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Items: 1 to 20 of 193

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7074626inversion1nstd229human GRCh38 chr9: 113,105,118-113,230,133 , GRCh37.p13 chr9: 115,867,398-115,992,413 SLC31A1, FKBP15, 4 more genes
    nsv6876598copy number variation1nstd229human GRCh38 chr9: 113,239,638-113,254,077 , GRCh37.p13 chr9: 116,001,918-116,016,357 LOC107987119, SLC31A1
    nsv6873910copy number variation1nstd229human GRCh38 chr9: 113,230,654-113,236,364 , GRCh37.p13 chr9: 115,992,934-115,998,644 LOC107987119, SLC31A1
    nsv6872870copy number variation1nstd229human GRCh38 chr9: 113,251,224-113,251,415 , GRCh37.p13 chr9: 116,013,504-116,013,695 LOC107987119, SLC31A1
    nsv6871778copy number variation1nstd229human GRCh38 chr9: 113,245,327-113,249,650 , GRCh37.p13 chr9: 116,007,607-116,011,930 LOC107987119, SLC31A1
    nsv6863631copy number variation1nstd229human GRCh38 chr9: 113,185,401-113,334,700 , GRCh37.p13 chr9: 115,947,681-116,096,980 RNF183, FKBP15, 5 more genes
    nsv6862207copy number variation1nstd229human GRCh38 chr9: 113,240,756-113,243,701 , GRCh37.p13 chr9: 116,003,036-116,005,981 LOC107987119, SLC31A1
    nsv6859417copy number variation1nstd229human GRCh38 chr9: 113,240,788-113,241,018 , GRCh37.p13 chr9: 116,003,068-116,003,298 LOC107987119, SLC31A1
    nsv6858251copy number variation1nstd229human GRCh38 chr9: 113,228,626-113,239,091 , GRCh37.p13 chr9: 115,990,906-116,001,371 LOC107987119, SLC31A1
    nsv6634454copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-131,603,223 , GRCh38.p12 chr9: 203,861-128,840,944 HNRNPA1P41, GAS1RR, 1868 more genes
    nsv6633305copy number variation1nstd224human GRCh37 chr9: 115,861,201-116,125,789 , GRCh38.p12 chr9: 113,098,921-113,363,509 SLC31A2, BSPRY, 9 more genes
    nsv6568305inversion1nstd223human GRCh38 chr9: 113,248,310-113,248,565 , GRCh37.p13 chr9: 116,010,590-116,010,845 LOC107987119, SLC31A1
    nsv6567241inversion1nstd223human GRCh38 chr9: 113,264,667-113,265,543 , GRCh37.p13 chr9: 116,026,947-116,027,823 CDC26, SLC31A1
    nsv6565934inversion1nstd223human GRCh38 chr9: 113,264,593-113,265,631 , GRCh37.p13 chr9: 116,026,873-116,027,911 SLC31A1, CDC26
    nsv6451634copy number variation1nstd223human GRCh38 chr9: 113,245,327-113,249,645 , GRCh37.p13 chr9: 116,007,607-116,011,925 LOC107987119, SLC31A1
    nsv6451450copy number variation1nstd223human GRCh38 chr9: 113,232,787-113,233,156 , GRCh37.p13 chr9: 115,995,067-115,995,436 SLC31A1, LOC107987119
    nsv6451158copy number variation1nstd223human GRCh38 chr9: 113,261,244-113,264,209 , GRCh37.p13 chr9: 116,023,524-116,026,489 SLC31A1
    nsv6315405copy number variation1nstd102humanUncertain significance GRCh37 chr9: 19,356,861-119,513,311 , GRCh38.p12 chr9: 19,356,863-116,751,032 RNU6-156P, GDA, 1425 more genes
    nsv6314062copy number variation1nstd102humanLikely pathogenic GRCh37 chr9: 109,265,628-117,650,999 , GRCh38.p12 chr9: 106,503,347-114,888,719 ALAD, AMBP, 151 more genes
    nsv6313987copy number variation1nstd102humanUncertain significance GRCh37 chr9: 115,883,313-116,179,965 , GRCh38.p12 chr9: 113,121,033-113,417,685 HDHD3, BSPRY, 11 more genes
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