jakmip2[All Fields] AND 1[has_clinical] - dbVar

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Number of Variants: 20

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv3889848	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 17,628,741-176,575,720 , GRCh38.p12 chr5: 17,628,632-177,148,719	JAKMIP2, MEGF10, 2080 more genes
nsv3884357	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr5: 86,400,000-154,000,000 , GRCh38.p12 chr5: 87,104,183-154,620,440	JAKMIP2, TXNDC15, 962 more genes
nsv3912937	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 105,955,289-155,551,397 , NCBI36 chr5: 105,983,188-155,483,975 , GRCh38 chr5: 106,619,588-156,124,387	JAKMIP2, LINC01023, 783 more genes
nsv3878447	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 141,113,273-149,154,835 , GRCh38.p12 chr5: 141,733,706-149,775,272	JAKMIP2, LOC107986458, 111 more genes
nsv3918033	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr5: 145,197,355-148,541,511 , NCBI36 chr5: 144,557,111-147,901,267 , GRCh37 chr5: 144,576,918-147,921,074	JAKMIP2, LOC100288484, 50 more genes
nsv3886374	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 13,648-180,905,029 , GRCh38.p12 chr5: 13,648-181,478,028	JAKMIP2, LOC105374618, 2499 more genes
nsv3871533	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 25,328-180,693,344 , GRCh38.p12 chr5: 25,329-181,266,343	JAKMIP2, PCDHGC5, 2492 more genes
nsv3875235	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr5: 113,577-180,719,789 , GRCh38.p12 chr5: 113,462-181,292,788	JAKMIP2, SPEF2, 2490 more genes
nsv3874238	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 106,716,357-180,687,338 , GRCh38.p12 chr5: 107,380,656-181,260,337	JAKMIP2, PJA2, 1228 more genes
nsv3878636	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 130,125,085-157,574,910 , GRCh38.p12 chr5: 130,789,392-158,147,902	JAKMIP2, LOC100288484, 551 more genes
nsv3923414	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 130,196,621-154,701,371 , NCBI36 chr5: 130,224,520-154,681,564 , GRCh38 chr5: 130,860,928-155,321,811	JAKMIP2, HNRNPA3P7, 514 more genes
nsv3914009	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr5: 129,211,386-152,713,299 , GRCh38 chr5: 129,847,794-153,353,546 , GRCh37 chr5: 129,183,487-152,733,106	JAKMIP2, UQCRQ, 489 more genes
nsv3914878	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr5: 146,520,648-163,194,778 , GRCh37.p13 chr5: 146,540,455-163,262,200 , GRCh38.p12 chr5: 147,160,892-163,835,194	JAKMIP2, LOC105378231, 247 more genes
nsv3924856	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr5: 140,449,756-148,890,434 , GRCh37 chr5: 140,469,572-148,910,241 , GRCh38 chr5: 141,089,988-149,530,678	JAKMIP2, CTB-99A3.1, 160 more genes
nsv3884275	copy number variation	1	nstd102	human	Likely benign	GRCh37 chr5: 94,844,077-178,830,410 , GRCh38.p12 chr5: 95,508,373-179,403,409	JAKMIP2, LOC107986368, 1258 more genes
nsv4436202	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr5: 14,685,137-149,511,942 , GRCh38.p12 chr5: 14,685,028-150,132,379	JAKMIP2, RNU1-150P, 1757 more genes
nsv6637095	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr5: 147,060,274-147,304,443 , GRCh38.p12 chr5: 147,680,711-147,924,880	JAKMIP2, LOC100288484, 5 more genes
nsv4728780	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr5: 147,088,554-147,321,173 , GRCh38.p12 chr5: 147,708,991-147,941,610	JAKMIP2, SPINK1, 5 more genes
nsv3912593	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr5: 332,389-180,837,866 , GRCh37.p13 chr5: 279,389-180,905,260 , GRCh38.p12 chr5: 279,274-181,478,259	JAKMIP2, LOC105378993, 2492 more genes
nsv4457090	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr5: 140,424,333-148,985,999 , GRCh38.p12 chr5: 141,044,748-149,606,436	JAKMIP2, PCDHGC4, 165 more genes

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Items: 20

Number of Variants: 20

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