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Items: 1 to 20 of 78

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7144441insertion1nstd232human GRCh37.p13 chr5: 150,075,272-150,075,272 , GRCh38.p12 chr5: 150,695,710-150,695,710 RBM22
    nsv7138263copy number variation1nstd232human GRCh37.p13 chr5: 150,076,267-150,076,351 , GRCh38.p12 chr5: 150,696,705-150,696,789 RBM22
    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
    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
    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
    nsv5189671mobile element insertion1nstd203human GRCh38 chr5: 150,694,564-150,694,579 , GRCh37.p13 chr5: 150,074,126-150,074,141 RBM22
    nsv5036421inversion1nstd200human GRCh38 chr5: 85,193,812-162,906,830 , GRCh37.p13 chr5: 84,489,630-162,333,836 , PRR16, 1116 more genes
    nsv4947215copy number variation1nstd200human GRCh38 chr5: 93,957,557-155,223,076 , GRCh37.p13 chr5: 93,293,262-154,602,636 , TGFBI, 937 more genes
    nsv4885569inversion1nstd200human GRCh37 chr5: 84,489,636-162,333,841 , GRCh38.p12 chr5: 85,193,818-162,906,835 , UBE2B, 1116 more genes
    nsv4590249copy number variation1nstd183human GRCh37 chr5: 150,058,753-150,079,999 , GRCh38.p12 chr5: 150,679,191-150,700,437 RBM22, MYOZ3
    nsv3923414copy number variation1nstd102humanPathogenic GRCh37 chr5: 130,196,621-154,701,371 , NCBI36 chr5: 130,224,520-154,681,564 , GRCh38 chr5: 130,860,928-155,321,811 HNRNPA3P7, RNU6-456P, 514 more genes
    nsv3921182copy number variation1nstd102humanPathogenic GRCh37 chr5: 149,094,155-180,699,152 , GRCh38 chr5: 149,714,592-181,272,151 , NCBI36 chr5: 149,074,348-180,631,758 RN7SKP148, TCOF1, 553 more genes
    nsv3914878copy number variation1nstd102humanPathogenic NCBI36 chr5: 146,520,648-163,194,778 , GRCh37.p13 chr5: 146,540,455-163,262,200 , GRCh38.p12 chr5: 147,160,892-163,835,194 LOC105378231, RN7SKP232, 247 more genes
    nsv3914009copy number variation1nstd102humanPathogenic NCBI36 chr5: 129,211,386-152,713,299 , GRCh38 chr5: 129,847,794-153,353,546 , GRCh37 chr5: 129,183,487-152,733,106 UQCRQ, SNHG4, 489 more genes
    nsv3912937copy number variation1nstd102humanPathogenic GRCh37 chr5: 105,955,289-155,551,397 , NCBI36 chr5: 105,983,188-155,483,975 , GRCh38 chr5: 106,619,588-156,124,387 LINC01023, CTB-99A3.1, 783 more genes
    nsv3912593copy number variation1nstd102humanUncertain significance NCBI36 chr5: 332,389-180,837,866 , GRCh37.p13 chr5: 279,389-180,905,260 , GRCh38.p12 chr5: 279,274-181,478,259 LOC105378993, LOC107986375, 2492 more genes
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