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Items: 1 to 20 of 324

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148239copy number variation1nstd102humanPathogenic GRCh38 chr13: 98,343,655-110,990,677 , GRCh37.p13 chr13: 98,995,909-111,643,024 CLYBL-AS3, PPIAP24, 162 more genes
    nsv7148164copy number variation1nstd102humanPathogenic GRCh38 chr13: 106,425,676-114,326,445 , GRCh37.p13 chr13: 107,078,024-115,085,141 TUBGCP3, LINC01043, 132 more genes
    nsv7094235copy number variation1nstd102humanUncertain significance GRCh37 chr13: 110,959,271-111,279,914 , GRCh38.p12 chr13: 110,306,924-110,627,567 RAB20, NAXD, 5 more genes
    nsv7094068copy number variation1nstd102humanUncertain significance GRCh37 chr13: 111,286,872-111,319,840 , GRCh38.p12 chr13: 110,634,525-110,667,493 NAXD, CARS2
    nsv7093990copy number variation1nstd102humanPathogenic GRCh37 chr13: 111,268,022-111,274,733 , GRCh38.p12 chr13: 110,615,675-110,622,386 NAXD
    nsv7074580inversion1nstd229human GRCh38 chr13: 110,243,158-113,630,621 , GRCh37.p13 chr13: 110,895,505-114,284,936 LINC01070, NAXD, 71 more genes
    nsv7060236inversion1nstd229human GRCh38 chr13: 109,400,177-111,221,158 , GRCh37.p13 chr13: 110,052,524-111,873,505 LINC00399, ANKRD10, 36 more genes
    nsv7059605inversion1nstd229human GRCh38 chr13: 110,238,294-111,024,734 , GRCh37.p13 chr13: 110,890,641-111,677,081 COL4A1, RPL21P107, 17 more genes
    nsv7058406inversion1nstd229human GRCh38 chr13: 110,594,743-110,640,532 , GRCh37.p13 chr13: 111,247,090-111,292,879 NAXD, CARS2
    nsv6957827copy number variation1nstd229human GRCh38 chr13: 110,400,001-110,889,200 , GRCh37.p13 chr13: 111,052,348-111,541,547 COL4A2-AS2, COL4A2, 12 more genes
    nsv6957375copy number variation1nstd229human GRCh38 chr13: 110,294,204-110,633,816 , GRCh37.p13 chr13: 110,946,551-111,286,163 RAB20, MIR8073, 5 more genes
    nsv6954592copy number variation1nstd229human GRCh38 chr13: 110,322,299-111,271,113 , GRCh37.p13 chr13: 110,974,646-111,923,460 ARHGEF7-AS2, LINC00567, 22 more genes
    nsv6949698copy number variation1nstd229human GRCh38 chr13: 110,608,503-110,613,467 , GRCh37.p13 chr13: 111,260,850-111,265,814 NAXD
    nsv6946826copy number variation1nstd229human GRCh38 chr13: 110,514,328-110,681,153 , GRCh37.p13 chr13: 111,166,675-111,333,500 NAXD, RAB20, 1 more genes
    nsv6945314copy number variation1nstd229human GRCh38 chr13: 110,480,701-110,676,500 , GRCh37.p13 chr13: 111,133,048-111,328,847 RAB20, COL4A2, 3 more genes
    nsv6943503copy number variation1nstd229human GRCh38 chr13: 110,623,198-110,636,417 , GRCh37.p13 chr13: 111,275,545-111,288,764 NAXD
    nsv6941418copy number variation1nstd229human GRCh38 chr13: 110,424,301-110,677,100 , GRCh37.p13 chr13: 111,076,648-111,329,447 NAXD, RAB20, 4 more genes
    nsv6941399copy number variation1nstd229human GRCh38 chr13: 110,509,601-110,716,200 , GRCh37.p13 chr13: 111,161,948-111,368,547 NAXD, RAB20, 3 more genes
    nsv6638047copy number variation1nstd102humanPathogenic GRCh37 chr13: 75,268,539-115,107,733 , GRCh38.p12 chr13: 74,694,402-114,342,258 CUL4A, LOC105370373, 488 more genes
    nsv6637400copy number variation1nstd102humanPathogenic GRCh37 chr13: 97,142,120-115,107,733 , GRCh38.p12 chr13: 96,489,866-114,342,258 LOC107984609, LINC00354, 265 more genes
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