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 171

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7099257copy number variation1nstd231human GRCh38.p12 chr1: 203,396,218-207,103,915 , GRCh37 chr1: 203,365,346-207,277,260 ATP2B4, AVPR1B, 116 more genes
    nsv7095955copy number variation1nstd102humanUncertain significance GRCh37 chr1: 200,522,516-206,945,780 , GRCh38.p12 chr1: 200,553,388-206,772,435 ELF3, MAPKAPK2, 189 more genes
    nsv7095569copy number variation2nstd102humanUncertain significance GRCh37 chr1: 200,522,516-208,391,267 , GRCh38.p12 chr1: 200,553,388-208,217,922 TRK-TTT8-1, ADIPOR1, 228 more genes
    nsv7054848inversion1nstd229human GRCh38 chr1: 205,678,380-205,680,901 , GRCh37.p13 chr1: 205,647,508-205,650,029 LOC105371701, SLC45A3
    nsv7044092inversion1nstd229human GRCh38 chr1: 203,118,726-211,305,271 , GRCh37.p13 chr1: 203,087,854-211,478,613 LOC100420418, LINC00260, 201 more genes
    nsv6677885copy number variation1nstd229human GRCh38 chr1: 205,629,868-205,660,717 , GRCh37.p13 chr1: 205,598,996-205,629,845 SLC45A3, ELK4
    nsv6671339copy number variation1nstd229human GRCh38 chr1: 205,662,701-205,665,900 , GRCh37.p13 chr1: 205,631,829-205,635,028 SLC45A3
    nsv6669773copy number variation1nstd229human GRCh38 chr1: 205,663,091-205,663,128 , GRCh37.p13 chr1: 205,632,219-205,632,256 SLC45A3
    nsv6636965copy number variation1nstd102humanPathogenic GRCh37 chr1: 181,453,460-213,107,248 , GRCh38.p12 chr1: 181,484,324-212,933,906 PRELP, SYT14, 527 more genes
    nsv6634372copy number variation1nstd102humanPathogenic GRCh37 chr1: 197,867,914-249,224,684 , GRCh38.p12 chr1: 197,898,784-248,930,485 LOC105373279, YBX1P9, 1036 more genes
    nsv6554773inversion1nstd223human GRCh38 chr1: 204,500,842-208,290,127 , GRCh37.p13 chr1: 204,469,970-208,463,472 RNA5SP75, LOC105372869, 108 more genes
    nsv6536401inversion1nstd223human GRCh38 chr1: 205,678,380-205,680,907 , GRCh37.p13 chr1: 205,647,508-205,650,035 LOC105371701, SLC45A3
    nsv6333678copy number variation1nstd223human GRCh38 chr1: 205,679,901-205,682,100 , GRCh37.p13 chr1: 205,649,029-205,651,228 LOC105371701, SLC45A3
    nsv6325594copy number variation1nstd223human GRCh38 chr1: 205,678,379-205,680,911 , GRCh37.p13 chr1: 205,647,507-205,650,039 SLC45A3, LOC105371701
    nsv6133967copy number variation1nstd213human GRCh37 chr1: 203,630,000-205,910,001 , GRCh38.p12 chr1: 203,660,872-205,940,873 PLEKHA6, KLHDC8A, 73 more genes
    nsv6133950copy number variation1nstd213human GRCh37 chr1: 178,070,000-205,920,001 , GRCh38.p12 chr1: 178,100,865-205,950,873 ADORA1, CACNA1E, 442 more genes
    nsv6133846copy number variation1nstd213human GRCh37 chr1: 203,140,000-205,920,001 , GRCh38.p12 chr1: 203,170,872-205,950,873 CHIT1, ELK4, 90 more genes
    nsv6133626copy number variation1nstd213human GRCh37 chr1: 205,160,000-206,320,001 , GRCh38.p12 chr1: 205,190,872-205,953,579 CDK18, LEMD1-AS1, 29 more genes
    nsv5381285copy number variation2nstd102humanUncertain significance GRCh37 chr1: 130,980,840-248,900,000 , GRCh38.p12 chr1: 120,324,463-248,736,699 , DCST1, 2428 more genes
    nsv5365086translocation1nstd200human GRCh38 chr1: 205,678,380-205,678,380 , GRCh38 chr1: 205,680,907-205,680,907 , GRCh37.p13 chr1: 205,650,035-205,650,035 , GRCh37.p13 chr1: 205,647,508-205,647,508 LOC105371701, SLC45A3
    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