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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
    nsv5970408inversion1nstd209human GRCh38 chr19: 2,282,477-7,636,587 , GRCh37.p13 chr19: 2,282,476-7,701,473 , TLE5, 195 more genes
    nsv5522838copy number variation1nstd206human GRCh38 chr19: 2,457,401-2,460,402 , GRCh37.p13 chr19: 2,457,399-2,460,400 LMNB2, LINC01775
    nsv5292953copy number variation1nstd204human GRCh38.p13 chr19: 2,349,101-2,713,600 , GRCh37.p13 chr19: 2,349,099-2,713,598 TMPRSS9, RNU6-993P, 11 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
    nsv5185163mobile element insertion1nstd203human GRCh38 chr19: 2,458,349-2,458,379 , GRCh37.p13 chr19: 2,458,347-2,458,377 LINC01775
    nsv5036059inversion1nstd200human GRCh38 chr19: 2,458,654-2,459,174 , GRCh37.p13 chr19: 2,458,652-2,459,172 LINC01775
    nsv5014317copy number variation1nstd200human GRCh38 chr19: 2,460,559-2,465,405 , GRCh37.p13 chr19: 2,460,557-2,465,403 LINC01775
    nsv4885520inversion1nstd200human GRCh37 chr19: 2,458,652-2,459,172 , GRCh38.p12 chr19: 2,458,654-2,459,174 LINC01775
    nsv4684376copy number variation1nstd102humanUncertain significance GRCh37 chr19: 2,273,150-2,897,133 , GRCh38.p12 chr19: 2,273,151-2,897,135 LOC101928572, TIMM13, 24 more genes
    nsv4681096copy number variation1nstd102humanUncertain significance GRCh37 chr19: 2,456,648-2,456,951 , GRCh38.p12 chr19: 2,456,650-2,456,953 LINC01775, LMNB2
    nsv4676346copy number variation1nstd102humanPathogenic GRCh37 chr19: 260,911-3,501,271 , GRCh38.p12 chr19: 260,911-3,501,273 AZU1, REEP6, 159 more genes
    nsv4676189copy number variation1nstd102humanPathogenic GRCh37 chr19: 260,912-4,384,674 , GRCh38.p12 chr19: 260,912-4,384,677 MRPL54, DAZAP1, 198 more genes
    nsv4621272copy number variation1nstd183human GRCh37 chr19: 2,145,005-2,466,296 , GRCh38.p12 chr19: 2,145,006-2,466,298 LMNB2, LINC01775, 19 more genes
    nsv4457798copy number variation1nstd102humanUncertain significance GRCh37 chr19: 2,389,731-2,925,532 , GRCh38.p12 chr19: 2,389,733-2,925,534 MIR7108, THOP1, 19 more genes
    nsv4457776copy number variation1nstd102humanPathogenic GRCh37 chr19: 260,911-4,788,357 , GRCh38.p12 chr19: 260,911-4,788,345 BSG, LOC100420586, 217 more genes
    nsv4452268copy number variation1nstd102humanUncertain significance GRCh37 chr19: 1,406,030-3,597,207 , GRCh38.p12 chr19: 1,406,031-3,597,209 C19orf25, MIR7108, 92 more genes
    nsv4436611copy number variation1nstd102humanUncertain significance GRCh37 chr19: 2,229,488-4,004,142 , GRCh38.p12 chr19: 2,229,489-4,004,144 LMNB2, SF3A2, 76 more genes
    nsv3958851insertion1nstd168human GRCh38 chr19: 2,353,635-2,476,368 , GRCh37.p13 chr19: 2,353,633-2,476,366 GADD45B, TIMM13, 5 more genes
    nsv3924102copy number variation1nstd102humanPathogenic GRCh38 chr19: 259,395-6,795,611 , GRCh37 chr19: 259,395-6,795,622 , NCBI36 chr19: 210,395-6,746,622 POLR2E, PWWP3A, 283 more genes
    nsv3923561copy number variation1nstd102humanPathogenic NCBI36 chr19: 184,565-4,650,484 , GRCh37 chr19: 233,565-4,699,484 , GRCh38 chr19: 233,565-4,699,472 DAPK3, IZUMO4, 214 more genes
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