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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6313224copy number variation1nstd102humanPathogenic GRCh37 chrX: 46,712,891-46,719,557 , GRCh38.p12 chrX: 46,853,456-46,860,122 RP2
    nsv6313225copy number variation1nstd102humanPathogenic GRCh37 chrX: 46,736,920-46,739,204 , GRCh38.p12 chrX: 46,877,485-46,879,769 RP2
    nsv4683378copy number variation1nstd102humanPathogenic GRCh37 chrX: 46,736,940-46,739,204 , GRCh38.p12 chrX: 46,877,505-46,879,769 RP2
    nsv7098665copy number variation1nstd102humanPathogenic GRCh37 chrX: 46,719,403-46,719,557 , GRCh38.p12 chrX: 46,859,968-46,860,122 RP2
    nsv997134copy number variation1nstd45humanPathogenic GRCh37 chrX: 46,696,347-46,741,793 , GRCh38.p12 chrX: 46,836,912-46,882,358 RP2
    nsv6313223copy number variation2nstd102humanPathogenic, Uncertain significance GRCh37 chrX: 46,696,536-46,696,657 , GRCh38.p12 chrX: 46,837,101-46,837,222 RP2
    nsv7093560insertion1nstd102humanPathogenic GRCh37 chrX: 46,719,482-46,719,482 , GRCh38 chrX: 46,860,047-46,860,047 RP2
    nsv7098534copy number variation1nstd102humanLikely pathogenic GRCh37 chrX: 46,713,474-46,714,179 , GRCh38.p12 chrX: 46,854,039-46,854,744 RP2
    nsv5674148copy number variation1nstd102humanLikely pathogenic GRCh37 chrX: 46,712,891-46,713,596 , GRCh38.p12 chrX: 46,853,456-46,854,161 RP2
    nsv6313373copy number variation1nstd102humanLikely pathogenic GRCh37 chrX: 46,739,101-46,739,204 , GRCh38.p12 chrX: 46,879,666-46,879,769 RP2
    nsv3904062copy number variation1nstd102humanBenign GRCh37 chr10: 114,351,353-114,378,132 , GRCh38.p12 chr10: 112,591,594-112,618,373 VTI1A
    nsv6313372copy number variation1nstd102humanUncertain significance GRCh37 chrX: 46,696,346-46,741,794 , GRCh38.p12 chrX: 46,836,911-46,882,359 RP2
    nsv3895702copy number variation1nstd102humanLikely benign GRCh37 chr10: 114,195,933-114,306,003 , GRCh38.p12 chr10: 112,436,175-112,546,244 ZDHHC6, VTI1A
    nsv3921477copy number variation1nstd102humanUncertain significance NCBI36 chr10: 114,288,301-114,414,465 , GRCh37.p13 chr10: 114,298,311-114,424,475 , GRCh38.p12 chr10: 112,538,552-112,664,716 MIR4295, VTI1A
    nsv7098416copy number variation1nstd102humanPathogenic GRCh37 chrX: 46,480,392-46,739,204 , GRCh38.p12 chrX: 46,620,957-46,879,769 RP2, YBX1P8, 3 more genes
    nsv4683158copy number variation1nstd102humanPathogenic GRCh37 chrX: 46,719,423-46,952,346 , GRCh38.p12 chrX: 46,859,988-47,092,947 RP2, JADE3, 3 more genes
    nsv5674147copy number variation1nstd102humanPathogenic GRCh37 chrX: 46,508,101-46,739,204 , GRCh38.p12 chrX: 46,648,666-46,879,769 RP2, YBX1P8, 2 more genes
    nsv7098663copy number variation2nstd102humanUncertain significance, Pathogenic GRCh37 chrX: 46,466,387-46,719,557 , GRCh38.p12 chrX: 46,606,952-46,860,122 RP2, SLC9A7, 3 more genes
    nsv3871691copy number variation1nstd102humanBenign GRCh37 chr1: 94,228,900-94,330,992 , GRCh38.p12 chr1: 93,763,344-93,865,436 DNTTIP2, TRR-TCT1-1, 2 more genes
    nsv6314015copy number variation1nstd102humanUncertain significance GRCh37 chr19: 33,146,131-33,251,180 , GRCh38.p12 chr19: 32,655,225-32,760,274 RN7SL789P, NUDT19, 3 more genes
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