U.S. flag

An official website of the United States government

Format
Items per page

Send to:

Choose Destination

Search results

Items: 1 to 20 of 7038

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv4871494mobile element deletion1nstd200human GRCh37 chrX: 325,371-327,135 , GRCh38.p12 chrX|NT_187634.1: 47,989-49,753 , GRCh38.p12 chrX: 364,636-366,400 , GRCh38.p12 chrX|NT_187667.1: 37,129-38,893 PPP2R3B
    nsv4787164mobile element deletion1nstd200human GRCh37 chr7: 6,380,299-6,381,374 , GRCh38.p12 chr7: 6,340,668-6,341,743 FAM220A
    nsv4907409mobile element deletion1nstd200human GRCh38 chr18: 26,247,890-26,248,838 , GRCh37.p13 chr18: 23,827,854-23,828,802 TAF4B
    nsv4899974mobile element deletion1nstd200human GRCh38 chr14: 31,326,930-31,327,576 , GRCh37.p13 chr14: 31,796,136-31,796,782 HEATR5A
    nsv4775342mobile element deletion1nstd200human GRCh37 chr14: 31,796,136-31,796,782 , GRCh38.p12 chr14: 31,326,930-31,327,576 HEATR5A
    nsv5040914mobile element deletion1nstd200human GRCh38 chrX: 1,668,671-1,669,265 , GRCh37.p13 chrX: 1,787,564-1,788,158
    nsv4907545mobile element deletion1nstd200human GRCh38 chr19: 43,477,235-43,477,823 , GRCh37.p13 chr19: 43,981,387-43,981,975 PHLDB3
    nsv4775417mobile element deletion1nstd200human GRCh37 chr19: 43,981,387-43,981,975 , GRCh38.p12 chr19: 43,477,235-43,477,823 PHLDB3
    nsv4874619mobile element deletion1nstd200human GRCh38 chr5: 134,848,415-134,848,985 , GRCh37.p13 chr5: 134,184,105-134,184,675 C5orf24
    nsv4900006mobile element deletion1nstd200human GRCh38 chr14: 55,161,408-55,161,884 , GRCh37.p13 chr14: 55,628,126-55,628,602 DLGAP5
    nsv4775384mobile element deletion1nstd200human GRCh37 chr14: 55,628,126-55,628,608 , GRCh38.p12 chr14: 55,161,408-55,161,890 DLGAP5
    nsv4893198mobile element deletion1nstd200human GRCh38 chr7: 99,213,426-99,213,889 , GRCh37.p13 chr7: 98,811,049-98,811,512 KPNA7
    nsv4882881mobile element deletion1nstd200human GRCh38 chr1: 155,827,700-155,828,154 , GRCh37.p13 chr1: 155,797,491-155,797,945 GON4L
    nsv5038329mobile element deletion1nstd200human GRCh38 chrX: 129,941,947-129,942,391 , GRCh37.p13 chrX: 129,075,923-129,076,367 LOC105373335
    nsv4887462mobile element deletion1nstd200human GRCh38 chr6: 35,420,822-35,421,264 , GRCh37.p13 chr6: 35,388,599-35,389,041 PPARD
    nsv4886479mobile element deletion1nstd200human GRCh38 chr4: 6,258,338-6,258,770 , GRCh37.p13 chr4: 6,260,065-6,260,497 WFS1
    nsv4893260mobile element deletion1nstd200human GRCh38 chr7: 157,169,694-157,170,119 , GRCh37.p13 chr7: 156,962,388-156,962,813 UBE3C
    nsv4907544mobile element deletion1nstd200human GRCh38 chr19: 42,346,300-42,346,702 , GRCh37.p13 chr19: 42,850,452-42,850,854 MEGF8
    nsv4769824mobile element deletion1nstd200human GRCh37 chr19: 42,850,452-42,850,854 , GRCh38.p12 chr19: 42,346,300-42,346,702 MEGF8
    nsv4887502mobile element deletion1nstd200human GRCh38 chr2: 127,524,876-127,525,260 , GRCh37.p13 chr2: 128,282,452-128,282,836 IWS1
    Format
    Items per page

    Send to:

    Choose Destination

    Supplemental Content

    Filters: Manage Filters

    Find related data

    Search details

    See more...

    Recent activity

    You are here: NCBI > Variation > Database of Genomic Structural Variation (dbVar)
    Support Center