U.S. flag

An official website of the United States government

Format
Items per page

Send to:

Choose Destination

Search results

Items: 19

    loading data ...

    Number of Variants: 19

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv4379109copy number variation1337nstd173human GRCh37 chr20: 1,560,774-1,597,997 , GRCh38.p12 chr20: 1,580,128-1,617,351 SIRPB1
    nsv4377460copy number variation116nstd173human GRCh37 chr16: 60,553,311-60,575,074 , GRCh38.p12 chr16: 60,519,407-60,541,170 LOC101927605
    nsv4365093copy number variation508nstd173human GRCh37 chr13: 57,758,269-57,778,379 , GRCh38.p12 chr13: 57,184,135-57,204,245 MTCO2P3
    nsv4383872copy number variation12nstd173human GRCh37 chr3: 128,380,239-128,412,365 , GRCh38.p12 chr3: 128,661,396-128,693,522 POU5F1P6
    nsv4382253copy number variation206nstd173human GRCh37 chr12: 11,503,225-11,553,849 , GRCh38.p12 chr12: 11,350,291-11,400,915 , GRCh38.p12 chr12|NT_187658.1: 545,254-572,349 PRB2, PRB1
    nsv4375232copy number variation423nstd173human GRCh37 chr5: 180,375,302-180,430,801 , GRCh38.p12 chr5: 180,948,302-181,003,801 BTNL8, LOC100128762, 3 more genes
    nsv4367271copy number variation561nstd173human GRCh37 chr11: 5,786,020-5,809,230 , GRCh38.p12 chr11: 5,764,790-5,788,000 OR56B2P, OR52N1, 1 more genes
    nsv4368821copy number variation1373nstd173human GRCh37 chr22: 24,353,749-24,385,040 , GRCh38.p12 chr22|NT_187633.1: 247,924-279,215 LOC391322, GSTTP2, 3 more genes
    nsv4371991copy number variation196nstd173human GRCh37 chr19: 20,596,118-20,720,705 , GRCh38.p12 chr19: 20,413,312-20,537,899 ZNF826P, ZNF737, 4 more genes
    nsv4380971copy number variation213nstd173human GRCh37 chr6: 29,841,021-29,936,041 , GRCh38.p12 chr6: 29,873,244-29,968,264 HLA-H, HCG4P4, 12 more genes
    nsv4370779copy number variation156nstd173human GRCh37 chr5: 8,702,522-8,750,244 , GRCh38.p12 chr5: 8,702,410-8,750,132 0
    nsv4378128copy number variation463nstd173human GRCh37 chr11: 51,337,076-51,376,963 , GRCh38.p12 chr11: 54,742,317-54,782,204 0
    nsv4374063copy number variation2nstd173human GRCh37 chrX: 149,190,831-149,229,329 , GRCh38.p12 chrX: 150,022,600-150,061,098 0
    nsv4373392copy number variation11nstd173human GRCh37 chr2: 35,581,997-35,611,032 , GRCh38.p12 chr2: 35,356,931-35,385,966 0
    nsv4375754copy number variation4nstd173human GRCh37 chr6: 31,280,867-31,305,298 , GRCh38.p12 chr6: 31,313,090-31,337,521 0
    nsv4379470copy number variation1nstd173human GRCh37 chr14: 22,505,307-22,959,418 , GRCh38.p12 chr14: 22,037,065-22,490,430 TRAJ55, TRAV28, 54 more genes
    nsv4378873copy number variation1nstd173human GRCh37 chr14: 106,872,841-106,952,842 , GRCh38.p12 chr14: 106,416,924-106,496,828 , GRCh38.p12 chr14|NT_187600.1: 908,603-988,507 IGHV3-42, IGHV7-40, 12 more genes
    nsv4377353copy number variation2nstd173human GRCh37 chr6: 103,759,824-103,810,717 , GRCh38.p12 chr6: 103,311,949-103,362,842 0
    nsv4368473copy number variation289nstd173human GRCh37 chr22: 42,918,351-42,943,641 , GRCh38.p12 chr22: 42,522,345-42,547,635 0
    Format
    Items per page

    Send to:

    Choose Destination

    Supplemental Content

    Filters: Manage Filters

    Find related data

    Search details

    See more...

    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