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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6695770copy number variation1nstd229human GRCh38 chr2: 101,102,526-102,065,468 , GRCh37.p13 chr2: 101,718,988-102,681,928 LOC107985789, PRCPP1, 17 more genes
    nsv6690397copy number variation1nstd229human GRCh38 chr2: 101,507,472-101,527,150 , GRCh37.p13 chr2: 102,123,934-102,143,612 PRCPP1, RPS6P3
    nsv6687279copy number variation1nstd229human GRCh38 chr2: 101,279,320-101,725,723 , GRCh37.p13 chr2: 101,895,782-102,342,185 MIR5696, LOC105373512, 9 more genes
    nsv6681935copy number variation1nstd229human GRCh38 chr2: 101,513,774-101,525,286 , GRCh37.p13 chr2: 102,130,236-102,141,748 PRCPP1
    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
    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
    nsv6299004copy number variation1nstd186human GRCh37 chr2: 102,019,462-102,148,080 , GRCh38.p12 chr2: 101,403,000-101,531,618 RPS6P3, RFX8, 2 more genes
    nsv6291008copy number variation1nstd102humanUncertain significance GRCh37 chr2: 101,699,537-106,383,710 , GRCh38.p12 chr2: 101,083,075-105,767,253 C2orf49, LINC01870, 71 more genes
    nsv6134605copy number variation1nstd213human GRCh37 chr2: 101,700,000-103,280,001 , GRCh38.p12 chr2: 101,083,538-102,663,542 IL1R1, SLC9A2, 27 more genes
    nsv5554214mobile element insertion1nstd206human GRCh38 chr2: 43,826,578-177,947,868 , GRCh37.p13 chr2: 44,053,717-178,812,595 , POLR1B, 2149 more genes
    nsv5446863copy number variation1nstd206human GRCh38 chr2: 101,403,000-101,531,618 , GRCh37.p13 chr2: 102,019,462-102,148,080 LINC01870, RFX8, 2 more genes
    nsv5437495copy number variation1nstd206human GRCh38 chr2: 101,513,774-101,525,286 , GRCh37.p13 chr2: 102,130,236-102,141,748 PRCPP1
    nsv5035923inversion1nstd200human GRCh38 chr2: 83,726,586-172,391,178 , GRCh37.p13 chr2: 83,953,710-173,255,906 , MTND2P21, 1427 more genes
    nsv4766632inversion1nstd199human GRCh37 chr2: 87,997,505-112,010,501 , GRCh38.p12 chr1: 125,085,511-144,884,066 , GRCh38.p12 chr2: 87,697,986-111,252,924 , GRCh38.p12 chr9: 40,649,907-63,450,751 , GRCh38.p12 chr9: 40,649,751-63,450,622 , ADRA2B, 706 more genes
    nsv4752571inversion1nstd199human GRCh37 chr2: 87,550,795-112,295,517 , GRCh38.p12 chr1: 125,085,511-144,884,066 , GRCh38.p12 chr2: 87,323,672-111,537,940 , GRCh38.p12 chr9: 40,649,907-63,450,751 , GRCh38.p12 chr9: 40,649,751-63,450,622 , ADRA2B, 723 more genes
    nsv4743379copy number variation1nstd199human GRCh37 chr2: 88,481,090-124,440,189 , GRCh38.p12 chr9: 40,649,751-63,450,622 , GRCh38.p12 chr9: 40,649,907-63,450,751 , GRCh38.p12 chr1: 125,085,511-144,884,066 , GRCh38.p12 chr2: 88,181,571-123,682,613 , EIF2AK3, 861 more genes
    nsv4312591inversion1nstd166human GRCh37.p13 chr2: 97,201,014-102,197,203 , GRCh38.p12 chr2: 96,535,277-101,580,741 , CNGA3, 106 more genes
    nsv4069270copy number variation1nstd166human GRCh37.p13 chr2: 102,130,272-102,141,748 , GRCh38.p12 chr2: 101,513,810-101,525,286 PRCPP1
    nsv3910630copy number variation1nstd102humanPathogenic NCBI36 chr2: 50,739,936-242,751,149 , GRCh37.p13 chr2: 50,886,432-243,102,476 , GRCh38.p12 chr2: 50,659,294-242,160,331 DAZAP2P1, RPL36AP16, 2991 more genes
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