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Items: 1 to 20 of 195

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7065657inversion1nstd229human GRCh38 chr13: 76,225,150-84,243,039 , GRCh37.p13 chr13: 76,799,286-84,817,174 HSPD1P8, ELOCP23, 85 more genes
    nsv7064310inversion1nstd229human GRCh38 chr13: 83,826,788-85,042,039 , GRCh37.p13 chr13: 84,400,923-85,616,174 SLITRK1, UBE2D3P4, 9 more genes
    nsv7064226inversion1nstd229human GRCh38 chr13: 79,480,333-84,336,702 , GRCh37.p13 chr13: 80,054,468-84,910,837 LINC01038, LOC105370287, 32 more genes
    nsv7061790inversion1nstd229human GRCh38 chr13: 76,348,646-84,254,120 , GRCh37.p13 chr13: 76,922,782-84,828,255 LINC01068, LOC105370264, 83 more genes
    nsv6950966copy number variation1nstd229human GRCh38 chr13: 83,877,658-83,928,522 , GRCh37.p13 chr13: 84,451,793-84,502,657 SLITRK1, VENTXP2
    nsv6946961copy number variation1nstd229human GRCh38 chr13: 83,850,714-83,878,030 , GRCh37.p13 chr13: 84,424,849-84,452,165 SLITRK1
    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
    nsv6634431copy number variation1nstd102humanPathogenic GRCh37 chr13: 19,253,848-115,108,937 , GRCh38.p12 chr13: 18,679,708-114,343,462 MTUS2-AS1, LOC105370213, 1330 more genes
    nsv6484870copy number variation1nstd223human GRCh38 chr13: 83,874,830-83,875,418 , GRCh37.p13 chr13: 84,448,965-84,449,553 SLITRK1
    nsv6479775copy number variation1nstd223human GRCh38 chr13: 77,934,952-83,910,114 , GRCh37.p13 chr13: 78,509,087-84,484,249 LINC01069, LOC105370274, 54 more genes
    nsv6315495copy number variation1nstd102humanPathogenic GRCh37 chr13: 1-115,169,878 , GRCh38.p12 chr13: 18,445,862-114,344,403 RNU6-80P, EFNB2, 1334 more genes
    nsv6314172copy number variation1nstd102humanPathogenic GRCh37 chr13: 75,574,661-87,784,831 , GRCh38.p12 chr13: 75,000,524-87,132,576 LMO7, TBC1D4, 119 more genes
    nsv6314171copy number variation1nstd102humanPathogenic GRCh37 chr13: 79,370,012-115,107,733 , GRCh38.p12 chr13: 78,795,877-114,342,258 MIR4705, LOC102724149, 430 more genes
    nsv6314030copy number variation1nstd102humanPathogenic GRCh37 chr13: 19,436,286-114,981,726 , GRCh38.p12 chr13: 18,862,146-114,216,251 RPSAP53, LOC105370213, 1310 more genes
    nsv6313904copy number variation1nstd102humanPathogenic GRCh37 chr13: 78,514,567-115,107,733 , GRCh38.p12 chr13: 77,940,432-114,342,258 LOC101927284, LOC105370330, 444 more genes
    nsv6291752copy number variation1nstd102humanPathogenic GRCh37 chr13: 59,574,760-89,410,027 , GRCh38.p12 chr13: 59,000,626-88,757,773 GYG1P2, LOC102723968, 284 more genes
    nsv6291487copy number variation1nstd102humanPathogenic GRCh37 chr13: 42,504,540-108,206,269 , GRCh38.p12 chr13: 41,930,404-107,553,921 CALM2P4, RNU6-81P, 778 more genes
    nsv6289999copy number variation1nstd102humanPathogenic GRCh37 chr13: 1-115,169,878 , GRCh38.p12 chr13: 18,445,862-114,344,403 LINC00363, LOC105370118, 1334 more genes
    nsv6132663copy number variation1nstd213human GRCh37 chr13: 67,680,000-86,760,001 , GRCh38.p12 chr13: 67,105,868-86,185,866 KLF5, BTF3P11, 187 more genes
    nsv5932186copy number variation1nstd209human GRCh38 chr13: 77,934,881-83,910,012 , GRCh37.p13 chr13: 78,509,016-84,484,147 NDFIP2, LINC01068, 54 more genes
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