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Items: 1 to 20 of 154

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5562145sequence alteration1nstd206human GRCh38 chr4: 74,717,205-184,730,527 , GRCh37.p13 chr4: 75,689,880-185,651,681 , ASS1P8, 1307 more genes
    nsv5547030insertion1nstd206human GRCh38 chr4: 68,996,170-113,894,177 , GRCh37.p13 chr4: 69,861,888-114,815,333 , MIR548AH, 616 more genes
    nsv5311950copy number variation1nstd204human GRCh38.p13 chr4: 82,566,868-82,637,571 , GRCh37.p13 chr4: 83,488,021-83,558,724 PTPN11P5, SCD5, 1 more genes
    nsv5225907copy number variation1nstd204human GRCh38.p13 chr4: 82,566,034-82,595,593 , GRCh37.p13 chr4: 83,487,187-83,516,746 PTPN11P5
    nsv5224172copy number variation1nstd204human GRCh38.p13 chr4: 82,566,784-82,583,621 , GRCh37.p13 chr4: 83,487,937-83,504,774 PTPN11P5
    nsv5040446inversion1nstd200human GRCh38 chr4: 76,223,829-89,968,114 , GRCh37.p13 chr4: 77,144,982-90,889,265 , KPNA2P1, 209 more genes
    nsv5037291inversion1nstd200human GRCh38 chr4: 74,160,096-84,998,626 , GRCh37.p13 chr4: 75,025,813-85,919,779 , LOC105377302, 175 more genes
    nsv5034204inversion1nstd200human GRCh38 chr4: 45,103,677-117,623,076 , GRCh37.p13 chr4: 45,105,694-118,544,231 , LOC100129728, 913 more genes
    nsv4923292copy number variation1nstd200human GRCh38 chr4: 82,570,221-82,585,572 , GRCh37.p13 chr4: 83,491,374-83,506,725 PTPN11P5
    nsv4878267inversion1nstd200human GRCh37 chr4: 45,105,694-118,544,231 , GRCh38.p12 chr4: 45,103,677-117,623,076 , MIR367, 913 more genes
    nsv4809341copy number variation1nstd200human GRCh37 chr4: 83,488,045-83,558,701 , GRCh38.p12 chr4: 82,566,892-82,637,548 LINC00575, PTPN11P5, 1 more genes
    nsv4761770inversion1nstd199human GRCh37 chr4: 34,988-191,015,248 , GRCh38.p12 chr4: 34,988-190,094,093 , ADD1, 2433 more genes
    nsv4758212inversion1nstd199human GRCh37 chr4: 30,775-191,019,445 , GRCh38.p12 chr4: 30,775-190,098,290 , ADD1, 2433 more genes
    nsv4754592inversion1nstd199human GRCh37 chr4: 27,111-191,020,337 , GRCh38.p12 chr4: 27,111-190,099,182 , ADD1, 2433 more genes
    nsv4753570inversion1nstd199human GRCh37 chr4: 19,034-191,028,414 , GRCh38.p12 chr4: 19,034-190,107,259 , ADD1, 2434 more genes
    nsv4751554inversion1nstd199human GRCh37 chr4: 18,939-191,034,785 , GRCh38.p12 chr4: 18,939-190,113,630 , ADD1, 2434 more genes
    nsv4729598copy number variation1nstd102humanPathogenic GRCh37 chr4: 71,412,409-87,920,784 , GRCh38.p12 chr4: 70,546,692-86,999,632 PTPN11P5, LOC643014, 244 more genes
    nsv4684176copy number variation1nstd102humanPathogenic GRCh37 chr4: 83,196,931-85,540,706 , GRCh38.p12 chr4: 82,275,778-84,619,553 VAMP9P, SNORD144, 43 more genes
    nsv4674589copy number variation1nstd102humanPathogenic GRCh37 chr4: 72,680,879-86,426,232 , GRCh38.p12 chr4: 71,815,162-85,505,079 SOWAHB, FTLP9, 211 more genes
    nsv4674457copy number variation1nstd102humanPathogenic GRCh37 chr4: 82,593,140-85,651,685 , GRCh38.p12 chr4: 81,671,986-84,730,532 RPL7AP26, TMEM150C, 50 more genes
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