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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6314386complex chromosomal rearrangement5nstd102humanUncertain significance GRCh38.p12 chr16: 55,052,894-55,052,894 , GRCh38.p12 chr16: 55,052,894-55,052,894 , GRCh37 chr16: 55,086,806-55,086,806 , GRCh37 chr16: 55,086,806-55,086,806 , GRCh38.p12 chr10: 84,763,363-84,763,363 , GRCh38.p12 chr10: 48,925,282-48,925,282 , GRCh38.p12 chr10: 48,925,288-48,925,288 , GRCh38.p12 chr10: 84,762,420-84,762,420 , GRCh37 chr10: 86,523,119-86,523,119 , GRCh37 chr10: 50,133,327-50,133,327 , GRCh37 chr10: 50,133,333-50,133,333 , GRCh37 chr10: 86,522,176-86,522,176 , GRCh38.p12 chr9: 102,842,491-102,842,491 , GRCh38.p12 chr9: 102,842,491-102,842,491 , GRCh37 chr9: 105,604,773-105,604,773 , GRCh37 chr9: 105,604,773-105,604,773 , GRCh37 chr7: 118,838,492-118,838,492 , GRCh37 chr7: 118,838,590-118,838,590 , GRCh38.p12 chr7: 119,198,438-119,198,438 , GRCh38.p12 chr7: 119,198,536-119,198,536 LRRC18, WDFY4
    nsv7137209copy number variation1nstd102humanPathogenic GRCh37 chr10: 12,829,206-135,427,143 , GRCh38.p12 chr10: 12,787,207-133,613,639 LRRC18, RNU7-12P, 1876 more genes
    nsv4675455copy number variation1nstd102humanPathogenic GRCh37 chr10: 50,250,603-69,256,083 , GRCh38.p12 chr10: 45,931,517-67,496,325 LRRC18, MRLN, 242 more genes
    nsv3919674copy number variation1nstd102humanPathogenic NCBI36 chr10: 49,100,986-52,085,077 , GRCh38 chr10: 45,931,517-50,655,311 , GRCh37 chr10: 49,430,980-52,415,071 LRRC18, AGAP12P, 111 more genes
    nsv3911796copy number variation1nstd102humanPathogenic NCBI36 chr10: 45,525,696-51,581,091 , GRCh38 chr10: 45,710,242-50,151,325 , GRCh37 chr10: 46,205,690-51,911,085 LRRC18, AGAP4, 111 more genes
    nsv3891326copy number variation1nstd102humanPathogenic GRCh37 chr10: 46,225,364-51,874,356 , GRCh38.p12 chr10: 45,729,916-50,114,596 LRRC18, AGAP9, 108 more genes
    nsv4455118copy number variation1nstd102humanPathogenic GRCh37 chr10: 46,235,357-51,874,163 , GRCh38.p12 chr10: 45,739,909-50,114,403 LRRC18, DUSP8P2, 108 more genes
    nsv7148121copy number variation1nstd102humanPathogenic GRCh37 chr10: 46,284,269-51,870,080 , GRCh38.p12 chr10: 45,788,821-50,110,320 LRRC18, LOC100420617, 108 more genes
    nsv3917908copy number variation1nstd102humanPathogenic GRCh38 chr10: 45,710,248-50,021,141 , GRCh37 chr10: 46,205,696-51,724,915 , NCBI36 chr10: 45,525,702-51,450,907 LRRC18, LINC02675, 108 more genes
    nsv3896419copy number variation1nstd102humanPathogenic GRCh37 chr10: 46,287,821-51,861,565 , GRCh38.p12 chr10: 45,792,373-50,101,805 LRRC18, RHEBP1, 108 more genes
    nsv3917450copy number variation1nstd102humanPathogenic GRCh38 chr10: 45,710,242-49,929,364 , GRCh37 chr10: 46,205,690-51,330,432 , NCBI36 chr10: 45,525,696-51,265,056 LRRC18, ANXA8L1, 102 more genes
    nsv3895921copy number variation2nstd102humanPathogenic GRCh37 chr10: 46,966,533-51,903,755 , GRCh38.p12 chr10: 45,931,517-50,143,995 LRRC18, LINC02637, 104 more genes
    nsv3891496copy number variation1nstd102humanPathogenic GRCh37 chr10: 46,224,446-51,594,991 , GRCh38.p12 chr10: 45,728,998-49,929,364 LRRC18, ARHGAP22-IT1, 100 more genes
    nsv3904341copy number variation1nstd102humanPathogenic GRCh37 chr10: 46,966,533-51,874,356 , GRCh38.p12 chr10: 45,931,517-50,114,596 LRRC18, AGAP7P, 104 more genes
    nsv6634443copy number variation1nstd102humanPathogenic GRCh37 chr10: 46,287,821-51,627,470 , GRCh38.p12 chr10: 45,792,373-49,929,364 LRRC18, GLUD1P2, 100 more genes
    nsv4716588copy number variation1nstd102humanPathogenic GRCh37 chr10: 46,964,973-51,826,226 , GRCh38.p12 chr10: 45,931,517-50,066,466 LRRC18, MAPK8, 104 more genes
    nsv4350671copy number variation1nstd102humanPathogenic GRCh37 chr10: 46,544,810-51,743,471 , GRCh38.p12 chr10: 45,931,517-49,983,711 LRRC18, RNA5SP315, 100 more genes
    nsv6315547copy number variation1nstd102humanPathogenic GRCh37 chr10: 46,576,515-51,680,164 , GRCh38.p12 chr10: 45,931,517-49,929,364 LRRC18, ARHGAP22-IT1, 96 more genes
    nsv3902493copy number variation1nstd102humanPathogenic GRCh37 chr10: 46,966,533-51,700,837 , GRCh38.p12 chr10: 45,931,517-49,929,364 LRRC18, PTPN20, 96 more genes
    nsv6315565copy number variation1nstd102humanPathogenic GRCh37 chr10: 49,378,356-52,467,181 , GRCh38.p12 chr10: 45,999,930-49,959,916 LRRC18, HNRNPA1P33, 95 more genes
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