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Items: 1 to 20 of 523

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148254copy number variation1nstd102humanPathogenic GRCh38 chr17: 165,730-11,404,096 , GRCh37.p13 chr17: 396,627-11,307,413 RFLNB, C17orf100, 401 more genes
    nsv7073912inversion1nstd229human GRCh38 chr17: 1,213,690-8,318,220 , GRCh37.p13 chr17: 1,116,984-8,221,538 TNFSF12, SCARNA21, 321 more genes
    nsv7073657inversion1nstd229human GRCh38 chr17: 3,848,628-8,774,303 , GRCh37.p13 chr17: 3,751,922-8,677,621 LOC107987245, TRI-AAT5-5, 243 more genes
    nsv7072656inversion1nstd229human GRCh38 chr17: 4,280,481-4,388,405 , GRCh37.p13 chr17: 4,183,776-4,291,700 MFSD1P1, UBE2G1, 1 more genes
    nsv7070745inversion1nstd229human GRCh38 chr17: 4,137,958-4,492,235 , GRCh37.p13 chr17: 4,041,252-4,395,530 SPNS3, ZZEF1, 8 more genes
    nsv7067711inversion1nstd229human GRCh38 chr17: 4,286,801-4,441,831 , GRCh37.p13 chr17: 4,190,096-4,345,126 SPNS3, RN7SL774P, 2 more genes
    nsv7059571inversion1nstd229human GRCh38 chr17: 4,304,123-4,480,324 , GRCh37.p13 chr17: 4,207,418-4,383,619 RN7SL774P, UBE2G1, 1 more genes
    nsv6997822copy number variation1nstd229human GRCh38 chr17: 4,360,080-4,526,090 , GRCh37.p13 chr17: 4,263,375-4,429,385 UBE2G1, SPNS2, 3 more genes
    nsv6997184copy number variation1nstd229human GRCh38 chr17: 3,896,021-4,616,821 , GRCh37.p13 chr17: 3,799,315-4,520,116 RN7SL774P, LINC01996, 20 more genes
    nsv6993024copy number variation1nstd229human GRCh38 chr17: 4,350,810-4,352,811 , GRCh37.p13 chr17: 4,254,105-4,256,106 UBE2G1
    nsv6992155copy number variation1nstd229human GRCh38 chr17: 4,353,262-4,364,861 , GRCh37.p13 chr17: 4,256,557-4,268,156 RN7SL774P, UBE2G1
    nsv6991771copy number variation1nstd229human GRCh38 chr17: 4,267,596-4,267,669 , GRCh37.p13 chr17: 4,170,891-4,170,964 UBE2G1
    nsv6991432copy number variation1nstd229human GRCh38 chr17: 4,319,319-4,324,897 , GRCh37.p13 chr17: 4,222,614-4,228,192 UBE2G1
    nsv6991212copy number variation1nstd229human GRCh38 chr17: 4,362,295-4,524,160 , GRCh37.p13 chr17: 4,265,590-4,427,455 RN7SL774P, SPNS2-AS1, 3 more genes
    nsv6991148copy number variation1nstd229human GRCh38 chr17: 4,194,111-4,484,063 , GRCh37.p13 chr17: 4,097,406-4,387,358 RN7SL774P, SPNS3, 5 more genes
    nsv6987551copy number variation1nstd229human GRCh38 chr17: 4,290,557-4,295,931 , GRCh37.p13 chr17: 4,193,852-4,199,226 UBE2G1
    nsv6986923copy number variation1nstd229human GRCh38 chr17: 4,305,078-4,305,846 , GRCh37.p13 chr17: 4,208,373-4,209,141 UBE2G1
    nsv6985417copy number variation1nstd229human GRCh38 chr17: 4,323,934-4,327,958 , GRCh37.p13 chr17: 4,227,229-4,231,253 UBE2G1
    nsv6984278copy number variation1nstd229human GRCh38 chr17: 4,314,407-4,322,660 , GRCh37.p13 chr17: 4,217,702-4,225,955 UBE2G1
    nsv6982963copy number variation1nstd229human GRCh38 chr17: 4,196,063-4,502,773 , GRCh37.p13 chr17: 4,099,358-4,406,068 LOC100420060, RN7SL774P, 7 more genes
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