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Items: 1 to 20 of 37

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3913055copy number variation1nstd102humanUncertain significance GRCh38 chr7: 131,228,764-131,452,396 , GRCh37 chr7: 130,913,523-131,137,155 , NCBI36 chr7: 130,564,063-130,787,695 MKLN1, RPL27P11, 1 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 MKLN1, 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 MKLN1, LOC107986817, 2014 more genes
    nsv7097864copy number variation1nstd102humanPathogenic GRCh37 chr7: 130,781,014-150,301,047 , GRCh38.p12 chr7: 131,096,255-150,603,959 MKLN1, NOBOX, 466 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 MKLN1, LOC107986845, 245 more genes
    nsv3903275copy number variation1nstd102humanPathogenic GRCh37 chr7: 127,295,698-139,524,358 , GRCh38.p12 chr7: 127,655,644-139,824,559 MKLN1, RNU6-1272P, 224 more genes
    nsv6313876copy number variation1nstd102humanPathogenic GRCh37 chr7: 124,103,982-134,693,590 , GRCh38.p12 chr7: 124,463,928-135,008,839 MKLN1, IMPDH1, 174 more genes
    nsv3910648copy number variation1nstd102humanPathogenic GRCh38 chr7: 124,170,657-134,163,594 , GRCh37 chr7: 123,810,711-133,848,346 , NCBI36 chr7: 123,597,947-133,498,886 MKLN1, CPA1, 165 more genes
    nsv6313722copy number variation1nstd102humanPathogenic GRCh37 chr7: 123,967,475-132,729,981 , GRCh38.p12 chr7: 124,327,421-133,045,221 MKLN1, IRF5, 153 more genes
    nsv3915522copy number variation1nstd102humanPathogenic GRCh38 chr7: 126,859,732-132,750,936 , NCBI36 chr7: 126,287,022-132,086,236 , GRCh37 chr7: 126,499,786-132,435,696 MKLN1, LRRC4, 126 more genes
    nsv3894780copy number variation1nstd102humanPathogenic GRCh37 chr7: 10,704-159,122,532 , GRCh38.p12 chr7: 10,704-159,329,842 MKLN1, RNU6-565P, 2684 more genes
    nsv4455091copy number variation1nstd102humanPathogenic GRCh37 chr7: 10,365-159,119,707 , GRCh38.p12 chr7: 10,365-159,327,017 MKLN1, RPL23AP51, 2684 more genes
    nsv3909087copy number variation1nstd102humanPathogenic GRCh37 chr7: 44,935-159,126,310 , GRCh38.p12 chr7: 44,935-159,333,620 MKLN1, MNX1-AS2, 2682 more genes
    nsv3908592copy number variation2nstd102humanPathogenic GRCh37 chr7: 43,361-159,119,707 , GRCh38.p12 chr7: 43,361-159,327,017 MKLN1, TRGV3, 2682 more genes
    nsv3922815copy number variation1nstd102humanPathogenic NCBI36 chr7: 96,887,100-158,409,214 , GRCh38 chr7: 97,419,852-158,923,762 , GRCh37 chr7: 97,049,164-158,716,453 MKLN1, SEPTIN7P6, 1175 more genes
    nsv3894097copy number variation1nstd102humanPathogenic GRCh37 chr7: 98,693,388-159,119,707 , GRCh38.p12 chr7: 99,095,765-159,327,017 MKLN1, CYP3A5, 1144 more genes
    nsv4675620copy number variation1nstd102humanPathogenic GRCh37 chr7: 109,251,060-159,119,707 , GRCh38.p12 chr7: 109,611,003-159,327,017 MKLN1, RPL26P23, 887 more genes
    nsv3918979copy number variation1nstd102humanPathogenic GRCh37 chr7: 115,099,069-159,118,507 , NCBI36 chr7: 114,886,305-158,811,268 , GRCh38 chr7: 115,459,015-159,325,817 MKLN1, ABCF2, 844 more genes
    nsv3917337copy number variation1nstd102humanPathogenic GRCh38 chr7: 121,863,759-159,335,865 , NCBI36 chr7: 121,291,049-158,821,316 , GRCh37 chr7: 121,503,813-159,128,555 MKLN1, INSIG1-DT, 776 more genes
    nsv4349183copy number variation1nstd102humanPathogenic GRCh37 chr7: 128,312,450-159,119,220 , GRCh38.p12 chr7: 128,672,396-159,326,530 MKLN1, LOC105375582, 686 more genes
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