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Items: 1 to 20 of 319

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7098932copy number variation1nstd102humanUncertain significance GRCh38 chr9: 46,587-273,160 , GRCh37.p13 chr9: 46,587-273,160 FOXD4, PGM5P3, 7 more genes
    nsv7065614inversion1nstd229human GRCh38 chr9: 102,865-4,490,246 , GRCh37.p13 chr9: 102,865-4,490,246 RFX3, LOC102723803, 52 more genes
    nsv7064334inversion1nstd229human GRCh38 chr9: 85,493-2,205,560 , GRCh37.p13 chr9: 85,493-2,205,560 FOXD4, LOC105375942, 30 more genes
    nsv7060744inversion1nstd229human GRCh38 chr9: 98,219-202,799 , GRCh37.p13 chr9: 98,219-202,799 ZNG1A, LINC01388, 3 more genes
    nsv6876410copy number variation1nstd229human GRCh38 chr9: 91,778-350,405 , GRCh37.p13 chr9: 91,778-350,405 LOC105375942, FOXD4, 5 more genes
    nsv6875203copy number variation1nstd229human GRCh38 chr9: 45,723-296,268 , GRCh37.p13 chr9: 45,723-296,268 DOCK8, PGM5P3-AS1, 7 more genes
    nsv6873248copy number variation1nstd229human GRCh38 chr9: 86,623-258,649 , GRCh37.p13 chr9: 86,623-258,649 ZNG1A, LINC01388, 6 more genes
    nsv6872784copy number variation1nstd229human GRCh38 chr9: 61,391-264,481 , GRCh37.p13 chr9: 61,391-264,481 LOC105375943, LINC01388, 7 more genes
    nsv6871807copy number variation1nstd229human GRCh38 chr9: 61,252-340,894 , GRCh37.p13 chr9: 61,252-340,894 PGM5P3, ZNG1A, 7 more genes
    nsv6867261copy number variation1nstd229human GRCh38 chr9: 88,445-258,457 , GRCh37.p13 chr9: 88,445-258,457 FOXD4, ZNG1A, 6 more genes
    nsv6866770copy number variation1nstd229human GRCh38 chr9: 95,722-281,266 , GRCh37.p13 chr9: 95,722-281,266 LINC01388, DOCK8, 5 more genes
    nsv6862556copy number variation1nstd229human GRCh38 chr9: 107,262-259,446 , GRCh37.p13 chr9: 107,262-259,446 LOC105375943, DOCK8, 5 more genes
    nsv6859159copy number variation1nstd229human GRCh38 chr9: 87,991-237,441 , GRCh37.p13 chr9: 87,991-237,441 LOC105375942, FOXD4, 6 more genes
    nsv6634409copy number variation1nstd102humanLikely pathogenic GRCh37 chr9: 1-40,036,525 , GRCh38.p12 chr9: 10,001-39,445,729 ACO1, PLIN2, 594 more genes
    nsv6435466copy number variation1nstd223human GRCh38 chr9: 42,223-258,291 , GRCh37.p13 chr9: 42,223-258,291 FOXD4, ZNG1A, 7 more genes
    nsv6433848copy number variation1nstd223human GRCh38 chr9: 77,037-422,972 , GRCh37.p13 chr9: 77,037-422,972 LOC105375943, LINC01388, 7 more genes
    nsv6433523copy number variation1nstd223human GRCh38 chr9: 41,133-300,048 , GRCh37.p13 chr9: 41,133-300,048 ZNG1A, PGM5P3, 7 more genes
    nsv6432571copy number variation1nstd223human GRCh38 chr9: 118,801-125,700 , GRCh37.p13 chr9: 118,801-125,700 FOXD4, ZNG1A
    nsv6431769copy number variation1nstd223human GRCh38 chr9: 44,061-373,599 , GRCh37.p13 chr9: 44,061-373,599 FOXD4, PGM5P3, 8 more genes
    nsv6428594copy number variation1nstd223human GRCh38 chr9: 88,177-397,624 , GRCh37.p13 chr9: 88,177-397,624 DOCK8, FOXD4, 7 more genes
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