genes
    nsv7094096copy number variation1nstd102humanUncertain significance GRCh37 chr11: 66,099,747-66,291,373 , GRCh38.p12 chr11: 66,332,276-66,523,902 LOC100505524, BRMS1, 14 more genes
    nsv7094093copy number variation2nstd102humanUncertain significance GRCh37 chr11: 64,973,914-70,052,579 , GRCh38.p12 chr11: 65,206,443-70,206,473 B4GAT1, CHKA-DT, 208 more genes
    nsv7093406copy number variation1nstd102humanUncertain significance GRCh37 chr11: 66,178,392-66,433,436 , GRCh38.p12 chr11: 66,410,921-66,665,965 MRPL11, NPAS4, 15 more genes
    nsv7064487inversion1nstd229human GRCh38 chr11: 66,481,370-66,483,259 , GRCh37.p13 chr11: 66,248,841-66,250,730 DPP3
    nsv7061947inversion1nstd229human GRCh38 chr11: 66,494,296-66,563,130 , GRCh37.p13 chr11: 66,261,767-66,330,601 CTSF, DPP3, 3 more genes
    nsv6910540copy number variation1nstd229human GRCh38 chr11: 66,498,773-66,524,032 , GRCh37.p13 chr11: 66,266,244-66,291,503 BBS1, ZDHHC24, 1 more genes
    nsv6909691copy number variation1nstd229human GRCh38 chr11: 66,488,332-66,488,530 , GRCh37.p13 chr11: 66,255,803-66,256,001 DPP3
    nsv6908016copy number variation1nstd229human GRCh38 chr11: 66,482,408-66,510,431 , GRCh37.p13 chr11: 66,249,879-66,277,902 BBS1, DPP3
    nsv6905877copy number variation1nstd229human GRCh38 chr11: 60,405,001-68,536,600 , GRCh37.p13 chr11: 60,172,474-68,304,068 INCENP, SNRPCP12, 409 more genes
    nsv6904468copy number variation1nstd229human GRCh38 chr11: 66,499,128-66,501,964 , GRCh37.p13 chr11: 66,266,599-66,269,435 DPP3
    nsv6579186inversion1nstd223human GRCh38 chr11: 66,498,362-66,500,188 , GRCh37.p13 chr11: 66,265,833-66,267,659 DPP3
    nsv6473296copy number variation1nstd223human GRCh38 chr11: 66,499,128-66,501,916 , GRCh37.p13 chr11: 66,266,599-66,269,387 DPP3
    nsv6464198copy number variation1nstd223human GRCh38 chr11: 66,498,801-66,524,000 , GRCh37.p13 chr11: 66,266,272-66,291,471 ZDHHC24, BBS1, 1 more genes
    nsv6459179copy number variation1nstd223human GRCh38 chr11: 66,502,878-66,503,246 , GRCh37.p13 chr11: 66,270,349-66,270,717 DPP3
    nsv6315537copy number variation1nstd102humanPathogenic GRCh37 chr11: 32,799,481-134,938,470 , GRCh38.p12 chr11: 32,777,935-135,068,576 PYGM, ATL3, 2125 more genes
    nsv6314192copy number variation1nstd102humanUncertain significance GRCh37 chr11: 64,935,724-66,405,514 , GRCh38.p12 chr11: 65,168,253-66,638,043 CNIH2, GAL3ST3, 95 more genes
    nsv6314012copy number variation1nstd102humanUncertain significance GRCh37 chr11: 66,188,172-66,402,747 , GRCh38.p12 chr11: 66,420,701-66,635,276 LOC100505524, ZDHHC24, 13 more genes
    nsv6309121copy number variation2nstd102humanPathogenic GRCh37 chr11: 64,522,783-66,283,694 , GRCh38.p12 chr11: 64,755,311-66,516,223 SF3B2, ZNRD2-DT, 124 more genes
    nsv6290938copy number variation1nstd102humanUncertain significance GRCh37 chr11: 65,963,737-66,581,485 , GRCh38.p12 chr11: 66,196,266-66,814,014 CCS, RN7SL12P, 38 more genes
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