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Items: 1 to 20 of 26

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    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 CYP1B1-AS1, LOC107985771, 1649 more genes
    nsv4451022copy number variation1nstd102humanPathogenic GRCh37 chr2: 15,631,145-21,729,493 , GRCh38.p12 chr2: 15,491,021-21,506,621 RAD51AP2, LOC101928149, 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 LOC105373454, RAD51AP2, 68 more genes
    nsv3873411copy number variation1nstd102humanPathogenic GRCh37 chr2: 19,905,995-24,762,790 , GRCh38.p12 chr2: 19,706,234-24,539,921 LOC100130841, PGAM1P6, 77 more genes
    nsv6315390copy number variation1nstd102humanPathogenic GRCh37 chr2: 1-243,199,373 , GRCh38.p12 chr2: 10,001-242,157,305 LOC112268439, RNA5SP116, 3737 more genes
    nsv3874648copy number variation1nstd102humanPathogenic GRCh37 chr2: 15,672-243,101,834 , GRCh38.p12 chr2: 15,672-242,157,305 IGKV2OR2-10, LOC105374848, 3737 more genes
    nsv3885544copy number variation1nstd102humanPathogenic GRCh37 chr2: 14,238-243,048,760 , GRCh38.p12 chr2: 14,238-242,106,609 RNU6-674P, KANSL3, 3735 more genes
    nsv3882615copy number variation2nstd102humanPathogenic GRCh37 chr2: 12,771-242,783,384 , GRCh38.p12 chr2: 12,771-241,841,232 MTND2P22, LOC112268410, 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 SLC35F6, LOC105374458, 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 ALLC, LOC105373429, 674 more genes
    nsv6636815copy number variation1nstd102humanPathogenic GRCh37 chr2: 706,460-35,523,639 , GRCh38.p12 chr2: 706,460-35,298,573 LOC105374455, RN7SL674P, 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 LOC105373394, PGAM1P6, 507 more genes
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