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 530

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6635140copy number variation12nstd227human GRCh37 chr16: 28,615,243-28,620,752 , GRCh38.p12 chr16: 28,603,922-28,609,431 SULT1A1
    nsv6635875copy number variation5nstd227human GRCh37 chr15: 32,509,892-32,514,341 , GRCh38.p12 chr15: 32,217,691-32,222,140 LOC102724078
    nsv6634788copy number variation1nstd227human GRCh38.p12 chr8: 138,768,766-139,478,689 , GRCh37 chr8: 139,781,009-140,490,932 COL22A1
    nsv6634767copy number variation1nstd227human GRCh38.p12 chr4: 115,242,871-115,690,953 , GRCh37 chr4: 116,164,027-116,612,109 RPF2P2
    nsv6635269copy number variation1nstd227human GRCh37 chr7: 62,113,011-62,479,327 , GRCh38.p12 chr7: 62,652,633-63,018,949 RNU6-417P
    nsv6635614copy number variation1nstd227human GRCh38.p12 chr1: 175,459,821-175,766,244 , GRCh37 chr1: 175,428,957-175,735,380 TNR
    nsv6635472copy number variation1nstd227human GRCh38.p12 chr21: 40,919,752-41,146,107 , GRCh37 chr21: 42,291,678-42,518,034 LINC00323
    nsv6635326copy number variation1nstd227human GRCh37 chr7: 100,968,363-101,138,286 , GRCh38.p12 chr7: 101,325,082-101,495,005 COL26A1
    nsv6635916copy number variation3nstd227human GRCh38.p12 chr9: 135,257,320-135,406,318 , GRCh37 chr9: 138,149,166-138,298,164 LINC02907
    nsv6635179copy number variation1nstd227human GRCh38.p12 chr9: 135,257,320-135,400,692 , GRCh37 chr9: 138,149,166-138,292,538 LINC02907
    nsv6634747copy number variation1nstd227human GRCh37 chr3: 162,088,699-162,216,666 , GRCh38.p12 chr3: 162,370,911-162,498,878 TOMM22P6
    nsv6635238copy number variation1nstd227human GRCh38.p12 chr6: 67,823,072-67,921,586 , GRCh37 chr6: 68,532,965-68,631,478 LOC105377845
    nsv6634910copy number variation1nstd227human GRCh37 chr5: 101,001,326-101,096,015 , GRCh38.p12 chr5: 101,665,622-101,760,311 LOC105379102
    nsv6635330copy number variation1nstd227human GRCh38.p12 chr14: 62,534,442-62,627,689 , GRCh37 chr14: 63,001,160-63,094,407 ATP5F1AP4
    nsv6635319copy number variation1nstd227human GRCh38.p12 chr14: 44,355,671-44,446,152 , GRCh37 chr14: 44,824,874-44,915,355 LINC02277
    nsv6635964copy number variation1nstd227human GRCh38.p12 chr10: 116,316,286-116,400,120 , GRCh37 chr10: 118,075,798-118,159,632 CCDC172
    nsv6635233copy number variation1nstd227human GRCh37 chr18: 64,791,559-64,874,851 , GRCh38.p12 chr18: 67,124,322-67,207,614 RPL31P9
    nsv6634987copy number variation1nstd227human GRCh38.p12 chr13: 111,020,469-111,103,066 , GRCh37 chr13: 111,672,816-111,755,413 LINC00368
    nsv6634943copy number variation1nstd227human GRCh38.p12 chr10: 115,464,095-115,545,746 , GRCh37 chr10: 117,223,605-117,305,256 ATRNL1
    nsv6635862copy number variation1nstd227human GRCh37 chr3: 173,233,354-173,310,353 , GRCh38.p12 chr3: 173,515,564-173,592,563 NLGN1
    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