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 514

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3170181copy number variation6nstd156human NCBI36 chr1: 187,559,417-187,813,593 , GRCh37.p13 chr1: 189,292,794-189,546,970 , GRCh38.p12 chr1: 189,323,664-189,577,840 LOC105371657
    nsv3170123copy number variation3nstd156human NCBI36 chr16: 18,585,612-18,698,609 , GRCh37.p13 chr16: 18,678,111-18,791,108 , GRCh38.p12 chr16: 18,666,789-18,779,786 RPS15A
    nsv3169661copy number variation10nstd156human NCBI36 chr11: 54,696,918-54,795,833 , GRCh37.p13 chr11: 54,940,342-55,039,257 , GRCh38.p12 chr11: 55,172,866-55,271,781 TRIM48
    nsv3169798copy number variation2nstd156human NCBI36 chr9: 127,910,655-128,005,930 , GRCh37.p13 chr9: 128,870,834-128,966,109 , GRCh38.p12 chr9: 126,108,555-126,203,830 LOC105376274
    nsv3169872copy number variation59nstd156human NCBI36 chr7: 64,206,287-64,274,563 , GRCh37.p13 chr7: 64,568,852-64,637,128 , GRCh38.p12 chr7: 65,108,474-65,176,750 INTS4P1
    nsv3169899copy number variation53nstd156human NCBI36 chr2: 97,484,644-97,528,621 , GRCh37.p13 chr2: 97,893,136-97,921,197 , GRCh38.p12 chr2: 97,501,749-97,545,726 ANKRD36B
    nsv3169883copy number variation2nstd156human NCBI36 chr5: 97,096,711-97,125,076 , GRCh37.p13 chr5: 97,070,955-97,099,320 , GRCh38.p12 chr5: 97,735,251-97,763,616 LOC391813
    nsv3169751copy number variation21nstd156human NCBI36 chr6: 81,331,055-81,355,772 , GRCh37.p13 chr6: 81,274,336-81,299,053 , GRCh38.p12 chr6: 80,564,619-80,589,336 LOC112267962
    nsv3169739copy number variation26nstd156human NCBI36 chr7: 149,916,037-149,938,855 , GRCh37.p13 chr7: 150,285,104-150,307,922 , GRCh38.p12 chr7: 150,588,016-150,610,834 EIF2AP2
    nsv3169465copy number variation5nstd156human NCBI36 chr1: 34,864,261-34,886,855 , GRCh37.p13 chr1: 35,091,674-35,114,268 , GRCh38.p12 chr1: 34,626,073-34,648,667 LOC105378641
    nsv3170200copy number variation41nstd156human NCBI36 chr2: 179,769,900-179,791,836 , GRCh37.p13 chr2: 180,061,655-180,083,591 , GRCh38.p12 chr2: 179,196,928-179,218,864 SESTD1
    nsv3170079copy number variation2nstd156human NCBI36 chr4: 53,761,762-53,781,496 , GRCh37.p13 chr4: 54,067,005-54,086,739 , GRCh38.p12 chr4: 53,200,838-53,220,572 SCFD2
    nsv3170130copy number variation15nstd156human NCBI36 chr18: 64,890,114-64,909,563 , GRCh37.p13 chr18: 66,739,134-66,758,583 , GRCh38.p12 chr18: 69,071,897-69,091,346 CCDC102B
    nsv3170159copy number variation3nstd156human NCBI36 chr3: 17,504,549-17,521,442 , GRCh37.p13 chr3: 17,529,545-17,546,438 , GRCh38.p12 chr3: 17,488,053-17,504,946 TBC1D5
    nsv3169620copy number variation24nstd156human NCBI36 chr10: 56,350,283-56,365,424 , GRCh37.p13 chr10: 56,680,277-56,695,418 , GRCh38.p12 chr10: 54,920,517-54,935,658 PCDH15
    nsv3169611copy number variation13nstd156human NCBI36 chr8: 3,764,272-3,778,626 , GRCh37.p13 chr8: 3,776,864-3,791,218 , GRCh38.p12 chr8: 3,919,342-3,933,696 CSMD1
    nsv3169639copy number variation20nstd156human NCBI36 chr7: 157,030,238-157,044,516 , GRCh37.p13 chr7: 157,337,477-157,351,755 , GRCh38.p12 chr7: 157,544,783-157,559,061 PTPRN2
    nsv3170257copy number variation20nstd156human NCBI36 chr7: 133,435,717-133,449,712 , GRCh37.p13 chr7: 133,785,177-133,799,172 , GRCh38.p12 chr7: 134,100,424-134,114,419
    nsv3170267copy number variation15nstd156human NCBI36 chr19: 9,134,800-9,145,760 , GRCh37.p13 chr19: 9,273,800-9,284,760 , GRCh38.p12 chr19: 9,163,124-9,174,084 ZNF317
    nsv3170234copy number variation13nstd156human NCBI36 chr9: 28,034,704-28,045,603 , GRCh37.p13 chr9: 28,044,704-28,055,603 , GRCh38.p12 chr9: 28,044,706-28,055,605 LINGO2
    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