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Items: 1 to 20 of 131

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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
    nsv5468408copy number variation1nstd206human GRCh38 chr4: 119,303,930-119,328,528 , GRCh37.p13 chr4: 120,225,085-120,249,683 C4orf3, FABP2
    nsv5381774copy number variation1nstd102humanPathogenic GRCh37 chr4: 116,833,638-130,232,122 , GRCh38.p12 chr4: 115,912,482-129,310,967 LOC112268469, LOC105377393, 159 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
    nsv4680924copy number variation1nstd189human GRCh37.p13 chr4: 119,927,966-120,308,980 , GRCh38.p12 chr4: 119,006,811-119,387,825 FABP2, MYOZ2, 10 more genes
    nsv4674606copy number variation1nstd102humanUncertain significance GRCh37 chr4: 120,191,740-120,248,879 , GRCh38.p12 chr4: 119,270,585-119,327,724 USP53, C4orf3, 1 more genes
    nsv4436254copy number variation1nstd102humanLikely pathogenic GRCh37 chr4: 116,624,547-126,168,646 , GRCh38.p12 chr4: 115,703,391-125,247,491 ANXA5, CCNA2, 125 more genes
    nsv4342697sequence alteration1nstd166human GRCh37.p13 chr4: 73,901,505-160,870,682 , GRCh38.p12 chr4: 73,035,788-159,949,530 , ADH1B, 1083 more genes
    nsv4104766copy number variation1nstd166human GRCh37.p13 chr4: 120,224,534-120,322,126 , GRCh38.p12 chr4: 119,303,379-119,400,971 FABP2, GK6P, 4 more genes
    nsv3924008copy number variation1nstd102humanPathogenic GRCh38 chr4: 118,065,569-190,042,639 , GRCh37 chr4: 118,986,724-190,828,225 , NCBI36 chr4: 119,206,172-191,200,788 PPID, METTL14-DT, 828 more genes
    nsv3922957copy number variation1nstd102humanPathogenic GRCh37 chr4: 118,273,037-134,486,822 , GRCh38 chr4: 117,351,881-133,565,667 , NCBI36 chr4: 118,492,485-134,706,272 LOC102724158, LOC105377411, 168 more genes
    nsv3920388copy number variation1nstd102humanPathogenic GRCh37 chr4: 97,014,044-137,331,362 , NCBI36 chr4: 97,233,067-137,550,812 , GRCh38 chr4: 96,092,893-136,410,207 MIR576, ABT1P1, 447 more genes
    nsv3918438copy number variation1nstd102humanLikely benign GRCh38 chr4: 118,858,868-119,856,165 , GRCh37 chr4: 119,780,023-120,777,320 , NCBI36 chr4: 119,999,471-120,996,768 LINC01365, LOC107986192, 23 more genes
    nsv3917126copy number variation1nstd102humanPathogenic GRCh38 chr4: 116,630,862-145,429,900 , NCBI36 chr4: 117,771,466-146,570,502 , GRCh37 chr4: 117,552,018-146,351,052 SETD7, HSPD1P5, 294 more genes
    nsv3916316copy number variation1nstd102humanUncertain significance NCBI36 chr4: 111,318,515-191,263,063 , GRCh37.p13 chr4: 111,099,066-191,029,082 , GRCh38.p12 chr4: 110,177,910-190,107,927 RNU7-194P, FOSL1P1, 939 more genes
    nsv3912397copy number variation1nstd102humanUncertain significance NCBI36 chr4: 117,231,601-120,685,768 , GRCh37.p13 chr4: 117,012,152-120,466,320 , GRCh38.p12 chr4: 116,090,996-119,545,165 MIR1973, PRSS12, 60 more genes
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