U.S. flag

An official website of the United States government

Format
Items per page

Send to:

Choose Destination

Links from BioSystems

Items: 1 to 20 of 34211

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6137806copy number variation1nstd102humanUncertain significance GRCh37 chr3: 196,539,700-196,612,739 , GRCh38.p12 chr3: 196,812,829-196,885,868 SENP5, PAK2
    nsv6137736copy number variation1nstd102humanPathogenic GRCh37 chrX: 153,263,517-155,260,560 , GRCh38.p12 chrX: 153,998,066-156,030,895 H2AB3, GDI1, 83 more genes
    nsv6137727copy number variation2nstd102humanUncertain significance GRCh38 chr3: 12,589,035-12,766,981 , GRCh37.p13 chr3: 12,630,534-12,808,480 RAF1, CRIP1P1, 1 more genes
    nsv6137666copy number variation1nstd102humanPathogenic GRCh37 chrX: 91,829,757-113,050,225 , GRCh38.p12 chrX: 92,574,758-113,806,943 TCEAL8, MTND5P26, 272 more genes
    nsv6131704insertion1nstd186human GRCh37 chr18: 77,224,671-77,224,680 , GRCh38.p12 chr18: 79,464,671-79,464,680 NFATC1, LOC101927897
    nsv6131193insertion1nstd186human GRCh37 chr18: 77,160,842-77,160,883 , GRCh38.p12 chr18: 79,400,842-79,400,883 NFATC1
    nsv6130735insertion1nstd186human GRCh37 chr16: 68,126,512-68,126,512 , GRCh38.p12 chr16: 68,092,609-68,092,609 NFATC3
    nsv6130204insertion1nstd186human GRCh37 chr18: 77,241,814-77,241,832 , GRCh38.p12 chr18: 79,481,814-79,481,832 NFATC1
    nsv6130114insertion1nstd186human GRCh37 chr18: 77,227,360-77,227,385 , GRCh38.p12 chr18: 79,467,360-79,467,385 NFATC1, LOC101927897, 1 more genes
    nsv6129932insertion1nstd186human GRCh37 chr17: 43,339,871-43,339,878 , GRCh38.p12 chr17: 45,262,504-45,262,511 MAP3K14, SPATA32, 1 more genes
    nsv6129266insertion1nstd186human GRCh37 chr20: 50,024,987-50,024,987 , GRCh38.p12 chr20: 51,408,450-51,408,450 NFATC2
    nsv6129263insertion1nstd186human GRCh37 chr19: 10,447,948-10,447,948 , GRCh38.p12 chr19: 10,337,272-10,337,272 ICAM3
    nsv6126741copy number variation1nstd186human GRCh37 chr22: 39,819,771-39,819,994 , GRCh38.p12 chr22: 39,423,766-39,423,989 TAB1
    nsv6125658copy number variation1nstd186human GRCh37 chr19: 9,015,192-9,017,985 , GRCh38.p12 chr19: 8,904,516-8,907,309 MUC16
    nsv6125378insertion1nstd186human GRCh37 chr12: 26,650,425-26,650,472 , GRCh38.p12 chr12: 26,497,492-26,497,539 ITPR2
    nsv6123537copy number variation1nstd186human GRCh37 chr18: 77,168,906-77,169,228 , GRCh38.p12 chr18: 79,408,906-79,409,228 NFATC1
    nsv6123439copy number variation1nstd186human GRCh37 chr19: 539,824-540,779 , GRCh38.p12 chr19: 539,824-540,779 CDC34
    nsv6123429copy number variation1nstd186human GRCh37 chr18: 23,762,725-23,766,215 , GRCh38.p12 chr18: 26,182,761-26,186,251 PSMA8
    nsv6122526copy number variation1nstd186human GRCh37 chr7: 100,678,416-100,679,747 , GRCh38.p12 chr7: 101,035,135-101,036,466 MUC17
    nsv6118437copy number variation1nstd186human GRCh37 chr3: 195,507,694-195,510,211 , GRCh38.p12 chr3: 195,780,823-195,783,340 , GRCh38.p12 chr3|NT_187688.1: 11,396-13,913 , GRCh38.p12 chr3|NT_187691.1: 11,396-13,913 , GRCh38.p12 chr3|NT_187678.1: 11,396-13,916 , GRCh38.p12 chr3|NT_187689.1: 150,602-153,125 , GRCh38.p12 chr3|NT_187690.1: 11,396-13,913 , GRCh38.p12 chr3|NT_187649.1: 11,396-13,913 MUC4
    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