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 185

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7049205inversion1nstd229human GRCh38 chr2: 88,027,579-88,250,627 , GRCh37.p13 chr2: 88,327,098-88,550,146 MIR4780, FABP1, 5 more genes
    nsv7038954inversion1nstd229human GRCh38 chr2: 87,830,296-88,131,844 , GRCh37.p13 chr2: 88,129,815-88,431,363 ANAPC1P5, SMYD1, 9 more genes
    nsv6693211copy number variation1nstd229human GRCh38 chr2: 88,012,301-88,029,100 , GRCh37.p13 chr2: 88,311,820-88,328,619 LOC105374852, RNU2-63P, 1 more genes
    nsv6691669copy number variation1nstd229human GRCh38 chr2: 87,425,578-90,288,757 , GRCh37.p13 chr2: 87,652,701-90,295,274 LOC105374854, IGKV1-22, 130 more genes
    nsv6691650copy number variation1nstd229human GRCh38 chr2: 88,049,610-88,051,036 , GRCh37.p13 chr2: 88,349,129-88,350,555 KRCC1
    nsv6684553copy number variation1nstd229human GRCh38 chr2: 88,011,926-88,026,552 , GRCh37.p13 chr2: 88,311,445-88,326,071 LOC105374852, RNU2-63P, 1 more genes
    nsv6684214copy number variation1nstd229human GRCh38 chr2: 88,042,001-88,079,900 , GRCh37.p13 chr2: 88,341,520-88,379,419 KRCC1, SMYD1
    nsv6636373copy number variation1nstd102humanUncertain significance GRCh37 chr2: 88,046,609-89,126,291 , GRCh38.p12 chr2: 87,747,090-88,826,778 THNSL2, SMYD1, 31 more genes
    nsv6634330copy number variation1nstd102humanPathogenic GRCh37 chr2: 11,504,318-111,365,996 , GRCh38.p12 chr2: 11,364,192-110,608,419 CYP1B1-AS1, LOC107985771, 1649 more genes
    nsv6342097copy number variation1nstd223human GRCh38 chr2: 88,011,926-88,026,552 , GRCh37.p13 chr2: 88,311,445-88,326,071 RNU2-63P, KRCC1, 1 more genes
    nsv6339361copy number variation1nstd223human GRCh38 chr2: 88,012,321-88,029,118 , GRCh37.p13 chr2: 88,311,840-88,328,637 RNU2-63P, LOC105374852, 1 more genes
    nsv6315390copy number variation1nstd102humanPathogenic GRCh37 chr2: 1-243,199,373 , GRCh38.p12 chr2: 10,001-242,157,305 LOC112268439, RNA5SP116, 3737 more genes
    nsv6314726copy number variation1nstd102humanLikely pathogenic GRCh37 chr2: 40,607,042-146,902,764 , GRCh38.p12 chr2: 40,379,902-146,145,196 ACTG2, ACYP2, 1713 more genes
    nsv6252722mobile element insertion1nstd215human GRCh38 chr2: 88,054,989-88,054,989 , GRCh37.p13 chr2: 88,354,508-88,354,508 KRCC1
    nsv6157992copy number variation1nstd214human GRCh38 chr2: 88,052,496-88,052,561 , GRCh37.p13 chr2: 88,352,015-88,352,080 KRCC1
    nsv6112673copy number variation1nstd102humanPathogenic GRCh37 chr2: 88,007,281-90,260,248 , GRCh38.p12 chr2: 87,707,762-90,221,382 IGKV3-20, IGKV3-7, 122 more genes
    nsv5990217copy number variation1nstd212human GRCh38 chr2: 88,052,496-88,052,562 , GRCh37.p13 chr2: 88,352,015-88,352,081 KRCC1
    nsv5878164copy number variation1nstd209human GRCh38 chr2: 88,052,496-88,052,561 , GRCh37.p13 chr2: 88,352,015-88,352,080 KRCC1
    nsv5727120mobile element insertion1nstd211human GRCh38 chr2: 88,051,108-88,051,108 , GRCh37.p13 chr2: 88,350,627-88,350,627 KRCC1
    nsv5575187copy number variation1nstd207human GRCh38 chr2: 88,052,496-88,052,561 , GRCh37.p13 chr2: 88,352,015-88,352,080 KRCC1
    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