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Items: 10

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    Number of Variants: 10

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv872690copy number variation8nstd71human NCBI36 chr1: 187,586,398-187,815,034 , GRCh37.p13 chr1: 189,319,775-189,548,411 , GRCh38.p12 chr1: 189,350,645-189,579,281 LOC105371657
    nsv886268copy number variation64nstd71human NCBI36 chr6: 79,031,809-79,098,352 , GRCh37.p13 chr6: 78,975,090-79,041,633 , GRCh38.p12 chr6: 78,265,373-78,331,916 LOC105377865
    nsv878052copy number variation17nstd71human NCBI36 chr3: 185,172,959-185,203,270 , GRCh37.p13 chr3: 183,690,265-183,720,576 , GRCh38.p12 chr3: 183,972,477-184,002,788 ABCC5
    nsv909839copy number variation966nstd71human NCBI36 chr18: 64,895,268-64,909,808 , GRCh37.p13 chr18: 66,744,288-66,758,828 , GRCh38.p12 chr18: 69,077,051-69,091,591 CCDC102B
    nsv882900copy number variation3nstd71human NCBI36 chr5: 131,690,961-131,703,880 , GRCh37.p13 chr5: 131,663,062-131,675,981 , GRCh38.p12 chr5: 132,327,369-132,340,288 SLC22A4, MIR3936HG
    nsv906184copy number variation11nstd71human NCBI36 chr16: 32,438,272-32,579,320 , GRCh37.p13 chr16: 32,530,771-32,671,819 , GRCh38.p12 chr16: 32,519,450-32,660,498 LOC107984013, FAM153DP
    nsv911913copy number variation63nstd71human NCBI36 chr19: 48,060,801-48,166,539 , GRCh37.p13 chr19: 43,368,961-43,474,699 , GRCh38.p12 chr19: 42,864,809-42,970,547 PSG1, CEACAMP7, 2 more genes
    nsv879310copy number variation1929nstd71human NCBI36 chr4: 69,076,346-69,179,871 , GRCh37.p13 chr4: 69,393,751-69,497,276 , GRCh38.p12 chr4: 68,528,033-68,631,558 LOC100422402, LOC100132651, 2 more genes
    nsv883554copy number variation1nstd71human NCBI36 chr6: 29,948,627-29,967,687 , GRCh37.p13 chr6: 29,840,648-29,859,708 , GRCh38.p12 chr6: 29,872,871-29,891,931 HCP5B, HCG4P7, 1 more genes
    nsv904023copy number variation257nstd71human NCBI36 chr15: 32,487,589-32,625,184 , GRCh37.p13 chr15: 34,700,297-34,837,892 , GRCh38.p12 chr15: 34,408,096-34,545,691 LOC100422491, GOLGA8B, 5 more genes
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