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Items: 1 to 20 of 554

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148253copy number variation1nstd102humanPathogenic GRCh38 chr8: 449,893-23,854,904 , GRCh37.p13 chr8: 399,893-23,712,417 ENTPD4, LOC100421446, 447 more genes
    nsv7148131copy number variation1nstd102humanPathogenic GRCh37 chr8: 10,501-11,142,629 , GRCh38.p12 chr8: 60,501-11,285,120 XKR6, FAM90A11, 224 more genes
    nsv7148128copy number variation1nstd102humanLikely pathogenic GRCh37 chr8: 10,501-6,614,959 , GRCh38.p12 chr8: 60,501-6,757,438 ANGPT2, CLN8, 67 more genes
    nsv7068644inversion1nstd229human GRCh38 chr8: 496,129-6,118,991 , GRCh37.p13 chr8: 446,129-5,976,513 LOC105377795, LOC100131395, 47 more genes
    nsv7067098inversion1nstd229human GRCh38 chr8: 489,642-489,725 , GRCh37.p13 chr8: 439,642-439,725 TDRP
    nsv7059594inversion1nstd229human GRCh38 chr8: 441,112-6,103,891 , GRCh37.p13 chr8: 391,112-5,961,413 LOC286083, MIR3674, 48 more genes
    nsv7059572inversion1nstd229human GRCh38 chr8: 310,007-766,676 , GRCh37.p13 chr8: 260,007-716,676 LOC105377773, FBXO25, 5 more genes
    nsv7058829inversion1nstd229human GRCh38 chr8: 299,298-502,102 , GRCh37.p13 chr8: 249,298-452,102 FAM87A, LOC105377773, 2 more genes
    nsv7058257inversion1nstd229human GRCh38 chr8: 494,042-494,143 , GRCh37.p13 chr8: 444,042-444,143 TDRP
    nsv6837769copy number variation1nstd229human GRCh38 chr8: 368,047-489,167 , GRCh37.p13 chr8: 318,047-439,167 FBXO25, TDRP, 1 more genes
    nsv6837124copy number variation1nstd229human GRCh38 chr8: 524,018-551,790 , GRCh37.p13 chr8: 474,018-501,790 TDRP
    nsv6836505copy number variation1nstd229human GRCh38 chr8: 542,103-641,763 , GRCh37.p13 chr8: 492,103-591,763 ERICH1, TDRP
    nsv6836467copy number variation1nstd229human GRCh38 chr8: 542,037-542,436 , GRCh37.p13 chr8: 492,037-492,436 TDRP
    nsv6835930copy number variation1nstd229human GRCh38 chr8: 398,644-490,398 , GRCh37.p13 chr8: 348,644-440,398 FBXO25, TDRP
    nsv6835590copy number variation1nstd229human GRCh38 chr8: 506,388-524,228 , GRCh37.p13 chr8: 456,388-474,228 TDRP
    nsv6834867copy number variation1nstd229human GRCh38 chr8: 476,298-808,142 , GRCh37.p13 chr8: 426,298-758,142 ERICH1, DLGAP2, 3 more genes
    nsv6834663copy number variation1nstd229human GRCh38 chr8: 530,487-538,943 , GRCh37.p13 chr8: 480,487-488,943 TDRP
    nsv6833213copy number variation1nstd229human GRCh38 chr8: 531,703-591,282 , GRCh37.p13 chr8: 481,703-541,282 TDRP
    nsv6831973copy number variation1nstd229human GRCh38 chr8: 429,138-637,937 , GRCh37.p13 chr8: 379,138-587,937 ERICH1, TDRP, 1 more genes
    nsv6830711copy number variation1nstd229human GRCh38 chr8: 545,843-574,728 , GRCh37.p13 chr8: 495,843-524,728 TDRP
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