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Items: 1 to 20 of 352

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7076337inversion1nstd229human GRCh38 chr9: 93,520,425-93,520,588 , GRCh37.p13 chr9: 96,282,707-96,282,870 FAM120A
    nsv7071727inversion1nstd229human GRCh38 chr9: 93,332,022-93,605,636 , GRCh37.p13 chr9: 96,094,304-96,367,918 FAM120AOS, FAM120A2P, 6 more genes
    nsv7070830inversion1nstd229human GRCh38 chr9: 93,462,794-93,462,840 , GRCh37.p13 chr9: 96,225,076-96,225,122 FAM120A
    nsv6875312copy number variation1nstd229human GRCh38 chr9: 93,460,221-93,461,441 , GRCh37.p13 chr9: 96,222,503-96,223,723 FAM120A
    nsv6868707copy number variation1nstd229human GRCh38 chr9: 93,424,001-93,756,500 , GRCh37.p13 chr9: 96,186,283-96,518,782 LOC107987097, MIR548AU, 4 more genes
    nsv6866267copy number variation1nstd229human GRCh38 chr9: 93,520,429-93,520,931 , GRCh37.p13 chr9: 96,282,711-96,283,213 FAM120A
    nsv6866132copy number variation1nstd229human GRCh38 chr9: 93,451,384-93,451,449 , GRCh37.p13 chr9: 96,213,666-96,213,731 FAM120A, FAM120AOS
    nsv6860604copy number variation1nstd229human GRCh38 chr9: 93,518,201-93,526,700 , GRCh37.p13 chr9: 96,280,483-96,288,982 FAM120A
    nsv6859905copy number variation1nstd229human GRCh38 chr9: 93,482,308-93,482,463 , GRCh37.p13 chr9: 96,244,590-96,244,745 FAM120A
    nsv6637944copy number variation1nstd102humanPathogenic GRCh37 chr9: 95,711,603-98,469,214 , GRCh38.p12 chr9: 92,949,321-95,706,932 MIRLET7D, MIR24-1, 60 more genes
    nsv6634454copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-131,603,223 , GRCh38.p12 chr9: 203,861-128,840,944 HNRNPA1P41, GAS1RR, 1868 more genes
    nsv6560806inversion1nstd223human GRCh38 chr9: 93,472,096-93,473,165 , GRCh37.p13 chr9: 96,234,378-96,235,447 FAM120A
    nsv6454210copy number variation1nstd223human GRCh38 chr9: 93,496,372-93,497,435 , GRCh37.p13 chr9: 96,258,654-96,259,717 FAM120A
    nsv6452658copy number variation1nstd223human GRCh38 chr9: 93,451,101-93,453,900 , GRCh37.p13 chr9: 96,213,383-96,216,182 FAM120AOS, FAM120A
    nsv6449399copy number variation1nstd223human GRCh38 chr9: 93,479,138-93,484,613 , GRCh37.p13 chr9: 96,241,420-96,246,895 FAM120A
    nsv6447755copy number variation1nstd223human GRCh38 chr9: 92,901,749-100,255,234 , GRCh37.p13 chr9: 95,664,031-103,017,516 EIF4BP3, VN1R51P, 162 more genes
    nsv6444335copy number variation1nstd223human GRCh38 chr9: 93,511,184-93,512,381 , GRCh37.p13 chr9: 96,273,466-96,274,663 FAM120A
    nsv6443079copy number variation1nstd223human GRCh38 chr9: 93,460,472-93,462,511 , GRCh37.p13 chr9: 96,222,754-96,224,793 FAM120A
    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
    nsv6315179copy number variation1nstd102humanPathogenic GRCh37 chr9: 93,864,974-106,661,581 , GRCh38.p12 chr9: 91,102,692-103,899,300 SUGT1P4-STRA6LP, NR4A3, 255 more genes
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