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Items: 1 to 20 of 4347

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6137756copy number variation1nstd102humanBenign GRCh38 chr4: 5,748,550-5,748,617 , GRCh37 chr4: 5,750,277-5,750,344 EVC
    nsv6131661insertion1nstd186human GRCh37 chr16: 90,107,059-90,107,059 , GRCh38.p12 chr16: 90,040,651-90,040,651 GAS8, URAHP
    nsv6112761copy number variation1nstd102humanPathogenic GRCh37 chr4: 69,671-29,702,595 , GRCh38.p12 chr4: 69,779-29,700,973 LOC101928306, PDE6B-AS1, 460 more genes
    nsv6112747copy number variation1nstd102humanPathogenic GRCh37 chr4: 68,598-18,912,995 , GRCh38.p12 chr4: 68,706-18,911,372 GPR78, LOC105374510, 362 more genes
    nsv5979532inversion1nstd209human GRCh38 chr4: 4,147,913-9,493,295 , GRCh37.p13 chr4: 4,149,640-9,494,939 , CRMP1, 130 more genes
    nsv5979177inversion1nstd209human GRCh38 chr11: 125,961,131-125,961,366 , GRCh37.p13 chr11: 125,831,026-125,831,261 CDON
    nsv5977822insertion1nstd209human GRCh38 chr17: 4,709,638-4,709,638 , GRCh37.p13 chr17: 4,612,933-4,612,933 ARRB2
    nsv5974394inversion1nstd209human GRCh38 chr4: 4,005,086-9,639,734 , GRCh37.p13 chr4: 4,006,813-9,641,358 , CRMP1, 142 more genes
    nsv5973695insertion1nstd209human GRCh38 chr16: 90,040,651-90,040,651 , GRCh37.p13 chr16: 90,107,059-90,107,059 GAS8, URAHP
    nsv5973087inversion1nstd209human GRCh38 chr4: 3,883,398-8,956,544 , GRCh37.p13 chr4: 3,885,125-8,958,270 , CRMP1, 102 more genes
    nsv5971133insertion1nstd209human GRCh38 chr11: 75,300,677-75,300,677 , GRCh37.p13 chr11: 75,011,721-75,011,721 ARRB1
    nsv5969980insertion1nstd209human GRCh38 chr11: 67,274,495-67,274,495 , GRCh37.p13 chr11: 67,041,966-67,041,966 GRK2
    nsv5964709insertion1nstd209human GRCh38 chr4: 5,732,021-5,732,021 , GRCh37.p13 chr4: 5,733,748-5,733,748 EVC
    nsv5962525insertion1nstd209human GRCh38 chr4: 5,658,601-5,658,601 , GRCh37.p13 chr4: 5,660,328-5,660,328 EVC2
    nsv5959039insertion1nstd209human GRCh38 chr4: 5,808,133-5,808,133 , GRCh37.p13 chr4: 5,809,860-5,809,860 EVC
    nsv5958408insertion1nstd209human GRCh38 chr3: 113,236,288-113,236,288 , GRCh37.p13 chr3: 112,955,135-112,955,135 BOC
    nsv5955995insertion1nstd209human GRCh38 chr4: 5,666,267-5,666,267 , GRCh37.p13 chr4: 5,667,994-5,667,994 EVC2
    nsv5953104insertion1nstd209human GRCh38 chr5: 149,537,754-149,537,754 , GRCh37.p13 chr5: 148,917,317-148,917,317 CSNK1A1
    nsv5951279insertion1nstd209human GRCh38 chr4: 5,748,793-5,748,793 , GRCh37.p13 chr4: 5,750,520-5,750,520 EVC
    nsv5945275copy number variation1nstd209human GRCh38 chr16: 90,023,591-90,023,955 , GRCh37.p13 chr16: 90,089,999-90,090,363 GAS8
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