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Items: 1 to 20 of 126

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7055634inversion1nstd229human GRCh38 chr4: 152,515,897-153,221,494 , GRCh37.p13 chr4: 153,437,049-154,142,646 MIR4453, NSA2P6, 12 more genes
    nsv7048230inversion1nstd229human GRCh38 chr4: 149,781,104-157,324,460 , GRCh37.p13 chr4: 150,702,256-158,245,612 LOC107986197, LINC02273, 119 more genes
    nsv7046905inversion1nstd229human GRCh38 chr4: 151,269,540-154,434,057 , GRCh37.p13 chr4: 152,190,692-155,355,209 GATB, LOC105377492, 47 more genes
    nsv6756598copy number variation1nstd229human GRCh38 chr4: 152,493,101-152,847,600 , GRCh37.p13 chr4: 153,414,253-153,768,752 TMEM154, TIGD4, 8 more genes
    nsv6755685copy number variation1nstd229human GRCh38 chr4: 152,442,701-152,859,600 , GRCh37.p13 chr4: 153,363,853-153,780,752 ARFIP1, FBXW7, 9 more genes
    nsv6751319copy number variation1nstd229human GRCh38 chr4: 152,441,580-152,564,339 , GRCh37.p13 chr4: 153,362,732-153,485,491 RPS3AP18, MIR4453HG, 3 more genes
    nsv6750744copy number variation1nstd229human GRCh38 chr4: 152,532,701-152,537,100 , GRCh37.p13 chr4: 153,453,853-153,458,252 MIR4453, FBXW7, 1 more genes
    nsv6629560copy number variation1nstd224human GRCh37 chr4: 153,419,508-154,214,200 , GRCh38.p12 chr4: 152,498,356-153,293,048 FBXW7, FAM192BP, 14 more genes
    nsv6572617inversion1nstd223human GRCh38 chr4: 151,269,541-154,434,055 , GRCh37.p13 chr4: 152,190,693-155,355,207 LOC107986197, LOC100419170, 47 more genes
    nsv6135297copy number variation1nstd213human GRCh37 chr4: 148,450,000-155,050,001 , GRCh38.p12 chr4: 147,528,848-154,128,849 ANXA2P1, ASS1P8, 86 more genes
    nsv6134911copy number variation1nstd213human GRCh37 chr4: 147,270,000-190,610,001 , GRCh38.p12 chr4: 146,348,848-189,688,847 , AGA, 517 more genes
    nsv6134884copy number variation1nstd213human GRCh37 chr4: 109,230,000-161,720,001 , GRCh38.p12 chr4: 108,308,844-160,798,849 , ANK2, 616 more genes
    nsv6134731copy number variation1nstd213human GRCh37 chr4: 109,230,000-161,710,001 , GRCh38.p12 chr4: 108,308,844-160,788,849 , ANK2, 616 more genes
    nsv6112754copy number variation1nstd102humanPathogenic GRCh37 chr4: 131,303,317-168,722,402 , GRCh38.p12 chr4: 130,382,162-167,801,251 MIR3139, CLGN, 407 more genes
    nsv5562145sequence alteration1nstd206human GRCh38 chr4: 74,717,205-184,730,527 , GRCh37.p13 chr4: 75,689,880-185,651,681 , ASS1P8, 1307 more genes
    nsv5033844inversion1nstd200human GRCh38 chr4: 151,269,541-154,434,055 , GRCh37.p13 chr4: 152,190,693-155,355,207 RNU6-1282P, RNF175, 47 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
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