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Items: 1 to 20 of 178

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5926719copy number variation1nstd209human GRCh38 chr11: 104,936,696-104,976,069 , GRCh37.p13 chr11: 104,807,423-104,846,796 CASP4
    nsv5918104copy number variation1nstd209human GRCh38 chr11: 104,190,618-110,044,159 , GRCh37.p13 chr11: 104,061,346-109,914,884 , CARD18, 71 more genes
    nsv5865326copy number variation1nstd209human GRCh38 chr11: 104,956,281-104,958,680 , GRCh37.p13 chr11: 104,827,008-104,829,407 CASP4
    nsv5864818copy number variation2nstd209human GRCh38 chr11: 104,942,939-104,945,270 , GRCh37.p13 chr11: 104,813,666-104,815,997 CASP4
    nsv5852084copy number variation1nstd209human GRCh38 chr11: 104,936,639-104,952,638 , GRCh37.p13 chr11: 104,807,366-104,823,365 CASP4
    nsv5672640copy number variation1nstd102humanPathogenic GRCh37 chr11: 94,153,285-111,965,700 , GRCh38.p12 chr11: 94,420,119-112,094,976 HSPD1P13, CARD17P, 239 more genes
    nsv5380796copy number variation1nstd102humanPathogenic GRCh37 chr11: 11,835,569-118,373,112 , GRCh38.p12 chr11: 11,814,022-118,502,397 FAUP4, MMP7, 2031 more genes
    nsv5185563mobile element insertion1nstd203human GRCh38 chr11: 104,957,690-104,957,697 , GRCh37.p13 chr11: 104,828,417-104,828,424 CASP4
    nsv5139665mobile element insertion1nstd203human GRCh38 chr11: 104,945,270-104,945,284 , GRCh37.p13 chr11: 104,815,997-104,816,011 CASP4
    nsv4989250copy number variation1nstd200human GRCh38 chr11: 104,163,006-105,424,224 , GRCh37.p13 chr11: 104,033,734-105,294,951 LOC105369468, CASP1P1, 19 more genes
    nsv4712898copy number variation1nstd195human GRCh37 chr11: 104,797,151-104,887,101 , GRCh38.p12 chr11: 104,926,424-105,016,374 CASP4, CASP5
    nsv4680641copy number variation1nstd189human GRCh37.p13 chr11: 104,027,037-105,291,719 , GRCh38.p12 chr11: 104,156,309-105,420,992 CASP1, CASP4, 19 more genes
    nsv4680518copy number variation1nstd189human GRCh37.p13 chr11: 104,037,015-105,276,482 , GRCh38.p12 chr11: 104,166,287-105,405,755 CASP1, CASP4, 18 more genes
    nsv4680081copy number variation1nstd189human GRCh37.p13 chr11: 104,023,678-105,291,719 , GRCh38.p12 chr11: 104,152,950-105,420,992 CASP1, CASP4, 19 more genes
    nsv4676052copy number variation1nstd102humanUncertain significance GRCh37 chr11: 103,980,525-106,914,369 , GRCh38.p12 chr11: 104,109,797-107,043,643 CARD17P, LOC643855, 36 more genes
    nsv4675822copy number variation1nstd102humanLikely benign GRCh37 chr11: 104,805,250-105,062,846 , GRCh38.p12 chr11: 104,934,523-105,192,119 LOC107984381, CARD17P, 10 more genes
    nsv4675680copy number variation1nstd102humanPathogenic GRCh37 chr11: 103,320,065-114,349,787 , GRCh38.p12 chr11: 103,449,337-114,479,065 DRD2, NCAM1, 181 more genes
    nsv4675315copy number variation1nstd102humanLikely benign GRCh37 chr11: 104,032,889-105,292,804 , GRCh38.p12 chr11: 104,162,161-105,422,077 CASP1P3, RNA5SP348, 19 more genes
    nsv4675055copy number variation1nstd102humanUncertain significance GRCh37 chr11: 103,983,847-106,914,369 , GRCh38.p12 chr11: 104,113,119-107,043,643 LOC105369466, CASP4LP, 36 more genes
    nsv4675037copy number variation1nstd102humanLikely benign GRCh37 chr11: 104,714,600-104,828,745 , GRCh38.p12 chr11: 104,843,873-104,958,018 CASP4LP, CASP12, 2 more genes
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