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Items: 1 to 20 of 98

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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
    nsv6792308copy number variation1nstd229human GRCh38 chr5: 150,402,626-150,406,258 , GRCh37.p13 chr5: 149,782,189-149,785,821 CD74
    nsv6785531copy number variation1nstd229human GRCh38 chr5: 150,402,627-150,404,679 , GRCh37.p13 chr5: 149,782,190-149,784,242 CD74
    nsv6781989copy number variation1nstd229human GRCh38 chr5: 150,409,729-150,438,872 , GRCh37.p13 chr5: 149,789,292-149,818,435 CD74
    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
    nsv6630116copy number variation1nstd224human GRCh37 chr5: 149,755,421-149,810,153 , GRCh38.p12 chr5: 150,375,858-150,430,590 TCOF1, CD74
    nsv6414572copy number variation1nstd223human GRCh38 chr5: 150,374,196-150,438,419 , GRCh37.p13 chr5: 149,753,759-149,817,982 CD74, TCOF1
    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
    nsv5673660copy number variation1nstd102humanPathogenic GRCh37 chr5: 149,775,825-149,778,631 , GRCh38.p12 chr5: 150,396,262-150,399,068 CD74, TCOF1
    nsv5036421inversion1nstd200human GRCh38 chr5: 85,193,812-162,906,830 , GRCh37.p13 chr5: 84,489,630-162,333,836 , PRR16, 1116 more genes
    nsv4949085copy number variation1nstd200human GRCh38 chr5: 150,374,196-150,438,421 , GRCh37.p13 chr5: 149,753,759-149,817,984 CD74, TCOF1
    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
    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
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