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Items: 1 to 20 of 23

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3893728copy number variation1nstd102humanBenign GRCh37 chr7: 90,111,744-90,166,905 , GRCh38.p12 chr7: 90,482,430-90,537,591 PTTG1IP2
    nsv3913502copy number variation1nstd102humanLikely benign NCBI36 chr7: 89,892,603-90,065,438 , GRCh37 chr7: 90,054,667-90,227,502 , GRCh38 chr7: 90,425,353-90,598,188 PTTG1IP2, CDK14
    nsv4676095copy number variation1nstd102humanUncertain significance GRCh37 chr7: 90,128,713-90,625,015 , GRCh38.p12 chr7: 90,499,399-90,995,700 PTTG1IP2, TVP23CP1, 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 PTTG1IP2, 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 PTTG1IP2, LOC107986817, 2014 more genes
    nsv3914094copy number variation1nstd102humanPathogenic GRCh38 chr7: 84,002,634-95,228,883 , GRCh37 chr7: 83,631,950-94,858,195 , NCBI36 chr7: 83,469,886-94,696,131 PTTG1IP2, LINC03017, 121 more genes
    nsv3894780copy number variation1nstd102humanPathogenic GRCh37 chr7: 10,704-159,122,532 , GRCh38.p12 chr7: 10,704-159,329,842 PTTG1IP2, RNU6-565P, 2684 more genes
    nsv4455091copy number variation1nstd102humanPathogenic GRCh37 chr7: 10,365-159,119,707 , GRCh38.p12 chr7: 10,365-159,327,017 PTTG1IP2, RPL23AP51, 2684 more genes
    nsv3909087copy number variation1nstd102humanPathogenic GRCh37 chr7: 44,935-159,126,310 , GRCh38.p12 chr7: 44,935-159,333,620 PTTG1IP2, MNX1-AS2, 2682 more genes
    nsv3908592copy number variation2nstd102humanPathogenic GRCh37 chr7: 43,361-159,119,707 , GRCh38.p12 chr7: 43,361-159,327,017 PTTG1IP2, TRGV3, 2682 more genes
    nsv6313801copy number variation1nstd102humanPathogenic GRCh37 chr7: 77,821,356-93,340,137 , GRCh38.p12 chr7: 78,192,039-93,710,825 PTTG1IP2, SOCS5P1, 140 more genes
    nsv5381780copy number variation1nstd102humanPathogenic GRCh37 chr7: 87,477,185-100,333,327 , GRCh38.p12 chr7: 87,847,870-100,735,704 PTTG1IP2, ARPC1A, 265 more genes
    nsv6315223complex substitution1nstd102humanPathogenic GRCh37 chr7: 43,360-159,119,707 , GRCh38.p12 chr7: 43,360-159,327,017 PTTG1IP2, AOC1, 2682 more genes
    nsv4352523inversion1nstd102humanPathogenic GRCh37 chr7: 20,954,043-114,556,605 , GRCh38.p12 chr7: 20,914,424-114,916,550 PTTG1IP2, ACHE, 1532 more genes
    nsv3917092copy number variation1nstd102humanLikely pathogenic NCBI36 chr7: 86,846,728-91,199,124 , GRCh37 chr7: 87,008,792-91,361,188 , GRCh38 chr7: 87,379,476-91,731,873 PTTG1IP2, CDK14, 44 more genes
    nsv3920135copy number variation1nstd102humanLikely benign NCBI36 chr7: 88,030,801-89,950,219 , GRCh37.p13 chr7: 88,192,865-90,112,283 , GRCh38.p12 chr7: 88,563,550-90,482,969 PTTG1IP2, LOC107986816, 20 more genes
    nsv3895021copy number variation1nstd102humanUncertain significance GRCh37 chr7: 90,054,667-91,313,448 , GRCh38.p12 chr7: 90,425,353-91,684,133 PTTG1IP2, FZD1, 7 more genes
    nsv6634332copy number variation1nstd102humanUncertain significance GRCh37 chr7: 113,371-159,042,325 , GRCh38.p12 chr7: 113,371-159,249,635 PTTG1IP2, RRBP1P1, 2680 more genes
    nsv3873500copy number variation1nstd102humanUncertain significance GRCh37 chr7: 73,591,993-93,683,437 , GRCh38.p12 chr7: 74,177,663-94,054,125 PTTG1IP2, LOC645324, 242 more genes
    nsv4675401copy number variation1nstd102humanUncertain significance GRCh37 chr7: 88,533,008-90,192,559 , GRCh38.p12 chr7: 88,903,694-90,563,245 PTTG1IP2, LOC101927446, 15 more genes
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