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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv4579247copy number variation1nstd183human GRCh37 chr1: 143,344,621-143,419,637 , GRCh38.p12 chr14|NT_113796.3: 1,805-76,821 ANKRD20A15P, LOC105379271, 2 more genes
    nsv4578987copy number variation1nstd183human GRCh37 chr1: 143,345,593-143,417,129 , GRCh38.p12 chr14|NT_113796.3: 2,777-74,313 LOC105379272, SNX18P20, 2 more genes
    nsv4405611copy number variation1nstd174human GRCh37 chr1: 143,344,215-143,500,200 , GRCh38.p12 chr14|NT_113796.3: 1,399-157,384 SNX18P20, LOC105379271, 3 more genes
    nsv4396268copy number variation1nstd174human GRCh37 chr1: 143,343,508-143,419,637 , GRCh38.p12 chr14|NT_113796.3: 692-76,821 ANKRD20A15P, LOC105379271, 2 more genes
    nsv3922074copy number variation1nstd102humanUncertain significance NCBI36 chr1: 142,122,919-142,349,638 , GRCh37.p13 chr1: 143,281,396-143,508,115 , GRCh38.p12 chr14|NT_113796.3: 2-165,299 LOC105379272, SNX18P20, 3 more genes
    nsv3358491copy number variation12nstd162human GRCh38 chr14|NT_113796.3: 9,101-70,200 , GRCh37.p13 chr1: 143,351,917-143,413,016 SNX18P20, ANKRD20A15P, 2 more genes
    nsv3344805copy number variation5nstd162human GRCh38 chr14|NT_113796.3: 15,501-36,100 , GRCh37.p13 chr1: 143,358,317-143,378,916 ANKRD20A15P
    nsv2762285copy number variation1nstd130human GRCh37 chr1: 143,281,481-143,531,627 , GRCh38.p12 chr14|NT_113796.3: 2-188,811 ANKRD20A15P, LOC105379271, 3 more genes
    nsv2759303copy number variation1nstd130human GRCh37 chr1: 143,272,542-143,544,285 , GRCh38.p12 chr14|NT_113796.3: 2-201,469 LOC105379272, ANKRD20A15P, 3 more genes
    nsv2753799copy number variation1nstd130human GRCh37 chr1: 143,245,684-143,544,285 , GRCh38.p12 chr14|NT_113796.3: 2-201,469 LOC105379271, SNX18P22, 3 more genes
    nsv1172910copy number variation171nstd112Neandertal, Denisova hominin, human GRCh37 chr1: 143,343,095-143,544,442 , GRCh38.p12 chr14|NT_113796.3: 279-201,626 SNX18P20, LOC105379271, 3 more genes
    nsv1147243copy number variation1nstd107human GRCh37 chr1: 143,342,999-143,544,500 , GRCh38.p12 chr14|NT_113796.3: 183-201,684 SNX18P20, SNX18P22, 3 more genes
    nsv1139495copy number variation1nstd106human GRCh37 chr1: 143,343,100-143,442,800 , GRCh38.p12 chr14|NT_113796.3: 284-99,984 SNX18P20, SNX18P22, 3 more genes
    nsv1128607copy number variation1nstd106human GRCh37 chr1: 143,343,000-143,383,300 , GRCh38.p12 chr14|NT_113796.3: 184-40,484 ANKRD20A15P, LOC105379271
    nsv1077295copy number variation1nstd99human GRCh37 chr1: 143,357,499-143,432,800 , GRCh38.p12 chr14|NT_113796.3: 14,683-89,984 SNX18P20, SNX18P22, 3 more genes
    esv3451964copy number variation1estd59human NCBI36 chr1: 142,183,352-142,219,250 , GRCh37.p13 chr1: 143,341,829-143,377,727 , GRCh38.p12 chr14|NT_113796.3: 1-34,911 ANKRD20A15P
    esv3408833copy number variation1estd59human NCBI36 chr1: 142,217,952-142,226,050 , GRCh37.p13 chr1: 143,376,429-143,384,527 , GRCh38.p12 chr14|NT_113796.3: 33,613-41,711 ANKRD20A15P, LOC105379271, 1 more genes
    esv3401186copy number variation1estd59human NCBI36 chr1: 142,217,852-142,223,250 , GRCh37.p13 chr1: 143,376,329-143,381,727 , GRCh38.p12 chr14|NT_113796.3: 33,513-38,911 ANKRD20A15P, LOC105379271
    esv3375111copy number variation1estd59human NCBI36 chr1: 142,183,352-142,226,150 , GRCh37.p13 chr1: 143,341,829-143,384,627 , GRCh38.p12 chr14|NT_113796.3: 1-41,811 ANKRD20A15P, LOC105379271, 1 more genes
    esv3368898copy number variation1estd59human NCBI36 chr1: 142,183,352-142,384,750 , GRCh37.p13 chr1: 143,341,829-143,543,227 , GRCh38.p12 chr14|NT_113796.3: 1-200,411 SNX18P20, SNX18P22, 3 more genes
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