U.S. flag

An official website of the United States government

Format
Items per page

Send to:

Choose Destination

Search results

Items: 1 to 20 of 26

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3875930copy number variation1nstd102humanBenign GRCh37 chr2: 20,421,008-20,430,049 , GRCh38.p12 chr2: 20,221,247-20,230,288 SDC1
    nsv3878790copy number variation1nstd102humanBenign GRCh37 chr2: 20,423,867-20,427,189 , GRCh38.p12 chr2: 20,224,106-20,227,428 SDC1
    nsv3871744copy number variation1nstd102humanBenign GRCh37 chr2: 20,423,264-20,425,165 , GRCh38.p12 chr2: 20,223,503-20,225,404 SDC1
    nsv3875111copy number variation1nstd102humanBenign GRCh37 chr2: 20,423,601-20,425,165 , GRCh38.p12 chr2: 20,223,840-20,225,404 SDC1
    nsv3886729copy number variation1nstd102humanBenign GRCh37 chr2: 20,423,488-20,424,838 , GRCh38.p12 chr2: 20,223,727-20,225,077 SDC1
    nsv3884237copy number variation1nstd102humanBenign GRCh37 chr2: 20,423,601-20,424,838 , GRCh38.p12 chr2: 20,223,840-20,225,077 SDC1
    nsv3878056copy number variation1nstd102humanBenign GRCh37 chr2: 20,423,488-20,424,725 , GRCh38.p12 chr2: 20,223,727-20,224,964 SDC1
    nsv3888344copy number variation1nstd102humanBenign GRCh37 chr2: 20,423,601-20,424,725 , GRCh38.p12 chr2: 20,223,840-20,224,964 SDC1
    nsv6634330copy number variation1nstd102humanPathogenic GRCh37 chr2: 11,504,318-111,365,996 , GRCh38.p12 chr2: 11,364,192-110,608,419 SDC1, CYP1B1-AS1, 1649 more genes
    nsv4451022copy number variation1nstd102humanPathogenic GRCh37 chr2: 15,631,145-21,729,493 , GRCh38.p12 chr2: 15,491,021-21,506,621 SDC1, RAD51AP2, 82 more genes
    nsv3891917copy number variation1nstd102humanPathogenic GRCh37 chr2: 16,904,863-21,823,606 , GRCh38 chr2: 16,723,596-21,600,734 , NCBI36 chr2: 16,768,344-21,677,111 SDC1, LOC105373454, 68 more genes
    nsv3873411copy number variation1nstd102humanPathogenic GRCh37 chr2: 19,905,995-24,762,790 , GRCh38.p12 chr2: 19,706,234-24,539,921 SDC1, LOC100130841, 77 more genes
    nsv6315390copy number variation1nstd102humanPathogenic GRCh37 chr2: 1-243,199,373 , GRCh38.p12 chr2: 10,001-242,157,305 SDC1, LOC112268439, 3737 more genes
    nsv3874648copy number variation1nstd102humanPathogenic GRCh37 chr2: 15,672-243,101,834 , GRCh38.p12 chr2: 15,672-242,157,305 SDC1, IGKV2OR2-10, 3737 more genes
    nsv3885544copy number variation1nstd102humanPathogenic GRCh37 chr2: 14,238-243,048,760 , GRCh38.p12 chr2: 14,238-242,106,609 SDC1, RNU6-674P, 3735 more genes
    nsv3882615copy number variation2nstd102humanPathogenic GRCh37 chr2: 12,771-242,783,384 , GRCh38.p12 chr2: 12,771-241,841,232 SDC1, MTND2P22, 3724 more genes
    nsv3908605copy number variation1nstd102humanPathogenic GRCh37 chr2: 66,097-55,797,773 , GRCh38 chr2: 66,097-55,570,637 , NCBI36 chr2: 56,097-55,651,277 SDC1, SLC35F6, 801 more genes
    nsv3908288copy number variation1nstd102humanPathogenic GRCh37 chr2: 236,816-46,210,371 , GRCh38 chr2: 236,816-45,983,232 , NCBI36 chr2: 226,816-46,063,875 SDC1, ALLC, 674 more genes
    nsv6636815copy number variation1nstd102humanPathogenic GRCh37 chr2: 706,460-35,523,639 , GRCh38.p12 chr2: 706,460-35,298,573 SDC1, LOC105374455, 504 more genes
    nsv3908038copy number variation1nstd102humanPathogenic GRCh37 chr2: 12,770-33,936,576 , NCBI36 chr2: 2,770-33,790,080 , GRCh38 chr2: 12,770-33,711,509 SDC1, LOC105373394, 507 more genes
    Format
    Items per page

    Send to:

    Choose Destination

    Supplemental Content

    Filters: Manage Filters

    Find related data

    Search details

    See more...

    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