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Items: 16

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    Number of Variants: 16

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv4372152copy number variation236nstd173human GRCh37 chr6: 78,969,092-79,035,184 , GRCh38.p12 chr6: 78,259,375-78,325,467 LOC105377865
    nsv4376284copy number variation379nstd173human GRCh37 chr14: 41,608,616-41,657,457 , GRCh38.p12 chr14: 41,139,413-41,188,254 LINC02315
    nsv4368029copy number variation55nstd173human GRCh37 chr10: 68,077,579-68,122,519 , GRCh38.p12 chr10: 66,317,821-66,362,761 CTNNA3
    nsv4365428copy number variation2nstd173human GRCh37 chr19: 43,804,762-43,839,699 , GRCh38.p12 chr19: 43,300,610-43,335,547 CEACAMP4
    nsv4371674copy number variation102nstd173human GRCh37 chr3: 89,394,610-89,419,375 , GRCh38.p12 chr3: 89,345,460-89,370,225 EPHA3
    nsv4385455copy number variation190nstd173human GRCh37 chr20: 1,557,177-1,597,997 , GRCh38.p12 chr20: 1,576,531-1,617,351 SIRPB1
    nsv4376456copy number variation1782nstd173human GRCh37 chr8: 39,246,772-39,386,964 , GRCh38.p12 chr8: 39,389,253-39,529,445 ADAM5, ADAM3A
    nsv4383400copy number variation2nstd173human GRCh37 chr20: 41,253,081-41,278,809 , GRCh38.p12 chr20: 42,624,441-42,650,169 LOC105372624, PTPRT
    nsv4368298copy number variation45nstd173human GRCh37 chrX: 62,432,151-62,505,606 , GRCh38.p12 chrX: 63,212,272-63,285,729 LOC100533730, LOC105377212
    nsv4384114copy number variation32nstd173human GRCh37 chr17: 44,187,492-44,288,442 , GRCh38.p12 chr17: 46,110,126-46,211,076 , GRCh38.p12 chr17|NT_187663.1: 812,225-913,250 KANSL1-AS1, LOC107985027, 1 more genes
    nsv4376452copy number variation337nstd173human GRCh37 chr17: 34,437,494-34,477,480 , GRCh38.p12 chr17: 36,110,101-36,150,098 , GRCh38.p12 chr17|NT_187661.1: 64,198-104,195 , GRCh38.p12 chr17|NT_187614.1: 345,022-385,008 LOC101927369, LOC107985055, 3 more genes
    nsv4371991copy number variation196nstd173human GRCh37 chr19: 20,596,118-20,720,705 , GRCh38.p12 chr19: 20,413,312-20,537,899 ZNF826P, ZNF737, 4 more genes
    nsv4374121copy number variation41nstd173human GRCh37 chr2: 52,738,983-52,781,399 , GRCh38.p12 chr2: 52,511,845-52,554,261 0
    nsv4387125copy number variation432nstd173human GRCh37 chr2: 35,967,123-35,997,473 , GRCh38.p12 chr2: 35,742,057-35,772,407 0
    nsv4384501copy number variation242nstd173human GRCh37 chr16: 19,945,795-19,965,942 , GRCh38.p12 chr16: 19,934,473-19,954,620 0
    nsv4382973copy number variation317nstd173human GRCh37 chr5: 180,378,754-180,442,428 , GRCh38.p12 chr5: 180,951,754-181,015,428 BTNL3, LOC100128762, 4 more genes
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