U.S. flag

An official website of the United States government

Format
Items per page

Send to:

Choose Destination

Links from Gene

Items: 1 to 20 of 169

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137216copy number variation1nstd102humanPathogenic GRCh37 chr17: 30,572,862-35,843,988 , GRCh38.p12 chr17: 32,245,843-36,446,544 PSMD11, C17orf50, 117 more genes
    nsv7073998inversion1nstd229human GRCh38 chr17: 32,918,710-41,148,753 , GRCh37.p13 chr17: 31,245,728-39,305,005 LOC105371750, C17orf78, 298 more genes
    nsv7060485inversion1nstd229human GRCh38 chr17: 36,033,983-36,063,384 , GRCh37.p13 chr17: 34,361,019-34,390,744 CCL18, LOC105371746, 1 more genes
    nsv6984894copy number variation1nstd229human GRCh38 chr17: 36,062,509-36,065,148 , GRCh37.p13 chr17: 34,389,869-34,392,508 CCL18
    nsv6982390copy number variation1nstd229human GRCh38 chr17: 36,035,001-36,063,400 , GRCh37.p13 chr17: 34,362,037-34,390,760 LOC107985068, LOC105371746, 1 more genes
    nsv6624271copy number variation1nstd224human GRCh37 chr17: 34,391,721-34,819,750 , GRCh38.p12 chr17|NT_187614.1: 299,249-698,812 LOC101060212, LOC101927369, 20 more genes
    nsv6624229copy number variation1nstd224human GRCh37 chr17: 34,169,370-34,461,869 , GRCh38.p12 chr17: 35,919,249-36,134,487 , GRCh38.p12 chr17|NT_187614.1: 153,781-369,397 CCL15, CCL18, 15 more genes
    nsv6624228copy number variation1nstd224human GRCh37 chr17: 34,151,127-34,423,925 , GRCh38.p12 chr17: 35,919,249-36,096,531 , GRCh38.p12 chr17|NT_187614.1: 153,781-331,453 RDM1, LOC101927369, 11 more genes
    nsv6623848copy number variation1nstd224human GRCh37 chr17: 34,391,721-34,461,869 , GRCh38.p12 chr17: 36,064,361-36,134,487 , GRCh38.p12 chr17|NT_187661.1: 18,458-88,584 , GRCh38.p12 chr17|NT_187614.1: 299,249-369,397 CCL3, CCL4, 6 more genes
    nsv6623847copy number variation1nstd224human GRCh37 chr17: 34,291,588-34,458,934 , GRCh38.p12 chr17: 35,964,570-36,131,552 , GRCh38.p12 chr17|NT_187661.1: 1-85,649 , GRCh38.p12 chr17|NT_187614.1: 199,116-366,462 CCL14, CCL23, 13 more genes
    nsv6577423inversion1nstd223human GRCh38 chr17: 36,033,983-36,063,384 , GRCh37.p13 chr17: 34,361,019-34,390,744 CCL18, LOC105371746, 1 more genes
    nsv6510305copy number variation1nstd223human GRCh38 chr17: 35,822,938-36,193,984 , GRCh37.p13 chr17: 34,246,253-34,442,620 , LOC107985068, 26 more genes
    nsv6501005copy number variation1nstd223human GRCh38 chr17: 35,882,977-36,193,981 , GRCh37.p13 chr17: 34,246,253-34,442,620 , CCL18, 22 more genes
    nsv6499252copy number variation1nstd223human GRCh38 chr17: 36,067,901-36,070,500 , GRCh37.p13 chr17: 34,395,261-34,397,860 CCL18
    nsv5559538sequence alteration1nstd206human GRCh37.p13 chr17: 34,321,585-34,390,744 , GRCh38 chr17: 35,994,549-36,063,384 CCL15, CCL18, 4 more genes
    nsv5554090sequence alteration1nstd206human GRCh38 chr17: 32,109,732-67,925,723 , GRCh37.p13 chr17: 30,436,751-65,921,839 , APOH, 1099 more genes
    nsv5530095copy number variation1nstd206human GRCh38 chr17: 35,993,980-36,083,980 , GRCh37.p13 chr17: 34,321,016-34,411,337 CCL15, CCL18, 5 more genes
    nsv5016166copy number variation1nstd200human GRCh38 chr17: 36,068,630-36,070,115 , GRCh37.p13 chr17: 34,395,990-34,397,475 CCL18
    nsv4762422inversion1nstd199human GRCh37 chr17: 151-36,202,676 , GRCh38.p12 chr17: 150,358-36,446,544 , ABR, 1046 more genes
    nsv4684339copy number variation1nstd102humanPathogenic GRCh37 chr17: 34,360,168-36,209,228 , GRCh38 chr17|NT_187614.1: 267,696-2,088,293 , NCBI36 chr17: 31,384,281-33,283,341 TADA2A, SYNRG, 58 more genes
    Format
    Items per page

    Send to:

    Choose Destination

    Supplemental Content

    Filters: Manage Filters

    Find related data

    Recent activity

    Clear Turn Off Turn On

    Your browsing activity is empty.

    Activity recording is turned off.

    Turn recording back on

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