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Items: 1 to 20 of 113

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6787290copy number variation1nstd229human GRCh38 chr6: 25,240,953-26,330,257 , GRCh37.p13 chr6: 25,241,181-26,330,485 CARMIL1, H2AC8, 74 more genes
    nsv6785917copy number variation1nstd229human GRCh38 chr6: 25,619,649-25,744,363 , GRCh37.p13 chr6: 25,619,877-25,744,591 H2BC1, PRELID1P2, 6 more genes
    nsv6783968copy number variation1nstd229human GRCh38 chr6: 25,284,234-25,728,953 , GRCh37.p13 chr6: 25,284,462-25,729,181 RNU6-987P, H2BC1, 5 more genes
    nsv6573780inversion1nstd223human GRCh38 chr6: 25,727,503-25,727,757 , GRCh37.p13 chr6: 25,727,731-25,727,985 SLC17A1, H2BC1
    nsv6402318copy number variation1nstd223human GRCh38 chr6: 25,240,953-26,330,257 , GRCh37.p13 chr6: 25,241,181-26,330,485 H2BC7, H2AC7, 74 more genes
    nsv5301217copy number variation1nstd204human GRCh37.p13 chr6: 25,724,633-25,728,969 , GRCh38.p13 chr6: 25,724,405-25,728,741 SLC17A1, H2AC1, 1 more genes
    nsv5232451copy number variation1nstd204human GRCh38.p13 chr6: 25,726,399-25,727,498 , GRCh37.p13 chr6: 25,726,627-25,727,726 H2BC1, SLC17A1, 1 more genes
    nsv5222324copy number variation1nstd204human GRCh38.p13 chr6: 25,724,099-25,728,998 , GRCh37.p13 chr6: 25,724,327-25,729,226 H2BC1, SLC17A1, 1 more genes
    nsv4934532copy number variation1nstd200human GRCh38 chr6: 25,619,649-25,744,363 , GRCh37.p13 chr6: 25,619,877-25,744,591 SCGN, H2BC2P, 6 more genes
    nsv4729301copy number variation1nstd102humanUncertain significance GRCh37 chr6: 25,622,751-25,853,825 , GRCh38.p12 chr6: 25,622,523-25,853,597 H2AC1, SLC17A4, 7 more genes
    nsv4598435copy number variation1nstd183human GRCh37 chr6: 25,589,165-25,820,124 , GRCh38.p12 chr6: 25,588,937-25,819,896 SLC17A1, SLC17A4, 7 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
    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
    nsv3877040copy number variation1nstd102humanPathogenic GRCh37 chr6: 60,107-171,054,786 , GRCh38.p12 chr6: 60,107-170,745,698 LOC105378061, MIR4640, 2914 more genes
    nsv3169066inversion1nstd158human GRCh37 chr6: 5,923,377-99,717,885 , GRCh38.p12 chr6: 5,923,144-99,270,009 , ABCF1, 1877 more genes
    nsv3168939inversion1nstd158human GRCh37 chr6: 12,268,690-80,058,596 , GRCh38.p12 chr6: 12,268,457-79,348,879 , ABCF1, 1548 more genes
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