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Items: 1 to 20 of 179

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7057082inversion1nstd229human GRCh38 chr5: 139,208,712-142,493,851 , GRCh37.p13 chr5: 138,544,401-141,873,416 SPRY4-AS1, SPRY4, 151 more genes
    nsv6794591copy number variation1nstd229human GRCh38 chr5: 141,993,372-142,000,201 , GRCh37.p13 chr5: 141,372,937-141,379,766 GNPDA1
    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
    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
    nsv6405175copy number variation1nstd223human GRCh38 chr5: 141,993,372-142,000,199 , GRCh37.p13 chr5: 141,372,937-141,379,764 GNPDA1
    nsv6400776copy number variation1nstd223human GRCh38 chr5: 142,010,436-142,010,760 , GRCh37.p13 chr5: 141,390,001-141,390,325 GNPDA1
    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
    nsv6079154insertion1nstd212human GRCh38 chr5: 142,000,058-142,000,058 , GRCh37.p13 chr5: 141,379,623-141,379,623 GNPDA1
    nsv6062770insertion1nstd212human GRCh38 chr5: 142,000,088-142,000,088 , GRCh37.p13 chr5: 141,379,653-141,379,653 GNPDA1
    nsv5949944insertion1nstd209human GRCh38 chr5: 142,000,088-142,000,088 , GRCh37.p13 chr5: 141,379,653-141,379,653 GNPDA1
    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
    nsv5693123mobile element insertion1nstd211human GRCh38 chr5: 142,013,219-142,013,219 , GRCh37.p13 chr5: 141,392,784-141,392,784 GNPDA1
    nsv5626564insertion1nstd207human GRCh38 chr5: 142,000,088-142,000,088 , GRCh37.p13 chr5: 141,379,653-141,379,653 GNPDA1
    nsv5361830translocation1nstd200human GRCh38 chr5: 142,000,104-142,000,104 , GRCh38 chr3: 106,110,017-106,110,017 , GRCh37.p13 chr3: 105,828,864-105,828,864 , GRCh37.p13 chr5: 141,379,669-141,379,669 GNPDA1
    nsv5094136mobile element insertion1nstd203human GRCh38 chr5: 142,000,087-142,000,087 , GRCh37.p13 chr5: 141,379,652-141,379,652 GNPDA1
    nsv5092729mobile element insertion1nstd203human GRCh38 chr5: 142,000,089-142,000,104 , GRCh37.p13 chr5: 141,379,654-141,379,669 GNPDA1
    nsv5088334mobile element insertion1nstd203human GRCh38 chr5: 142,000,095-142,000,104 , GRCh37.p13 chr5: 141,379,660-141,379,669 GNPDA1
    nsv5087122mobile element insertion1nstd203human GRCh38 chr5: 142,000,104-142,000,104 , GRCh37.p13 chr5: 141,379,669-141,379,669 GNPDA1
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