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Items: 1 to 20 of 102

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7099187copy number variation1nstd231human GRCh38.p12 chr1: 24,354,009-27,158,528 , GRCh37 chr1: 24,680,499-27,485,019 RUNX3, CD52, 88 more genes
    nsv7095609copy number variation1nstd102humanUncertain significance GRCh37 chr1: 25,870,190-27,278,871 , GRCh38.p12 chr1: 25,543,699-26,952,380 RPL34P4, GPATCH3, 53 more genes
    nsv7046473inversion1nstd229human GRCh38 chr1: 26,763,482-26,955,083 , GRCh37.p13 chr1: 27,089,973-27,281,574 GPATCH3, RN7SL165P, 8 more genes
    nsv7044103inversion1nstd229human GRCh38 chr1: 26,905,652-33,050,814 , GRCh37.p13 chr1: 27,232,143-33,516,415 ADGRB2, SNORA16A, 169 more genes
    nsv6648045copy number variation1nstd229human GRCh38 chr1: 26,400,001-27,138,900 , GRCh37.p13 chr1: 26,726,492-27,465,391 RN7SL679P, NR0B2, 26 more genes
    nsv6648009copy number variation1nstd229human GRCh38 chr1: 26,787,530-27,211,044 , GRCh37.p13 chr1: 27,114,021-27,537,535 RPL18AP5, RN7SL165P, 19 more genes
    nsv6647354copy number variation1nstd229human GRCh38 chr1: 26,095,901-27,680,900 , GRCh37.p13 chr1: 26,422,392-28,007,411 ZPLD2P, CEP85, 65 more genes
    nsv6647254copy number variation1nstd229human GRCh38 chr1: 21,562,611-27,513,090 , GRCh37.p13 chr1: 21,889,104-27,839,601 RPL18AP5, LINC00339, 184 more genes
    nsv6647227copy number variation1nstd229human GRCh38 chr1: 20,848,934-27,947,465 , GRCh37.p13 chr1: 21,175,427-28,273,976 RPL17P9, ALPL, 218 more genes
    nsv6333556copy number variation1nstd223human GRCh38 chr1: 24,890,501-27,921,300 , GRCh37.p13 chr1: 25,216,992-28,247,811 RUNX3, MACO1, 108 more genes
    nsv6310806copy number variation1nstd102humanUncertain significance GRCh37 chr1: 27,117,307-27,480,825 , GRCh38.p12 chr1: 26,790,816-27,154,334 RPL32P6, TRNP1, 14 more genes
    nsv6133648copy number variation1nstd213human GRCh37 chr1: 23,300,000-28,930,001 , GRCh38.p12 chr1: 22,973,507-28,603,489 RUNX3, CD52, 195 more genes
    nsv5880550copy number variation1nstd209human GRCh38 chr1: 26,908,300-26,914,211 , GRCh37.p13 chr1: 27,234,791-27,240,702 NUDC, NR0B2
    nsv5829935copy number variation1nstd209human GRCh38 chr1: 26,908,332-26,914,231 , GRCh37.p13 chr1: 27,234,823-27,240,722 NR0B2, NUDC
    nsv5829672copy number variation1nstd209human GRCh38 chr1: 26,912,532-26,913,531 , GRCh37.p13 chr1: 27,239,023-27,240,022 NUDC, NR0B2
    nsv5430614copy number variation1nstd206human GRCh38 chr1: 26,905,252-26,918,611 , GRCh37.p13 chr1: 27,231,743-27,245,102 NUDC, NR0B2
    nsv5427686copy number variation1nstd206human GRCh38 chr1: 22,064,395-28,290,354 , GRCh37.p13 chr1: 22,390,888-28,616,865 , NCMAP-DT, 201 more genes
    nsv5344677translocation1nstd200human GRCh37 chr1: 27,238,541-27,238,541 , GRCh37 chr1: 27,238,444-27,238,444 , GRCh38.p12 chr1: 26,911,953-26,911,953 , GRCh38.p12 chr1: 26,912,050-26,912,050 NR0B2, NUDC
    nsv5206193copy number variation1nstd204human GRCh38.p13 chr1: 26,819,201-27,230,300 , GRCh37.p13 chr1: 27,145,692-27,556,791 KDF1, RPL12P13, 18 more genes
    nsv5068307mobile element insertion1nstd203human GRCh38 chr1: 26,912,266-26,912,282 , GRCh37.p13 chr1: 27,238,757-27,238,773 NUDC, NR0B2
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