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 351

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148054copy number variation1nstd102humanPathogenic GRCh37 chr1: 142,535,935-157,648,813 , GRCh38.p12 chr1: 120,175,847-149,601,750 , TRN-GTT12-1, 266 more genes
    nsv7056211inversion1nstd229human GRCh38 chr1: 143,881,700-152,159,818 , GRCh37.p13 chr1|NW_003871055.3: 697,113-7,283,150 , PDIA3P1, 333 more genes
    nsv6634349copy number variation1nstd102humanPathogenic GRCh37 chr1: 145,157,447-148,016,122 , GRCh38.p12 chr1: 144,536,526-149,492,442 , TRN-GTT10-1, 170 more genes
    nsv6138373copy number variation1nstd206human GRCh38 chr1: 149,488,587-149,534,587 , GRCh37.p13 chr1|NW_003871055.3: 6,304,000-6,350,000 NBPF19
    nsv6138150copy number variation1nstd206human GRCh38 chr1: 149,536,587-149,552,587 , GRCh37.p13 chr1|NW_003871055.3: 6,352,000-6,368,000 NBPF19
    nsv5981597copy number variation1nstd212human GRCh38 chr1: 149,501,555-149,501,610 , GRCh37.p13 chr1|NW_003871055.3: 6,316,968-6,317,023 NBPF19
    nsv5981207copy number variation1nstd212human GRCh38 chr1: 149,539,573-149,539,630 , GRCh37.p13 chr1: 148,267,059-148,267,116 , GRCh37.p13 chr1|NW_003871055.3: 6,354,986-6,355,043 NBPF19
    nsv5981124copy number variation1nstd212human GRCh38 chr1: 149,530,071-149,530,129 , GRCh37.p13 chr1: 148,276,596-148,276,654 , GRCh37.p13 chr1|NW_003871055.3: 6,345,484-6,345,542 NBPF19
    nsv5624326insertion1nstd207human GRCh38 chr1: 149,550,679-149,550,679 , GRCh37.p13 chr1|NW_003871055.3: 6,366,092-6,366,092 NBPF19
    nsv5619443insertion1nstd207human GRCh38 chr1: 149,545,740-149,545,740 , GRCh37.p13 chr1|NW_003871055.3: 6,361,153-6,361,153 NBPF19
    nsv5618510insertion1nstd207human GRCh38 chr1: 149,517,923-149,517,923 , GRCh37.p13 chr1|NW_003871055.3: 6,333,336-6,333,336 NBPF19
    nsv5583295copy number variation1nstd207human GRCh38 chr1: 149,530,072-149,530,129 , GRCh37.p13 chr1|NW_003871055.3: 6,345,485-6,345,542 , GRCh37.p13 chr1: 148,276,596-148,276,653 NBPF19
    nsv5422355copy number variation1nstd206human GRCh37.p13 chr1|NW_003871055.3: 6,178,000-6,401,206 , GRCh38 chr1: 149,362,587-149,585,793 PPIAL4C, SEC22B2P, 5 more genes
    nsv5421148copy number variation1nstd206human GRCh37.p13 chr1|NW_003871055.3: 6,178,000-6,361,206 , GRCh38 chr1: 149,362,587-149,545,793 LOC105371403, NOTCH2NLC, 2 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
    nsv5220129copy number variation1nstd204human GRCh38.p13 chr1: 149,498,001-149,511,100 , GRCh37.p13 chr1|NW_003871055.3: 6,313,414-6,326,513 NBPF19
    nsv5220028copy number variation1nstd204human GRCh38.p13 chr1: 149,513,301-149,523,300 , GRCh37.p13 chr1|NW_003871055.3: 6,328,714-6,338,713 NBPF19
    nsv5219762copy number variation1nstd204human GRCh38.p13 chr1: 149,508,501-149,521,100 , GRCh37.p13 chr1|NW_003871055.3: 6,323,914-6,336,513 NBPF19
    nsv5218866copy number variation1nstd204human GRCh38.p13 chr1: 149,533,801-149,538,900 , GRCh37.p13 chr1|NW_003871055.3: 6,349,214-6,354,313 , GRCh37.p13 chr1: 148,267,789-148,272,911 NBPF19
    nsv5218775copy number variation1nstd204human GRCh38.p13 chr1: 149,499,501-149,502,600 , GRCh37.p13 chr1|NW_003871055.3: 6,314,914-6,318,013 NBPF19
    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