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 26

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv2768204copy-neutral loss of heterozygosity1nstd125human GRCh37 chr16: 619,967-35,220,544 , GRCh38.p12 chr16: 569,967-35,986,173 ZNF764, ACSM2A, 1043 more genes
    nsv2768219copy-neutral loss of heterozygosity1nstd125human GRCh37 chr19: 260,911-20,875,551 , GRCh38.p12 chr19: 260,911-20,692,745 OR7A1P, MIR6886, 914 more genes
    nsv2768218copy-neutral loss of heterozygosity1nstd125human GRCh37 chr19: 260,911-19,856,454 , GRCh38.p12 chr19: 260,911-19,745,645 NMRK2, ELOF1, 867 more genes
    nsv2768217copy-neutral loss of heterozygosity1nstd125human GRCh37 chr19: 260,911-16,172,966 , GRCh38.p12 chr19: 260,911-16,062,156 CYP4F2, CREB3L3, 724 more genes
    nsv2768229copy-neutral loss of heterozygosity1nstd125human GRCh37 chr3: 39,873,604-53,004,620 , GRCh38.p12 chr3: 39,832,113-52,970,604 ZNF621, HYAL3, 400 more genes
    nsv2768220copy-neutral loss of heterozygosity1nstd125human GRCh37 chr19: 5,092,449-18,044,285 , GRCh38.p12 chr19: 5,092,438-17,933,476 PTPRS, ASF1B, 562 more genes
    nsv2768203copy-neutral loss of heterozygosity1nstd125human GRCh37 chr1: 47,666,145-54,633,630 , GRCh38.p12 chr1: 47,200,473-54,167,957 EPS15, SPATA6, 147 more genes
    nsv2768230copy-neutral loss of heterozygosity1nstd125human GRCh38.p12 chr3: 46,674,155-52,818,472 , GRCh37 chr3: 46,715,645-52,852,488 FCF1P2, RAD54L2, 240 more genes
    nsv2768232copy-neutral loss of heterozygosity1nstd125human GRCh38.p12 chr4: 158,719,122-164,075,078 , GRCh37 chr4: 159,640,274-164,996,230 NPY5R, LOC105379457, 35 more genes
    nsv2768216copy-neutral loss of heterozygosity1nstd125human GRCh37 chr13: 74,425,227-79,617,686 , GRCh38.p12 chr13: 73,851,090-79,043,551 SSR1P2, RNU6-38P, 72 more genes
    nsv2768214copy-neutral loss of heterozygosity1nstd125human GRCh37 chr12: 85,097,838-89,475,779 , GRCh38.p12 chr12: 84,704,059-89,082,002 RPS4XP15, LOC105369878, 38 more genes
    nsv2768205copy-neutral loss of heterozygosity1nstd125human GRCh37 chr16: 85,880-3,922,549 , GRCh38.p12 chr16: 35,880-3,872,548 E4F1, IL9RP3, 274 more genes
    nsv2768213copy-neutral loss of heterozygosity1nstd125human GRCh37 chr12: 109,772,974-113,443,181 , GRCh38.p12 chr12: 109,335,169-113,005,376 MIR6760, MIR4497, 80 more genes
    nsv2768209copy-neutral loss of heterozygosity1nstd125human GRCh37 chr1: 49,428,302-53,063,913 , GRCh38.p12 chr1: 48,962,630-52,598,241 FCF1P6, PDCL3P6, 73 more genes
    nsv2768221copy-neutral loss of heterozygosity1nstd125human GRCh37 chr5: 126,208,559-129,793,092 , GRCh38.p12 chr5: 126,872,867-130,457,399 MEGF10, MARCHF3, 39 more genes
    nsv2768215copy-neutral loss of heterozygosity1nstd125human GRCh37 chr12: 85,235,157-88,800,638 , GRCh38.p12 chr12: 84,841,378-88,406,861 LOC105369879, LINC02820, 31 more genes
    nsv2768231copy-neutral loss of heterozygosity1nstd125human GRCh38.p12 chr3: 49,698,312-53,099,510 , GRCh37 chr3: 49,735,745-53,133,526 RBM5-AS1, TEX264, 136 more genes
    nsv2768223copy-neutral loss of heterozygosity1nstd125human GRCh37 chr6: 26,097,193-29,353,408 , GRCh38.p12 chr6: 26,096,965-29,385,631 TRK-TTT3-3, H4C10P, 329 more genes
    nsv2768211copy-neutral loss of heterozygosity1nstd125human GRCh37 chr2: 38,381,205-41,553,051 , GRCh38.p12 chr2: 38,154,063-41,325,911 RNU6-373P, LOC105374497, 44 more genes
    nsv2768210copy-neutral loss of heterozygosity1nstd125human GRCh37 chr2: 134,918,553-138,074,522 , GRCh38.p12 chr2: 134,160,982-137,316,952 SMC4P1, LCT, 34 more genes
    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