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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7098427copy number variation1nstd102humanUncertain significance GRCh37 chr9: 131,857,676-135,942,612 , GRCh38.p12 chr9: 129,095,397-133,067,225 ASS1, SETX, 86 more genes
    nsv7097932copy number variation1nstd102humanUncertain significance GRCh37 chr9: 133,884,602-135,942,612 , GRCh38.p12 chr9: 131,009,215-133,067,225 LAMC3, SPACA9, 40 more genes
    nsv7097690copy number variation1nstd102humanUncertain significance GRCh37 chr9: 131,087,402-141,016,451 , GRCh38.p12 chr9: 128,325,123-138,121,999 REXO4, TOR1B, 324 more genes
    nsv7075268inversion1nstd229human GRCh38 chr9: 128,672,751-137,526,572 , GRCh37.p13 chr9: 131,435,030-140,421,024 PNPLA7, NSMF, 293 more genes
    nsv7075196inversion1nstd229human GRCh38 chr9: 130,990,409-137,053,229 , GRCh37.p13 chr9: 133,865,796-139,947,681 LINC02907, LCN1, 196 more genes
    nsv7072738inversion1nstd229human GRCh38 chr9: 132,212,883-132,274,469 , GRCh37.p13 chr9: 135,088,270-135,149,856 SETX, NTNG2
    nsv7070509inversion1nstd229human GRCh38 chr9: 132,174,626-132,224,811 , GRCh37.p13 chr9: 135,050,013-135,100,198 NTNG2
    nsv7059760inversion1nstd229human GRCh38 chr9: 130,985,407-137,050,712 , GRCh37.p13 chr9: 133,860,794-139,945,164 LCN10, RAPGEF1, 196 more genes
    nsv6877784copy number variation1nstd229human GRCh38 chr9: 132,224,801-132,274,500 , GRCh37.p13 chr9: 135,100,188-135,149,887 SETX, NTNG2
    nsv6875916copy number variation1nstd229human GRCh38 chr9: 132,211,337-132,252,437 , GRCh37.p13 chr9: 135,086,724-135,127,824 NTNG2
    nsv6874325copy number variation1nstd229human GRCh38 chr9: 132,241,117-132,244,036 , GRCh37.p13 chr9: 135,116,504-135,119,423 NTNG2
    nsv6872957copy number variation1nstd229human GRCh38 chr9: 132,161,901-132,249,200 , GRCh37.p13 chr9: 135,037,288-135,124,587 NTNG2
    nsv6870780copy number variation1nstd229human GRCh38 chr9: 132,176,727-132,180,084 , GRCh37.p13 chr9: 135,052,114-135,055,471 NTNG2
    nsv6870349copy number variation1nstd229human GRCh38 chr9: 132,181,694-132,184,436 , GRCh37.p13 chr9: 135,057,081-135,059,823 NTNG2
    nsv6866355copy number variation1nstd229human GRCh38 chr9: 132,174,355-132,176,545 , GRCh37.p13 chr9: 135,049,742-135,051,932 NTNG2
    nsv6865560copy number variation1nstd229human GRCh38 chr9: 132,104,707-132,425,204 , GRCh37.p13 chr9: 134,980,094-135,300,591 CFAP77, SETX, 5 more genes
    nsv6864463copy number variation1nstd229human GRCh38 chr9: 132,171,279-132,173,461 , GRCh37.p13 chr9: 135,046,666-135,048,848 NTNG2
    nsv6863523copy number variation1nstd229human GRCh38 chr9: 132,238,018-132,248,427 , GRCh37.p13 chr9: 135,113,405-135,123,814 NTNG2
    nsv6863087copy number variation1nstd229human GRCh38 chr9: 132,169,608-132,210,372 , GRCh37.p13 chr9: 135,044,995-135,085,759 NTNG2
    nsv6863007copy number variation1nstd229human GRCh38 chr9: 132,233,563-132,235,701 , GRCh37.p13 chr9: 135,108,950-135,111,088 NTNG2
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