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Items: 1 to 20 of 45

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6312415copy number variation1nstd102humanPathogenic GRCh38 chr7: 44,145,167-44,145,585 , GRCh37 chr7: 44,184,766-44,185,184 GCK
    nsv7148044copy number variation1nstd102humanLikely pathogenic GRCh37 chr7: 44,185,084-44,185,085 , GRCh38 chr7: 44,145,485-44,145,486 GCK
    nsv7137155delins1nstd102humanLikely pathogenic GRCh37 chr7: 44,184,608-44,184,775 , GRCh38 chr7: 44,145,009-44,145,176 GCK
    nsv3888989copy number variation1nstd102humanPathogenic GRCh37 chr11: 64,570,986-64,577,604 , GRCh38 chr11: 64,803,514-64,810,132 MEN1, MAP4K2
    nsv3882253copy number variation1nstd102humanPathogenic GRCh37 chr11: 64,570,986-64,572,288 , GRCh38 chr11: 64,803,514-64,804,816 MEN1, MAP4K2
    nsv3878800copy number variation1nstd102humanPathogenic GRCh37 chr11: 64,570,986-64,572,288 , GRCh38 chr11: 64,803,514-64,804,816 MEN1, MAP4K2
    nsv1397900copy number variation1nstd45humanPathogenic GRCh37 chr11: 64,570,986-64,578,766 , GRCh38.p12 chr11: 64,803,514-64,811,294 MEN1, MAP4K2
    nsv3894851copy number variation1nstd102humanBenign GRCh37 chr11: 64,544,135-64,622,868 , GRCh38.p12 chr11: 64,776,663-64,855,396 MEN1, SF1, 3 more genes
    nsv3919826copy number variation1nstd102humanPathogenic GRCh37 chr7: 54,185-159,075,079 , GRCh38 chr7: 54,185-159,282,390 , NCBI36 chr7: 149,268-158,767,840 GCK, RNU6-438P, 2682 more genes
    nsv3888815copy number variation1nstd102humanPathogenic GRCh37 chr7: 12,258,147-140,494,267 , GRCh38.p12 chr7: 12,218,521-140,794,467 GCK, LOC107986817, 2014 more genes
    nsv5380796copy number variation1nstd102humanPathogenic GRCh37 chr11: 11,835,569-118,373,112 , GRCh38.p12 chr11: 11,814,022-118,502,397 FAUP4, MMP7, 2031 more genes
    nsv3924054copy number variation1nstd102humanPathogenic GRCh37 chr7: 40,573,756-56,174,815 , NCBI36 chr7: 40,540,281-56,142,309 , GRCh38 chr7: 40,534,157-56,107,122 GCK, VOPP1-DT, 229 more genes
    nsv3897424copy number variation1nstd102humanPathogenic GRCh37 chr7: 32,911,003-44,576,005 , GRCh38.p12 chr7: 32,871,391-44,536,406 GCK, LOC107986734, 192 more genes
    nsv3916442copy number variation1nstd102humanPathogenic NCBI36 chr7: 37,309,607-48,670,880 , GRCh37 chr7: 37,343,082-48,700,334 , GRCh38 chr7: 37,303,478-48,660,738 GCK, LOC102724903, 204 more genes
    nsv3911166copy number variation1nstd102humanPathogenic GRCh37 chr7: 40,060,197-50,611,198 , NCBI36 chr7: 40,026,722-50,578,692 , GRCh38 chr7: 40,020,598-50,543,500 GCK, SUGCT, 155 more genes
    nsv6313509copy number variation1nstd102humanPathogenic GRCh37 chr7: 40,778,439-50,228,656 , GRCh38.p12 chr7: 40,738,840-50,189,060 GCK, LINC01447, 142 more genes
    nsv3924742copy number variation1nstd102humanPathogenic GRCh37 chr7: 38,217,601-45,343,699 , GRCh38 chr7: 38,177,999-45,304,100 , NCBI36 chr7: 38,184,126-45,310,224 GCK, NUDCD3, 152 more genes
    nsv5381787copy number variation1nstd102humanPathogenic GRCh37 chr7: 43,341,583-50,171,623 , GRCh38.p12 chr7: 43,301,984-50,132,027 GCK, OGDH, 110 more genes
    nsv5381783copy number variation1nstd102humanPathogenic GRCh37 chr7: 41,124,364-47,945,566 , GRCh38.p12 chr7: 41,084,766-47,905,969 GCK, ELK1P1, 121 more genes
    nsv3896166copy number variation1nstd102humanPathogenic GRCh37 chr7: 40,350,383-47,034,422 , GRCh38.p12 chr7: 40,310,784-46,994,824 GCK, LOC112267984, 118 more genes
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