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Items: 1 to 20 of 195

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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
    nsv7039118inversion1nstd229human GRCh38 chr5: 150,504,385-150,506,753 , GRCh37.p13 chr5: 149,883,947-149,886,315 NDST1
    nsv7038217inversion1nstd229human GRCh38 chr5: 142,898,166-151,101,968 , GRCh37.p13 chr5: 142,277,731-150,481,529 RPS20P4, PPARGC1B, 126 more genes
    nsv6794956copy number variation1nstd229human GRCh38 chr5: 150,516,701-150,518,813 , GRCh37.p13 chr5: 149,896,263-149,898,375 NDST1
    nsv6794404copy number variation1nstd229human GRCh38 chr5: 150,550,705-150,551,044 , GRCh37.p13 chr5: 149,930,267-149,930,606 NDST1
    nsv6794337copy number variation1nstd229human GRCh38 chr5: 150,493,014-150,495,944 , GRCh37.p13 chr5: 149,872,576-149,875,506 NDST1
    nsv6779186copy number variation1nstd229human GRCh38 chr5: 150,232,549-150,518,402 , GRCh37.p13 chr5: 149,612,112-149,897,964 RPS14, NDST1, 7 more genes
    nsv6778801copy number variation1nstd229human GRCh38 chr5: 150,494,354-150,497,931 , GRCh37.p13 chr5: 149,873,916-149,877,493 NDST1
    nsv6414691copy number variation1nstd223human GRCh38 chr5: 150,516,714-150,518,787 , GRCh37.p13 chr5: 149,896,276-149,898,349 NDST1
    nsv6411201copy number variation1nstd223human GRCh38 chr5: 150,493,010-150,495,945 , GRCh37.p13 chr5: 149,872,572-149,875,507 NDST1
    nsv6409709copy number variation1nstd223human GRCh38 chr5: 150,494,321-150,497,977 , GRCh37.p13 chr5: 149,873,883-149,877,539 NDST1
    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
    nsv6284946insertion1nstd214human GRCh38 chr5: 150,531,983-150,531,983 , GRCh37.p13 chr5: 149,911,545-149,911,545 NDST1
    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
    nsv6005437copy number variation1nstd212human GRCh38 chr5: 150,533,949-150,534,035 , GRCh37.p13 chr5: 149,913,511-149,913,597 NDST1
    nsv5894476copy number variation1nstd209human GRCh38 chr5: 150,516,688-150,518,798 , GRCh37.p13 chr5: 149,896,250-149,898,360 NDST1
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