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Items: 1 to 20 of 122

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    esv3106596copy number variation1estd209human GRCh37 chr7: 129,408,456-129,408,457 , GRCh38.p12 chr7: 129,768,616-129,768,617 LOC105375501, MIR182
    esv1276265copy number variation1estd22human NCBI36 chr7: 129,195,709-129,195,710 , GRCh37.p13 chr7: 129,408,473-129,408,474 , GRCh38.p12 chr7: 129,768,633-129,768,634 LOC105375501, MIR182
    nsv2529915short tandem repeat2nstd128human GRCh37 chr7: 129,409,308-129,409,324 , GRCh38.p12 chr7: 129,769,468-129,769,484 MIR182, LOC105375501
    nsv3892293copy number variation1nstd102humanBenign GRCh37 chr7: 129,404,661-129,414,161 , GRCh38.p12 chr7: 129,764,821-129,774,321 MIR182, MIR183, 2 more genes
    nsv4958298copy number variation1nstd200human GRCh38 chr7: 129,767,261-129,776,885 , GRCh37.p13 chr7: 129,407,101-129,416,725 MIR182, MIR96, 2 more genes
    nsv949946copy number variation1nstd73human GRCh37 chr7: 129,402,801-129,450,400 , GRCh38.p12 chr7: 129,762,961-129,810,560 MIR182, MIR183, 2 more genes
    nsv608420copy number variation1nstd54human NCBI36 chr7: 129,184,880-129,232,187 , GRCh37.p13 chr7: 129,397,644-129,444,951 , GRCh38.p12 chr7: 129,757,804-129,805,111 MIR182, LOC105375501, 2 more genes
    nsv464721copy number variation1nstd27human NCBI35 chr7: 128,991,595-129,038,902 , GRCh37.p13 chr7: 129,397,644-129,444,951 , GRCh38.p12 chr7: 129,757,804-129,805,111 MIR96, MIR182, 2 more genes
    nsv5487017copy number variation1nstd206human GRCh38 chr7: 129,744,293-129,771,997 , GRCh37.p13 chr7: 129,384,133-129,411,837 NRF1, MIR182, 2 more genes
    nsv6304199copy number variation1nstd186human GRCh37 chr7: 129,384,133-129,411,837 , GRCh38.p12 chr7: 129,744,293-129,771,997 NRF1, MIR182, 2 more genes
    esv3851377copy number variation1estd219human GRCh37 chr7: 129,383,971-129,411,481 , GRCh38.p12 chr7: 129,744,131-129,771,641 MIR182, NRF1, 2 more genes
    esv3615005copy number variation1estd214human GRCh37 chr7: 129,383,971-129,411,481 , GRCh38.p12 chr7: 129,744,131-129,771,641 MIR182, LOC105375501, 2 more genes
    esv1843969copy number variation1estd188human NCBI36 chr7: 129,190,777-129,233,834 , GRCh37.p13 chr7: 129,403,541-129,446,598 , GRCh38.p12 chr7: 129,763,701-129,806,758 MIR96, LOC105375501, 2 more genes
    esv1802311copy number variation1estd188human NCBI36 chr7: 129,194,172-129,229,625 , GRCh37.p13 chr7: 129,406,936-129,442,389 , GRCh38.p12 chr7: 129,767,096-129,802,549 LOC105375501, MIR182, 2 more genes
    esv1828133copy number variation1estd188human NCBI36 chr7: 129,190,777-129,224,349 , GRCh37.p13 chr7: 129,403,541-129,437,113 , GRCh38.p12 chr7: 129,763,701-129,797,273 LOC105375501, MIR96, 2 more genes
    esv1808977copy number variation1estd188human NCBI36 chr7: 129,189,394-129,211,697 , GRCh37.p13 chr7: 129,402,158-129,424,461 , GRCh38.p12 chr7: 129,762,318-129,784,621 LOC105375501, MIR96, 2 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 RNU6-438P, LOC105375300, 2682 more genes
    nsv3888815copy number variation1nstd102humanPathogenic GRCh37 chr7: 12,258,147-140,494,267 , GRCh38.p12 chr7: 12,218,521-140,794,467 LOC107986817, DNAJB9, 2014 more genes
    nsv3916726copy number variation1nstd102humanPathogenic NCBI36 chr7: 116,754,095-134,125,980 , GRCh38 chr7: 117,326,805-134,790,689 , GRCh37 chr7: 116,966,859-134,475,440 LOC107986845, TPI1P2, 245 more genes
    nsv3903275copy number variation1nstd102humanPathogenic GRCh37 chr7: 127,295,698-139,524,358 , GRCh38.p12 chr7: 127,655,644-139,824,559 RNU6-1272P, KCP, 224 more genes
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