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Items: 1 to 20 of 150

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7097553copy number variation1nstd102humanPathogenic GRCh37 chr5: 94,800,311-96,107,383 , GRCh38.p12 chr5: 95,464,607-96,771,679 LOC105379675, GPR150, 27 more genes
    nsv7097303copy number variation1nstd102humanPathogenic GRCh37 chr5: 95,998,127-96,107,383 , GRCh38.p12 chr5: 96,662,423-96,771,679 CAST, ERAP1, 1 more genes
    nsv7058036inversion1nstd229human GRCh38 chr5: 94,195,543-97,660,538 , GRCh37.p13 chr5: 93,531,248-96,996,242 RIOK2, SPATA9, 51 more genes
    nsv7055396inversion1nstd229human GRCh38 chr5: 96,167,047-97,983,533 , GRCh37.p13 chr5: 95,502,751-97,319,237 MTCYBP40, LINC02234, 22 more genes
    nsv7044198inversion1nstd229human GRCh38 chr5: 93,856,097-99,790,151 , GRCh37.p13 chr5: 93,191,803-99,125,855 FAM81B, LOC107986365, 78 more genes
    nsv6773004copy number variation1nstd229human GRCh38 chr5: 94,767,305-97,708,544 , GRCh37.p13 chr5: 94,103,010-97,044,248 FABP5P5, SPATA9, 45 more genes
    nsv6772411copy number variation1nstd229human GRCh38 chr5: 96,306,242-96,783,194 , GRCh37.p13 chr5: 95,641,946-96,118,898 CAST, LOC107986363, 5 more genes
    nsv6772251copy number variation1nstd229human GRCh38 chr5: 96,326,801-96,820,500 , GRCh37.p13 chr5: 95,662,505-96,156,203 CAST, PCSK1, 5 more genes
    nsv6768538copy number variation1nstd229human GRCh38 chr5: 96,650,784-96,744,561 , GRCh37.p13 chr5: 95,986,488-96,080,265 CAST, LOC107986363
    nsv6764992copy number variation1nstd229human GRCh38 chr5: 96,713,419-96,724,472 , GRCh37.p13 chr5: 96,049,123-96,060,176 CAST, LOC107986363
    nsv6763717copy number variation1nstd229human GRCh38 chr5: 96,412,203-97,185,198 , GRCh37.p13 chr5: 95,747,907-96,520,902 RPS20P16, PCSK1, 12 more genes
    nsv6561301inversion1nstd223human GRCh38 chr5: 96,713,162-96,713,697 , GRCh37.p13 chr5: 96,048,866-96,049,401 LOC107986363, CAST
    nsv6557580inversion1nstd223human GRCh38 chr5: 96,713,135-96,713,698 , GRCh37.p13 chr5: 96,048,839-96,049,402 LOC107986363, CAST
    nsv6410604copy number variation1nstd223human GRCh38 chr5: 96,650,762-96,744,663 , GRCh37.p13 chr5: 95,986,466-96,080,367 CAST, LOC107986363
    nsv6405214copy number variation1nstd223human GRCh38 chr5: 96,387,085-97,100,180 , GRCh37.p13 chr5: 95,722,789-96,435,884 RPS20P16, CAST, 10 more genes
    nsv6402193copy number variation1nstd223human GRCh38 chr5: 96,306,242-96,783,190 , GRCh37.p13 chr5: 95,641,946-96,118,894 CAST, PCSK1, 5 more genes
    nsv6313580copy number variation1nstd102humanPathogenic GRCh37 chr5: 93,650,000-114,969,108 , GRCh38.p12 chr5: 94,314,295-115,633,411 FER, HMGN1P15, 222 more genes
    nsv6137154translocation1nstd213human GRCh37 chr5: 96,043,857-96,043,857 , GRCh37 chr5: 112,454,509-112,454,509 , GRCh38.p12 chr5: 96,708,153-96,708,153 , GRCh38.p12 chr5: 113,118,812-113,118,812 CAST, MCC, 1 more genes
    nsv6135688copy number variation1nstd213human GRCh37 chr5: 95,520,000-96,660,001 , GRCh38.p12 chr5: 96,184,296-97,324,297 RNU6-524P, RNU1-73P, 15 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
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