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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7141879insertion1nstd232human GRCh37.p13 chr9: 98,266,015-98,266,015 , GRCh38.p12 chr9: 95,503,733-95,503,733 PTCH1
    nsv7137011copy number variation1nstd102humanUncertain significance GRCh38 chr9: 95,508,341-95,508,396 , GRCh37 chr9: 98,270,623-98,270,678 PTCH1
    nsv7077729inversion1nstd229human GRCh38 chr9: 94,417,509-96,970,614 , GRCh37.p13 chr9: 97,179,791-99,732,896 HSD17B3-AS1, ERCC6L2, 60 more genes
    nsv7075365inversion1nstd229human GRCh38 chr9: 94,549,389-100,549,990 , GRCh37.p13 chr9: 97,311,671-103,312,272 PCAT7, ANKS6, 128 more genes
    nsv7062168inversion1nstd229human GRCh38 chr9: 95,510,222-95,513,320 , GRCh37.p13 chr9: 98,272,504-98,275,602 PTCH1
    nsv7061823inversion1nstd229human GRCh38 chr9: 94,710,575-96,645,135 , GRCh37.p13 chr9: 97,472,857-99,407,417 LOC105376163, LINC00092, 42 more genes
    nsv6875757copy number variation1nstd229human GRCh38 chr9: 95,365,901-95,671,700 , GRCh37.p13 chr9: 98,128,183-98,433,982 LOC105376158, LOC105376155, 5 more genes
    nsv6873774copy number variation1nstd229human GRCh38 chr9: 95,485,099-95,485,137 , GRCh37.p13 chr9: 98,247,381-98,247,419 PTCH1
    nsv6872628copy number variation1nstd229human GRCh38 chr9: 94,768,901-95,577,300 , GRCh37.p13 chr9: 97,531,183-98,339,582 RPS26P37, MIR27B, 17 more genes
    nsv6870453copy number variation1nstd229human GRCh38 chr9: 95,503,733-95,504,063 , GRCh37.p13 chr9: 98,266,015-98,266,345 PTCH1
    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
    nsv6451077copy number variation1nstd223human GRCh38 chr9: 95,505,801-95,509,600 , GRCh37.p13 chr9: 98,268,083-98,271,882 PTCH1
    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
    nsv6446414copy number variation1nstd223human GRCh38 chr9: 95,447,680-95,448,706 , GRCh37.p13 chr9: 98,209,962-98,210,988 PTCH1
    nsv6443782copy number variation1nstd223human GRCh38 chr9: 95,503,733-95,504,050 , GRCh37.p13 chr9: 98,266,015-98,266,332 PTCH1
    nsv6436439copy number variation1nstd223human GRCh38 chr9: 95,505,601-95,506,300 , GRCh37.p13 chr9: 98,267,883-98,268,582 PTCH1
    nsv6436418copy number variation1nstd223human GRCh38 chr9: 95,491,532-95,492,834 , GRCh37.p13 chr9: 98,253,814-98,255,116 PTCH1
    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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