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 211

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7144729insertion1nstd232human GRCh37.p13 chr3: 197,849,225-197,849,225 , GRCh38.p12 chr3: 198,122,354-198,122,354 , GRCh38.p12 chr3|NT_187539.1: 113,264-113,264 TUBB8P8
    nsv7057387inversion1nstd229human GRCh38 chr3: 198,049,771-198,124,769 , GRCh37.p13 chr3: 197,776,642-197,851,640 TUBB8P8, FRG2FP, 2 more genes
    nsv6730819copy number variation1nstd229human GRCh38 chr3: 198,016,699-198,169,505 , GRCh37.p13 chr3: 197,743,570-197,896,376 FRG2FP, LMLN-AS1, 5 more genes
    nsv6634371copy number variation1nstd102humanLikely pathogenic GRCh37 chr3: 171,549,421-198,022,430 , GRCh38.p12 chr3: 171,831,631-198,235,559 ACTL6A, AHSG, 466 more genes
    nsv6628751copy number variation1nstd224human GRCh37 chr3: 197,716,313-197,871,052 , GRCh38.p12 chr3: 197,989,442-198,144,181 , GRCh38.p12 chr3|NT_187539.1: 91,379-184,404 LMLN, ANKRD18DP, 5 more genes
    nsv6315437copy number variation1nstd102humanPathogenic GRCh37 chr3: 183,498,520-197,851,986 , GRCh38.p12 chr3: 183,780,732-198,125,115 LOC105374291, GP5, 315 more genes
    nsv6291411copy number variation1nstd102humanUncertain significance GRCh37 chr3: 195,993,691-197,851,986 , GRCh38.p12 chr3: 196,266,820-198,125,115 IQCG, PAK2, 62 more genes
    nsv6290249copy number variation1nstd102humanUncertain significance GRCh37 chr3: 194,790,394-197,961,930 , GRCh38.p12 chr3: 195,069,665-198,235,059 FRG2FP, LOC105374308, 107 more genes
    nsv6134801copy number variation1nstd213human GRCh37 chr3: 196,820,000-197,940,001 , GRCh38.p12 chr3: 197,093,129-198,213,130 ANKRD18DP, MIR922, 28 more genes
    nsv5993140copy number variation1nstd212human GRCh38 chr3: 198,117,058-198,123,296 , GRCh37.p13 chr3: 197,843,929-197,850,167 TUBB8P8
    nsv5895409copy number variation1nstd209human GRCh38 chr3: 198,117,055-198,123,294 , GRCh37.p13 chr3: 197,843,926-197,850,165 TUBB8P8
    nsv5835822copy number variation2nstd209human GRCh38 chr3: 198,117,445-198,118,494 , GRCh37.p13 chr3: 197,844,316-197,845,365 TUBB8P8
    nsv5835212copy number variation2nstd209human GRCh38 chr3: 198,119,295-198,123,269 , GRCh37.p13 chr3: 197,846,166-197,850,140 TUBB8P8
    nsv5572151copy number variation1nstd207human GRCh38 chr3: 198,117,055-198,123,294 , GRCh37.p13 chr3: 197,843,926-197,850,165 TUBB8P8
    nsv5453639copy number variation1nstd206human GRCh38 chr3: 163,047,000-198,226,000 , GRCh37.p13 chr3: 162,764,788-197,952,871 , MIR922, 587 more genes
    nsv5452043copy number variation1nstd206human GRCh38 chr3: 198,117,038-198,123,315 , GRCh37.p13 chr3: 197,843,909-197,850,186 TUBB8P8
    nsv5319321copy number variation1nstd204human GRCh38.p13 chr3: 198,117,058-198,123,295 , GRCh37.p13 chr3: 197,843,929-197,850,166 TUBB8P8
    nsv5305854copy number variation1nstd204human GRCh38.p13 chr3: 198,082,102-198,171,681 , GRCh37.p13 chr3: 197,808,973-197,898,552 , FRG2FP, 2 more genes
    nsv5239670copy number variation1nstd204human GRCh38.p13 chr3: 198,120,330-198,123,294 , GRCh37.p13 chr3: 197,847,201-197,850,165 TUBB8P8
    nsv5234874copy number variation1nstd204human GRCh38.p13 chr3: 198,105,801-198,141,400 , GRCh37.p13 chr3: 197,832,672-197,868,271 FRG2FP, TUBB8P8
    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