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Items: 1 to 20 of 136

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5556604sequence alteration1nstd206human GRCh38 chr19: 38,269,810-38,604,627 , GRCh37.p13 chr19: 38,760,450-39,095,267 , PSMD8, 12 more genes
    nsv5027878copy number variation1nstd200human GRCh38 chr19: 38,408,209-38,408,372 , GRCh37.p13 chr19: 38,898,849-38,899,012 RASGRP4, FAM98C
    nsv4868290copy number variation1nstd200human GRCh37 chr19: 38,889,285-38,892,862 , GRCh38.p12 chr19: 38,398,645-38,402,222 FAM98C, SPRED3
    nsv4676223copy number variation1nstd102humanUncertain significance GRCh37 chr19: 38,512,717-39,291,526 , GRCh38.p12 chr19: 38,022,077-38,800,886 MAP4K1-AS1, LGALS7B, 25 more genes
    nsv4627564copy number variation1nstd183human GRCh37 chr19: 38,893,757-38,894,004 , GRCh38.p12 chr19: 38,403,117-38,403,364 FAM98C
    nsv4457372copy number variation1nstd102humanPathogenic GRCh37 chr19: 28,271,106-49,213,832 , GRCh38.p12 chr19: 27,780,198-48,710,575 ZNF461, LOC101927572, 735 more genes
    nsv4254152copy number variation1nstd166human GRCh37.p13 chr19: 38,888,986-38,901,189 , GRCh38.p12 chr19: 38,398,346-38,410,549 RASGRP4, SPRED3, 1 more genes
    nsv3913730copy number variation1nstd102humanPathogenic NCBI36 chr19: 11,199,618-49,821,491 , GRCh37 chr19: 11,338,618-45,129,651 , GRCh38 chr19: 11,227,942-44,626,354 BCKDHA, ADGRE5, 1102 more genes
    nsv3912447copy number variation1nstd102humanPathogenic NCBI36 chr19: 42,502,119-47,934,680 , GRCh37 chr19: 37,810,279-43,242,840 , GRCh38 chr19: 37,319,377-42,738,688 MIR8077, TRI-TAT1-1, 233 more genes
    nsv3904885copy number variation1nstd102humanPathogenic GRCh37 chr19: 68,029-59,110,290 , GRCh38.p12 chr19: 68,029-58,598,923 ZNF321P, ZNF861P, 2443 more genes
    nsv3903203copy number variation1nstd102humanPathogenic GRCh37 chr19: 260,912-59,097,160 , GRCh38.p12 chr19: 260,912-58,585,793 BABAM1, BEST2, 2426 more genes
    nsv3903092copy number variation2nstd102humanPathogenic GRCh37 chr19: 260,912-58,956,888 , GRCh38.p12 chr19: 260,912-58,445,521 LENG8, SYDE1, 2408 more genes
    nsv3895066copy number variation1nstd102humanPathogenic GRCh37 chr19: 37,582,250-41,630,908 , GRCh38.p12 chr19: 37,091,348-41,125,003 RNU6-140P, COQ8B, 162 more genes
    nsv3168446copy number variation1nstd158human GRCh37 chr19: 35,445,908-45,506,757 , GRCh38.p12 chr19: 34,955,004-45,003,499 , ACTN4, 449 more genes
    nsv3168420inversion1nstd158human GRCh37 chr19: 36,325,950-38,903,922 , GRCh38.p12 chr19: 35,835,048-38,413,282 APLP1, CAPNS1, 97 more genes
    nsv3167157copy number variation1nstd151human GRCh37 chr19: 38,869,878-38,903,940 , GRCh38.p12 chr19: 38,379,238-38,413,300 FAM98C, PSMD8, 3 more genes
    nsv3164901copy number variation1nstd151human GRCh37 chr19: 38,895,545-38,911,843 , GRCh38.p12 chr19: 38,404,905-38,421,203 RASGRP4, FAM98C
    nsv3163578copy number variation2nstd151human GRCh37 chr19: 38,895,545-38,900,739 , GRCh38.p12 chr19: 38,404,905-38,410,099 RASGRP4, FAM98C
    nsv3160620copy number variation1nstd151human GRCh37 chr19: 38,895,545-39,101,777 , GRCh38.p12 chr19: 38,404,905-38,611,137 , RASGRP4, 4 more genes
    nsv3159215copy number variation1nstd151human GRCh37 chr19: 38,845,348-39,071,149 , GRCh38.p12 chr19: 38,354,708-38,580,509 , FAM98C, 6 more genes
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