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Items: 1 to 20 of 127

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6795912copy number variation1nstd229human GRCh38 chr6: 24,928,620-25,319,577 , GRCh37.p13 chr6: 24,928,848-25,319,805 LOC105374981, RIPOR2, 15 more genes
    nsv6794563copy number variation1nstd229human GRCh38 chr6: 25,006,402-25,023,540 , GRCh37.p13 chr6: 25,006,630-25,023,768 ASS1P1, RIPOR2, 1 more genes
    nsv6788753copy number variation1nstd229human GRCh38 chr6: 24,741,133-25,156,893 , GRCh37.p13 chr6: 24,741,361-25,157,121 NUP50P2, ASS1P1, 12 more genes
    nsv6780503copy number variation1nstd229human GRCh38 chr6: 24,992,543-25,017,921 , GRCh37.p13 chr6: 24,992,771-25,018,149 LOC102724765, RIPOR2
    nsv6574272inversion1nstd223human GRCh38 chr6: 25,019,734-25,021,033 , GRCh37.p13 chr6: 25,019,962-25,021,261 RIPOR2, ASS1P1, 1 more genes
    nsv6015558copy number variation1nstd212human GRCh38 chr6: 25,031,729-25,031,783 , GRCh37.p13 chr6: 25,031,957-25,032,011 RIPOR2, LOC102724765, 1 more genes
    nsv5578533copy number variation1nstd207human GRCh38 chr6: 25,031,733-25,031,782 , GRCh37.p13 chr6: 25,031,961-25,032,010 RIPOR2, LOC102724765, 1 more genes
    nsv5100378mobile element insertion1nstd203human GRCh38 chr6: 25,032,306-25,032,321 , GRCh37.p13 chr6: 25,032,534-25,032,549 LOC102724765, RIPOR2
    nsv4933208copy number variation1nstd200human GRCh38 chr6: 25,036,346-25,037,386 , GRCh37.p13 chr6: 25,036,574-25,037,614 RIPOR2, LOC102724765
    nsv4740283copy number variation1nstd199human GRCh38.p12 chr6: 25,031,729-25,031,784 , GRCh37 chr6: 25,031,957-25,032,012 RIPOR2, LOC102724765, 1 more genes
    nsv4675407copy number variation1nstd102humanUncertain significance GRCh37 chr6: 24,497,678-25,168,510 , GRCh38.p12 chr6: 24,497,450-25,168,282 C6orf62, AP3S1P1, 18 more genes
    nsv4645897copy number variation1nstd186human GRCh37 chr6: 25,031,957-25,032,011 , GRCh38.p12 chr6: 25,031,729-25,031,783 RIPOR2, LOC102724765, 1 more genes
    nsv4122985copy number variation1nstd166human GRCh37.p13 chr6: 25,031,957-25,032,011 , GRCh38.p12 chr6: 25,031,729-25,031,783 RIPOR2, RN7SL334P, 1 more genes
    nsv3922819copy number variation1nstd102humanUncertain significance NCBI36 chr6: 23,360,729-26,075,484 , GRCh37 chr6: 23,252,750-25,967,505 , GRCh38 chr6: 23,252,522-25,967,277 KAAG1, ACOT13, 52 more genes
    nsv3922675copy number variation1nstd102humanPathogenic GRCh37 chr6: 22,519,683-25,226,559 , NCBI36 chr6: 22,627,662-25,334,538 , GRCh38 chr6: 22,519,454-25,226,331 PPIAP29, ACOT13, 42 more genes
    nsv3920564copy number variation1nstd102humanPathogenic GRCh38 chr6: 3,224,310-30,657,190 , GRCh37 chr6: 3,224,544-30,624,967 , NCBI36 chr6: 3,169,543-30,732,946 PRELID1P2, RPL7AP7, 785 more genes
    nsv3913920copy number variation1nstd102humanPathogenic GRCh38 chr6: 156,974-46,789,291 , NCBI36 chr6: 101,974-46,864,987 , GRCh37 chr6: 156,974-46,757,028 TRR-ACG1-2, TMEM217, 1385 more genes
    nsv3889814copy number variation1nstd102humanPathogenic GRCh37 chr6: 165,632-170,919,470 , GRCh38.p12 chr6: 165,632-170,610,382 ITPR3, HSD17B8, 2905 more genes
    nsv3887898copy number variation2nstd102humanPathogenic GRCh37 chr6: 156,975-170,919,482 , GRCh38.p12 chr6: 156,975-170,610,394 SOD1P1, HLA-DPB1, 2905 more genes
    nsv3879811copy number variation1nstd102humanPathogenic GRCh37 chr6: 108,666-170,980,171 , GRCh38.p12 chr6: 108,666-170,671,083 RNU6-411P, LOC107986611, 2910 more genes
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