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Items: 1 to 20 of 247

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7098718copy number variation1nstd102humanUncertain significance GRCh37 chr19: 1,206,913-3,771,740 , GRCh38.p12 chr19: 1,206,914-3,771,742 GIPC3, GNG7, 117 more genes
    nsv7095297copy number variation1nstd102humanUncertain significance GRCh37 chr19: 589,946-5,696,788 , GRCh38.p12 chr19: 589,946-5,696,777 NCLN, RN7SL202P, 223 more genes
    nsv7095296copy number variation1nstd102humanUncertain significance GRCh37 chr19: 589,946-2,151,333 , GRCh38.p12 chr19: 589,946-2,151,334 ADAMTSL5, GPX4, 90 more genes
    nsv7095264copy number variation1nstd102humanPathogenic GRCh37 chr19: 1,206,913-1,650,247 , GRCh38.p12 chr19: 1,206,914-1,650,248 NDUFS7, GAMT, 30 more genes
    nsv7095226copy number variation1nstd102humanUncertain significance GRCh37 chr19: 589,946-4,818,389 , GRCh38.p12 chr19: 589,946-4,818,377 ATP5F1D, LOC102723798, 204 more genes
    nsv7011003copy number variation1nstd229human GRCh38 chr19: 1,393,408-1,409,654 , GRCh37.p13 chr19: 1,393,407-1,409,653 GAMT, NDUFS7, 1 more genes
    nsv6998176copy number variation1nstd229human GRCh38 chr19: 1,354,337-1,412,999 , GRCh37.p13 chr19: 1,354,336-1,412,998 TRF-GAA1-6, PWWP3A, 4 more genes
    nsv6637582copy number variation1nstd102humanUncertain significance GRCh37 chr19: 1,356,893-1,676,446 , GRCh38.p12 chr19: 1,356,894-1,676,447 REEP6, GAMT, 18 more genes
    nsv6637184copy number variation1nstd102humanPathogenic GRCh37 chr19: 1,205,244-1,479,188 , GRCh38.p12 chr19: 1,205,245-1,479,189 C19orf25, EFNA2, 19 more genes
    nsv6315518copy number variation1nstd102humanPathogenic GRCh37 chr19: 260,911-2,256,387 , GRCh38.p12 chr19: 260,911-2,256,388 LOC100420586, RPS15, 113 more genes
    nsv6315133copy number variation1nstd102humanUncertain significance GRCh37 chr19: 1,397,025-1,397,484 , GRCh38.p12 chr19: 1,397,026-1,397,485 GAMT
    nsv6310468copy number variation1nstd102humanPathogenic GRCh37 chr19: 1,398,895-1,401,475 , GRCh38.p12 chr19: 1,398,896-1,401,476 GAMT
    nsv6188429copy number variation1nstd214human GRCh38 chr19: 1,399,984-1,400,138 , GRCh37.p13 chr19: 1,399,983-1,400,137 GAMT
    nsv6133707copy number variation1nstd213human GRCh37 chr19: 560,000-1,700,001 , GRCh38.p12 chr19: 560,000-1,700,002 ATP5F1D, AZU1, 73 more genes
    nsv6133692copy number variation1nstd213human GRCh37 chr19: 180,000-2,200,001 , GRCh38.p12 chr19: 180,000-2,200,002 ATP5F1D, AZU1, 113 more genes
    nsv6102682inversion1nstd212human GRCh38 chr19: 871,904-2,377,665 , GRCh37.p13 chr19: 871,904-2,377,663 AMH, ATP5F1D, 83 more genes
    nsv5930880copy number variation1nstd209human GRCh38 chr19: 1,397,159-1,397,225 , GRCh37.p13 chr19: 1,397,158-1,397,224 GAMT
    nsv5673233copy number variation1nstd102humanPathogenic GRCh37 chr19: 1,387,800-1,401,485 , GRCh38.p12 chr19: 1,387,801-1,401,486 GAMT, NDUFS7
    nsv5293566copy number variation1nstd204human GRCh38.p13 chr19: 1,197,501-1,413,600 , GRCh37.p13 chr19: 1,197,500-1,413,599 CBARP, RPS15P9, 17 more genes
    nsv5291342copy number variation1nstd204human GRCh38.p13 chr19: 879,901-2,550,600 , GRCh37.p13 chr19: 879,901-2,550,598 LOC105372240, ELOCP28, 92 more genes
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