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Items: 1 to 20 of 117

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7097127copy number variation1nstd102humanLikely pathogenic GRCh37 chr5: 141,333,097-141,335,037 , GRCh38.p12 chr5: 141,953,532-141,955,472 PCDH12
    nsv7057082inversion1nstd229human GRCh38 chr5: 139,208,712-142,493,851 , GRCh37.p13 chr5: 138,544,401-141,873,416 SPRY4-AS1, SPRY4, 151 more genes
    nsv6785934copy number variation1nstd229human GRCh38 chr5: 141,174,601-142,728,000 , GRCh37.p13 chr5: 140,687,717-142,107,565 TAF7, RNF14, 64 more genes
    nsv6785890copy number variation1nstd229human GRCh38 chr5: 141,946,577-141,946,710 , GRCh37.p13 chr5: 141,326,142-141,326,275 PCDH12, DELE1
    nsv6783847copy number variation1nstd229human GRCh38 chr5: 141,571,701-141,987,500 , GRCh37.p13 chr5: 140,951,268-141,367,065 DIAPH1, ARAP3, 10 more genes
    nsv6405955copy number variation1nstd223human GRCh38 chr5: 141,897,529-141,988,493 , GRCh37.p13 chr5: 141,277,094-141,368,058 PCDH12, RNF14, 1 more genes
    nsv6405600copy number variation1nstd223human GRCh38 chr5: 137,606,101-142,582,700 , GRCh37.p13 chr5: 136,941,790-141,962,265 TMCO6, PCDHB17P, 191 more genes
    nsv6135653copy number variation1nstd213human GRCh37 chr5: 138,340,000-143,460,001 , GRCh38.p12 chr5: 139,004,311-144,080,436 CD14, DIAPH1, 170 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
    nsv5901287copy number variation1nstd209human GRCh38 chr5: 141,632,244-142,199,968 , GRCh37.p13 chr5: 141,011,811-141,579,533 LOC107986454, NDFIP1, 13 more genes
    nsv5894078copy number variation1nstd209human GRCh38 chr5: 141,632,148-142,199,870 , GRCh37.p13 chr5: 141,011,715-141,579,435 DELE1, LOC729080, 13 more genes
    nsv5462685copy number variation1nstd206human GRCh38 chr5: 141,946,915-141,947,005 , GRCh37.p13 chr5: 141,326,480-141,326,570 DELE1, PCDH12
    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
    nsv4457090copy number variation1nstd102humanUncertain significance GRCh37 chr5: 140,424,333-148,985,999 , GRCh38.p12 chr5: 141,044,748-149,606,436 PCDHGC4, CKS1BP5, 165 more genes
    nsv4436202copy number variation1nstd102humanUncertain significance GRCh37 chr5: 14,685,137-149,511,942 , GRCh38.p12 chr5: 14,685,028-150,132,379 RNU1-150P, RNU6-727P, 1757 more genes
    nsv4320566inversion1nstd166human GRCh37.p13 chr5: 114,283,102-148,759,757 , GRCh38.p12 chr5: 114,947,405-149,380,194 , ACTBP4, 606 more genes
    nsv3960878insertion1nstd168human GRCh38 chr5: 141,949,459-142,017,040 , GRCh37.p13 chr5: 141,329,024-141,396,605 RNF14, DELE1, 2 more genes
    nsv3924856copy number variation1nstd102humanPathogenic NCBI36 chr5: 140,449,756-148,890,434 , GRCh37 chr5: 140,469,572-148,910,241 , GRCh38 chr5: 141,089,988-149,530,678 CTB-99A3.1, C5orf46, 160 more genes
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