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Items: 1 to 20 of 348

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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
    nsv7061790inversion1nstd229human GRCh38 chr13: 76,348,646-84,254,120 , GRCh37.p13 chr13: 76,922,782-84,828,255 LINC01068, LOC105370264, 83 more genes
    nsv6951330copy number variation1nstd229human GRCh38 chr13: 78,625,984-78,631,224 , GRCh37.p13 chr13: 79,200,119-79,205,359 OBI1
    nsv6944702copy number variation1nstd229human GRCh38 chr13: 78,628,859-78,634,367 , GRCh37.p13 chr13: 79,202,994-79,208,502 OBI1
    nsv6940459copy number variation1nstd229human GRCh38 chr13: 78,586,001-78,614,300 , GRCh37.p13 chr13: 79,160,136-79,188,435 LOC780529, OBI1-AS1, 2 more genes
    nsv6939964copy number variation1nstd229human GRCh38 chr13: 78,609,537-78,613,157 , GRCh37.p13 chr13: 79,183,672-79,187,292 OBI1, OBI1-AS1
    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
    nsv6637820copy number variation1nstd102humanUncertain significance GRCh37 chr13: 79,099,535-80,675,355 , GRCh38.p12 chr13: 78,525,400-80,101,220 LINC00382, CCT5-2P, 21 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
    nsv6595109inversion1nstd223human GRCh38 chr13: 78,656,630-78,656,730 , GRCh37.p13 chr13: 79,230,765-79,230,865 OBI1
    nsv6590121inversion1nstd223human GRCh38 chr13: 78,656,229-78,656,796 , GRCh37.p13 chr13: 79,230,364-79,230,931 OBI1
    nsv6583507inversion1nstd223human GRCh38 chr13: 78,633,829-78,634,531 , GRCh37.p13 chr13: 79,207,964-79,208,666 OBI1
    nsv6492384copy number variation1nstd223human GRCh38 chr13: 78,616,424-78,616,917 , GRCh37.p13 chr13: 79,190,559-79,191,052 OBI1-AS1, OBI1
    nsv6486107copy number variation1nstd223human GRCh38 chr13: 78,628,901-78,634,400 , GRCh37.p13 chr13: 79,203,036-79,208,535 OBI1
    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
    nsv6314117copy number variation1nstd102humanPathogenic GRCh37 chr13: 36,376,204-80,681,753 , GRCh38.p12 chr13: 35,802,067-80,107,618 RBM26, RNY4P31, 591 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
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