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Items: 1 to 20 of 202

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7053998inversion1nstd229human GRCh38 chr5: 148,749,982-154,424,819 , GRCh37.p13 chr5: 148,129,545-153,804,379 HMGXB3, RN7SL868P, 102 more genes
    nsv7053584inversion1nstd229human GRCh38 chr5: 144,534,922-150,861,041 , GRCh37.p13 chr5: 143,914,485-150,240,603 SMIM3, NAMPTP2, 102 more genes
    nsv7045608inversion1nstd229human GRCh38 chr5: 142,902,498-151,105,008 , GRCh37.p13 chr5: 142,282,063-150,484,569 FBXO38-DT, POU4F3, 126 more genes
    nsv7038217inversion1nstd229human GRCh38 chr5: 142,898,166-151,101,968 , GRCh37.p13 chr5: 142,277,731-150,481,529 RPS20P4, PPARGC1B, 126 more genes
    nsv6781593copy number variation1nstd229human GRCh38 chr5: 150,637,310-150,637,386 , GRCh37.p13 chr5: 150,016,872-150,016,948 SYNPO
    nsv6410999copy number variation1nstd223human GRCh38 chr5: 150,587,549-150,588,488 , GRCh37.p13 chr5: 149,967,111-149,968,050 SYNPO
    nsv6410639copy number variation1nstd223human GRCh38 chr5: 150,575,725-150,602,997 , GRCh37.p13 chr5: 149,955,287-149,982,559 SYNPO
    nsv6404156copy number variation1nstd223human GRCh38 chr5: 150,590,763-150,592,127 , GRCh37.p13 chr5: 149,970,325-149,971,689 SYNPO
    nsv6401175copy number variation1nstd223human GRCh38 chr5: 150,536,626-150,594,045 , GRCh37.p13 chr5: 149,916,188-149,973,607 NDST1, SYNPO
    nsv6315448copy number variation1nstd102humanPathogenic GRCh37 chr5: 149,010,383-180,719,789 , GRCh38.p12 chr5: 149,630,820-181,292,788 GRM6, MIR1229, 554 more genes
    nsv6300602copy number variation1nstd186human GRCh37 chr5: 149,978,568-149,978,675 , GRCh38.p12 chr5: 150,599,006-150,599,113 SYNPO
    nsv6292504mobile element insertion1nstd186human GRCh37 chr5: 149,976,756-149,976,807 , GRCh38.p12 chr5: 150,597,194-150,597,245 SYNPO
    nsv6244964mobile element insertion1nstd215human GRCh38 chr5: 150,620,928-150,620,928 , GRCh37.p13 chr5: 150,000,490-150,000,490 SYNPO
    nsv6135205copy number variation1nstd213human GRCh37 chr5: 91,690,000-180,740,001 , GRCh38.p12 chr5: 92,354,293-181,313,000 ADRA1B, ASS1P10, 1378 more genes
    nsv6135120copy number variation1nstd213human GRCh37 chr5: 143,910,000-152,670,001 , GRCh38.p12 chr5: 144,530,437-153,290,441 ADRB2, ANXA6, 143 more genes
    nsv5960053insertion1nstd209human GRCh38 chr5: 150,656,741-150,656,741 , GRCh37.p13 chr5: 150,036,303-150,036,303 SYNPO
    nsv5889133copy number variation1nstd209human GRCh38 chr5: 150,588,392-150,594,076 , GRCh37.p13 chr5: 149,967,954-149,973,638 SYNPO
    nsv5841489copy number variation1nstd209human GRCh38 chr5: 150,588,361-150,594,035 , GRCh37.p13 chr5: 149,967,923-149,973,597 SYNPO
    nsv5693062mobile element insertion1nstd211human GRCh38 chr5: 150,597,194-150,597,194 , GRCh37.p13 chr5: 149,976,756-149,976,756 SYNPO
    nsv5473469copy number variation1nstd206human GRCh38 chr5: 150,641,051-150,644,591 , GRCh37.p13 chr5: 150,020,613-150,024,153 SYNPO
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