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Items: 1 to 20 of 204

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148201copy number variation1nstd102humanPathogenic GRCh38 chr3: 93,979,547-124,774,010 , GRCh37.p13 chr3: 93,698,391-124,492,857 NECTIN3, H2BP3, 418 more genes
    nsv7147710insertion1nstd232human GRCh37.p13 chr3: 113,442,943-113,442,943 , GRCh38.p12 chr3: 113,724,096-113,724,096 NAA50
    nsv7140560insertion1nstd232human GRCh37.p13 chr3: 113,442,388-113,442,388 , GRCh38.p12 chr3: 113,723,541-113,723,541 NAA50
    nsv7098849copy number variation1nstd102humanPathogenic GRCh37 chr3: 110,943,783-115,859,912 , GRCh38.p12 chr3: 111,224,936-116,141,065 ATG3, SIDT1, 81 more genes
    nsv7096435copy number variation1nstd102humanUncertain significance GRCh37 chr3: 113,010,404-114,099,634 , GRCh38.p12 chr3: 113,291,557-114,380,787 USF3, VPS26AP1, 27 more genes
    nsv7051524inversion1nstd229human GRCh38 chr3: 110,492,556-118,654,181 , GRCh37.p13 chr3: 110,211,403-118,373,028 MIR8076, ZBTB20-AS4, 106 more genes
    nsv7048325inversion1nstd229human GRCh38 chr3: 112,726,892-114,038,623 , GRCh37.p13 chr3: 112,445,739-113,757,470 CCDC191, RABGGTBP1, 28 more genes
    nsv7046766inversion1nstd229human GRCh38 chr3: 113,523,091-114,031,809 , GRCh37.p13 chr3: 113,241,938-113,750,656 SIDT1, ZDHHC23, 12 more genes
    nsv7039165inversion1nstd229human GRCh38 chr3: 113,732,797-113,732,857 , GRCh37.p13 chr3: 113,451,644-113,451,704 NAA50
    nsv6703311copy number variation1nstd229human GRCh38 chr3: 113,719,468-113,719,622 , GRCh37.p13 chr3: 113,438,315-113,438,469 NAA50
    nsv6702390copy number variation1nstd229human GRCh38 chr3: 113,740,191-113,933,212 , GRCh37.p13 chr3: 113,459,038-113,652,059 GRAMD1C, CTDNEP1P1, 4 more genes
    nsv6701576copy number variation1nstd229human GRCh38 chr3: 109,882,767-113,954,905 , GRCh37.p13 chr3: 109,601,614-113,673,752 SLC9C1, NECTIN3, 64 more genes
    nsv6636830copy number variation1nstd102humanPathogenic GRCh37 chr3: 107,059,705-115,005,256 , GRCh38.p12 chr3: 107,340,858-115,286,409 ATP6V1A, DRD3, 117 more genes
    nsv6568820inversion1nstd223human GRCh38 chr3: 113,729,569-113,730,112 , GRCh37.p13 chr3: 113,448,416-113,448,959 NAA50
    nsv6374098copy number variation1nstd223human GRCh38 chr3: 113,722,101-113,723,400 , GRCh37.p13 chr3: 113,440,948-113,442,247 NAA50
    nsv6363800copy number variation1nstd223human GRCh38 chr3: 113,740,191-113,933,199 , GRCh37.p13 chr3: 113,459,038-113,652,046 GRAMD1C, VPS26AP1, 4 more genes
    nsv6315408copy number variation1nstd102humanPathogenic GRCh37 chr3: 106,598,767-115,704,696 , GRCh38.p12 chr3: 106,879,920-115,985,849 DZIP3, MIR9900, 138 more genes
    nsv6134776copy number variation1nstd213human GRCh37 chr3: 105,120,000-116,510,001 , GRCh38.p12 chr3: 105,401,156-116,791,154 , ALCAM, 156 more genes
    nsv5453590copy number variation1nstd206human GRCh38 chr3: 113,723,542-113,723,958 , GRCh37.p13 chr3: 113,442,389-113,442,805 NAA50
    nsv5445908copy number variation1nstd206human GRCh38 chr3: 113,721,937-113,722,854 , GRCh37.p13 chr3: 113,440,784-113,441,701 NAA50
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