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Items: 1 to 20 of 80

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7096799copy number variation1nstd102humanUncertain significance GRCh37 chr3: 38,180,153-38,618,292 , GRCh38.p12 chr3: 38,138,662-38,576,801 ACVR2B-AS1, SCN5A, 13 more genes
    nsv7051268inversion1nstd229human GRCh38 chr3: 37,000,362-39,352,689 , GRCh37.p13 chr3: 37,041,853-39,394,180 PLCD1, RNU6-1227P, 59 more genes
    nsv7048850inversion1nstd229human GRCh38 chr3: 37,408,411-39,634,596 , GRCh37.p13 chr3: 37,449,902-39,676,087 OXSR1, ITGA9, 55 more genes
    nsv7042103inversion1nstd229human GRCh38 chr3: 37,827,304-38,566,908 , GRCh37.p13 chr3: 37,868,795-38,608,399 SCN5A, CDC42P7, 22 more genes
    nsv7039010inversion1nstd229human GRCh38 chr3: 37,851,228-39,078,678 , GRCh37.p13 chr3: 37,892,719-39,120,169 CDC42P7, LOC105377033, 28 more genes
    nsv6709671copy number variation1nstd229human GRCh38 chr3: 33,814,589-38,161,211 , GRCh37.p13 chr3: 33,856,081-38,202,702 RFC3P1, ITGA9, 51 more genes
    nsv6705786copy number variation1nstd229human GRCh38 chr3: 38,070,501-38,146,100 , GRCh37.p13 chr3: 38,111,992-38,187,591 MYD88, ACAA1, 2 more genes
    nsv6705602copy number variation1nstd229human GRCh38 chr3: 38,118,477-38,166,986 , GRCh37.p13 chr3: 38,159,968-38,208,477 LOC105377033, MYD88, 4 more genes
    nsv6699688copy number variation1nstd229human GRCh38 chr3: 38,074,001-38,142,100 , GRCh37.p13 chr3: 38,115,492-38,183,591 LOC105377033, MYD88, 2 more genes
    nsv6545895inversion1nstd223human GRCh38 chr3: 38,143,453-38,149,845 , GRCh37.p13 chr3: 38,184,944-38,191,336 MYD88
    nsv6537958inversion1nstd223human GRCh38 chr3: 37,408,438-39,634,613 , GRCh37.p13 chr3: 37,449,929-39,676,104 ITGA9-AS1, MIR26A1, 55 more genes
    nsv6374659copy number variation1nstd223human GRCh38 chr3: 38,143,452-38,149,870 , GRCh37.p13 chr3: 38,184,943-38,191,361 MYD88
    nsv6313737copy number variation1nstd102humanUncertain significance GRCh37 chr3: 38,109,534-38,669,316 , GRCh38.p12 chr3: 38,068,043-38,627,825 ACVR2B-AS1, SCN5A, 16 more genes
    nsv6311982copy number variation1nstd102humanUncertain significance GRCh37 chr3: 37,034,542-38,835,501 , GRCh38.p12 chr3: 36,993,051-38,794,010 SCN10A, PPP2R2DP1, 41 more genes
    nsv6311966copy number variation1nstd102humanPathogenic GRCh37 chr3: 16,710,965-41,275,270 , GRCh38.p12 chr3: 16,669,458-41,233,779 LOC102724104, CRIP1P2, 291 more genes
    nsv6134845copy number variation1nstd213human GRCh37 chr3: 37,240,000-38,310,001 , GRCh38.p12 chr3: 37,198,509-38,268,510 ACAA1, GOLGA4, 22 more genes
    nsv5037434inversion1nstd200human GRCh38 chr3: 5,031,119-56,902,223 , GRCh37.p13 chr3: 5,072,804-56,936,251 , IRAK2, 925 more genes
    nsv5030280inversion1nstd200human GRCh38 chr3: 3,432,416-77,775,308 , GRCh37.p13 chr3: 3,474,100-77,824,459 , BHLHE40, 1198 more genes
    nsv4888770inversion1nstd200human GRCh37 chr3: 3,474,100-77,824,459 , GRCh38.p12 chr3: 3,432,416-77,775,308 , ATRIP, 1198 more genes
    nsv4877503inversion1nstd200human GRCh37 chr3: 24,885,632-100,711,157 , GRCh38.p12 chr3: 24,844,141-100,992,313 , LINC00692, 1088 more genes
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